Arranta Bio

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Senior Accountant will be a key member of the Arranta's finance team, reporting to the Corporate Controller. This position will be critical in growing the accounting function and supporting a Big Four audit. ESSENTIAL JOB FUNCTIONS • Manage general ledger activity including: GL postings, account reconciliations, and interaction with business to ensure all monthly activity booked to Microsoft Dynamics ERP • Key contributor in the monthly and quarterly close and financial reporting process • Contributes to standardization of accounting process and policy at Arranta • Work closely with the facilities team and the Controller to ensure new and existing lease population is in compliance with ASC 842 leasing standard • Contributes to standardization of accounting process and policy at Arranta specifically relating to cash, prepaid/accrual, fixed asset, internally developed software and assist with inventory process • Interfaces with auditors during annual financial audit Experience and Skills EDUCATION AND/ OR EXPERIENCE • Bachelor's degree in Accounting • CPA certification preferred • 3-5 years experience in accounting roles with demonstrated growth • Big Four experience a plus • Proficient Microsoft Dynamic user • Knowledge of Sarbanes Oxley and SEC reporting a plus • Team player and self-starter with the ability to act autonomously • Solid business, accounting, and financial experience • Strong attention to detail • Excellent financial analysis experience • Strong time management and organizational skills • Able to manage multiple priorities and demonstrate self-control • Timely and accurate completion of tasks • Proven ability to work with professional discretion and confidential information • Advanced desktop application experience Microsoft Power point, Excel, and Word PHYSICAL DEMANDS The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE. Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are Agile, Leading, Innovating, Value Creating, and Engaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY This position supports functions including but not limited to: drafting of experimental plans, execute on own and suggested experimental designs, research literature to improve on methods and techniques, lead defined projects, independently pursue defined goals as well as take initiative in maintenance and troubleshooting of equipment, and sourcing materials and supplies, while meeting deadlines. The Employer may ask the Employee to carry out other reasonable duties as required. ESSENTIAL RESPONSIBILITIES • Preparation of media broth and media agar • Development and optimization of custom media • Fermentation • Culturing of bacteria in media agar and media broth • Plate streaking techniques • Fluorescent microscopy • Perform focused and systematic execution of laboratory experiment and assays • Perform data interpretation on experiments and assays conducted • Maintain and troubleshoot lab equipment • Prepare spreadsheets and reports • Research literature • Develop and improve methods and techniques • Bacterial cell banking Lyophilization Experience and Skills EDUCATION AND/ OR EXPERIENCE A bachelor's degree, with a strong interest in the life sciences, with 0-3 years' work experience in an industrial lab. Ability to plan and execute assigned tasks in a way that ensures efficient, thorough and organized execution, in a timely manner, is required. Ability to effectively research literature and other sources to improve on methods, lab processes, laboratory instrumentation, or experimental designs. Capable to interact and work with other team members to ensure high team productivity. Ability to work in cGMP environment is required Experience working within a quality system is preferred Knowledge of environmental and safety requirements is preferred PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is not required to travel The employee will be required to communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Head of Supply Chain directs all facets of supply chain and logistics supporting uninterrupted manufacturing of commercial microbiome and plasmid products at Arranta Bio's state-of-the-art manufacturing facility in Watertown, MA. He/She is accountable for building, maintaining, and continuously improving a highly effective supply chain system and workforce, driving activity to achieve the desired departmental, site, and company outcomes, and ensuring the highest standards of workplace safety and product quality are adhered to. The Head of Supply Chain provides direct leadership for material and production planning, warehousing/inventory control, and logistics, is a member of the Site Leadership Team, and is a key value stream leader ensuring uninterrupted supply of materials and finished product for Arranta Bio's clients. ESSENTIAL JOB FUNCTIONS * Identify and develop talent to produce a world class team consistent with the Arranta culture * Establish programs, practices, and processes to drive a high-performance and engaged workforce across areas such as Safety, Quality, Delivery, and Cost * Lead development of robust, cost effective manufacturing and supply chain strategies to enable uninterrupted supply of microbiome and plasmid products * Responsible for leading the Supply Chain Organization. Manage day to day operations to ensure departmental commitments and deliverables are achieved. This involves resource oversight, planning, delegation, prioritization, collaboration, etc. * Oversee the total inventory management process including but not limited to: weekly cycle counts, full physical inventory counts, posting counts, confirming tolerance ranges, recording variances, generating Zero Reports, performing inventory investigations when needed or required. * Maintain warehouse and logistics Operations (including general shipping, receiving, and freight management) to ensure compliance with cGMP requirements, standard operating procedures, guidelines, and policies. Assure compliance with federal, state, and local regulations as well all site safety requirements. * Encourage and enforce a culture of compliance regarding Safety, EH&S, Quality standards as required by cGMPs or other Health Authority' regulations, and company standards / policies. * Ensure adequate resource is dedicated to correcting important or critical issues via personal involvement, delegated resources, and/or appropriate escalation * Ensures awareness and compliance with Health authority regulations. * Ensures adequate training (skills-based, cGMP and Safety) of staff within department, to support commercial production and Pharmaceutical Development needs through highly competent staff * Participates in Regulatory Audits * Attend and/or lead internal and client project meetings. Work with internal stakeholders in manufacturing, process development, process sciences, project management etc. to facilitate successful project and customer management Experience and Skills Education and Experience * B.S. and/or advanced degree in related field with 10+ years of Supply Chain, industry, experience in cGMP environment * 10+ years of proven management experience * Minimum of 10+ years experience in biotechnology/pharmaceutical manufacturing practices, guidelines, management practices, cGMP knowledge, and production and planning operations * ISM, APICS, CSCMP, or Supply Chain Degree desired * General Warehouse Operations (inventory control, shipping, receiving, ERP, lift truck, etc.) * Transportation knowledge is a must * Hazardous Materials (Certification: IATA and 49CFR) * OSHA warehouse requirements * Manufacturing, inventory, and resource Information Systems know-how and experience in a high growth setting * Ability to work by influencing peers and their reports and gain their cooperation. * Strong people management and organizational skills; ability to prioritize and manage through complex processes/projects. * Strong interpersonal and communication skills PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. * The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. * The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. * Specific vision abilities required by this job include close vision, and ability to adjust focus. * In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. * Communicate using telephone and e-mail. BENEFITS Arranta Bio is an Equal Opportunity Employer.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Sr. Financial Analyst will be a key member of the Arranta's financial team, reporting to the Head of FP&A. This position is responsible for the day-to-day financial reporting, analysis and forecasting of our Massachusetts Manufacturing Site and will be a key business partner to the Site Head and the overall Site Leadership Team. This role will require the successful candidate to work seamlessly with internal teams, across different functions and levels of the organization, to manage the financials of a complex biologics manufacturing Site while being comfortable with varying levels of process sophistication. In addition, the successful candidate will also have the opportunity to play a key role in the partnership with Thermo Fisher and expand his / her responsibilities as the business continues to grow. ESSENTIAL JOB FUNCTIONS Reporting & Analysis: P&L Reporting by Global Business Unit with detailed analysis of Trial Balance elements. Cost Center Reporting for Site Functions Cash Flow & CapEx Reporting & Analysis Drive process improvement in Reporting through creation of self-service Dashboard Reporting for the Site LT Support the roll-out & implementation of Site Operations Review Support the Overall Consolidation of Arranta Bio Financials as needed Implement Early Warning process for Sales & Cost in Massachusetts Partner with Accounting to ensure efficient and accurate monthly close Forecasting: Monthly Sales & Cost Landings 12 Month Rolling Forecasting Partner w. HR and Site LT to accurately forecast Headcount Support the internal S&OP process Budgeting: Lead the Annual Operating Plan construction, review and approval for Massachusetts Site. Support the overall Arranta Bio Annual Operating Plan consolidation & review process as needed. Ad-hoc: Support evaluation of Capital investments for the Site as needed Support the business partnership with Thermo Fisher Drive Process alignment between MA & FL with regards to reporting & forecasting requirements Drive continuous improvement in rereporting and forecasting Partner with Accounting to ensure Experience and Skills EDUCATION AND/ OR EXPERIENCE Bachelor's degree in Finance or Accounting 5-7 years' experience in Finance roles with demonstrated growth Strong ERP background Proven Business Partnering experience & strong communication skills Previous Mfg Site Finance experience a plus Advanced desktop application experience Microsoft Power point, Excel, and Word Proven ability to work with professional discretion and confidential information PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Warehouse Senior Manager leads the warehouse operations team ensuring safe, GMP compliant execution and management of operations to support GMP manufacturing, including but not limited to; Watertown site inventory control, warehouse space allocation, material handling, receiving, stocking, picking, issuing and product shipping. Scope also includes developing strategies for risk remediation and mitigation, warehouse manager ensures strategic goals, policies and procedures of the organization are understood & followed when carrying out functions. Recruits, coaches, trains, and motivates team members to successfully perform their job and promotes individual development through mentoring and both personal and team growth. ESSENTIAL JOB FUNCTIONS Develops and implements the overall strategy that outlines the specific priorities and individual responsibilities needed to accomplish the groups broad functions, (inventory control, material handling, shipping and receiving, development and tracking of KPI's ). Ensure safe warehouse operations Ensures timely receiving, stocking, picking, issuing, and shipping of materials Ensures compliance with Quality Systems · Track performance by leading daily warehouse huddle (SQDCP) Timely investigation and resolution of issues using lean problem-solving tools and techniques (eg RCA) Collaborates with PD, Manufacturing, Quality for the execution of warehouse related activities. Provide GMP manufacturing support related to warehouse items Write, review, and approve Standard Operating Procedures Establish and maintain appropriate stocking levels Develop and manage cycle count program and physical inventory activities Ensure appropriate training and operation of material handling equipment Experience and Skills EDUCATION AND/ OR EXPERIENCE Bachelor's Degree in Business, Supply Chain, Operations Management, or related field 5+ years of related management experience in a GMP setting, preferably Lean Inventory Control experience (cycle counts, physical inventories) MS Excel, Project, ERP systems (MS Dynamics a plus) Proficiency in training/mentoring, ability develop warehouse team members. Able to serve as a contributing partner on the Leadership Team. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY Arranta Bio, LLC is a dynamic Biome and Plasmids contract development and manufacturing organization that is looking for leaders to bring the highest quality processes, products and testing to our clients. Our staff members are committed to making a difference in our organization, for our client partners and the patients we serve. We seek individuals with proven competencies and strong character to help lead our organization now and into the future. The Maintenance Planner will report directly to the site Sr Manager of Facilities and Engineering. The Maintenance Planner will be responsible for the daily planning and scheduling of maintenance and calibration activities at Arranta Bio's Watertown, MA sites. The focus of the position is to ensure the on-time completion of maintenance and calibration activities. In operations, the Maintenance Planner is responsible for the daily coordination of activities between the maintenance organization, manufacturing, QC and PD. The planner will also manage scheduling services associated with the facility, labs, and grounds. (S)he works with the site Engineering team, Manufacturing, QC, PD, and QA to ensure assigned maintenance items are being completed in a timely manner. (S)he may be asked to add and manage assets in the CMMS system, as well as develop reports and report on metrics related to the completion of maintenance and calibration activities. The position involves close collaboration with Manufacturing, Manufacturing Sciences, Quality Assurance, Quality Control, and other Engineering teams to complete all responsibilities. KEY CHARACTERISTICS Previous proficient experience with CMMS software system(s) Knowledge of generally accepted building and electrical codes in compliance with the Town of Watertown and the State of Mass. including but not limited to NEC, NFPA 70, etc. Knowledge of OSHA and EPA regulations Strong technical documentation review and revision experience Experience with single-use technologies Strong ability to work independently Comfortable supporting multiple concurrent issues Experience and Skills EDUCATION AND/ OR EXPERIENCE Minimum of 5 years of experience in the facilities/engineering/manufacturing environment Direct experience supporting building facilities and utility systems within a manufacturing/production environment is desirable. Experience managing services, including lab services, janitorial services, security, and food/beverage services. Understanding of local and state regulations and permitting. Experience with Blue Mountain RAM or other CMMS. Strong interpersonal and communications skills; written and oral PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. • The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. • The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. • Specific vision abilities required by this job include close vision, and ability to adjust focus. • In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. • Communicate using telephone and e-mail

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE. Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are Agile, Leading, Innovating, Value Creating, and Engaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Head of Facilities will provide overall technical expertise and leadership to develop and implement the facilities and maintenance strategies for a new clinical cGMP manufacturing, warehouse, lab, and office facility located in Gainesville, FL. He/She is accountable for building, maintaining, and continuously improving a highly effective facilities workforce, driving activity to achieve the desired departmental, site, and company outcomes, and ensuring the highest standards of workplace safety and product quality are adhered to. The position oversees all aspects of the facilities management of Arranta's early process development and clinical GMP drug substance and drug product microbiome live biotherapeutic manufacturing facility, lab, warehouse, and office facilities in Florida, FL. The initial work will include the building of the systems, procedures and a team of skilled professionals to ensure a superior level of services in the areas of building systems, maintenance and repair, metrology, and custodial functions such as grounds and general maintenance. Specialty systems include the Building Management System (BMS), HVAC, water and specialty gas systems, alarm monitoring, emergency power and other critical systems to support a regulated laboratory and manufacturing environment. ESSENTIAL RESPONSIBILITIES • Identify and develop talent to produce a best-in-class team consistent with the Arranta mission and culture • Development and maintenance of standard specifications and procedures for maintenance of plant mechanical and production systems and equipment. (Preventative maintenance programs, calibration program, etc. supporting facility start-up and ongoing continuous improvement). • Collaborates with PD, Manufacturing, Quality for the execution of all equipment set-up, qualification, validation, maintenance, calibration, and metrology-related activities. • Work closely with outside contractors to ensure that contracted maintenance services are performed to satisfactory specifications. • Provides technical assistance and training to individuals to assure compliance with cGMP guidelines and written procedures. • Promptly address plant/equipment challenges. • Direct critical and facility equipment changes. • Specify, review and approve purchases of equipment and service. • Assist in specifying conceptual and detail design requirements for plant expansions and improvement projects. • Direct the activities of maintenance, construction, and other vendor/contractors. • Responsible for the annual Facilities Operational Budget. Is accountable for effective cost management and cost control, working proactively to maintain approved departmental and project budgets, and provide budgetary forecasts as required. Integrates budgets with the Chief Financial Officer Experience and Skills EDUCATION AND/ OR EXPERIENCE • B.S. in Engineering or related field • 7+ years of related experience in a GMP setting • Excellent communication skills, written and verbal • Team player with the ability to influence others, inside and outside the organization. • Ability to handle multiple priorities simultaneously • Flexibility in problem solving • Ability to work independently and cross-functionally in a dynamic environment. • Strong time management and prioritization skills to manage multiple projects with critical, FDA enforced, deadlines and tight budgets. • A broad understanding of Facilities-related subject matters is required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. • The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. • The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. • Specific vision abilities required by this job include close vision, and ability to adjust focus. • In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. • Communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE. Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are Agile, Leading, Innovating, Value Creating, and Engaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Head of Facilities will provide overall technical expertise and leadership to develop and implement the facilities and maintenance strategies for a new commercial cGMP manufacturing, warehouse, lab, and office facility located in Boxborough, MA. He/She is accountable for building, maintaining, and continuously improving a highly effective facilities workforce, driving activity to achieve the desired departmental, site, and company outcomes, and ensuring the highest standards of workplace safety and product quality are adhered to. The position oversees all aspects of the facilities management of Arranta's commercial plasmid and microbiome manufacturing facility, lab, warehouse, and office facilities in Boxborough, MA. The initial work will include the building of the systems, procedures and a team of skilled professionals to ensure a superior level of services in the areas of discreet and complex building systems, maintenance and repair, metrology, and custodial functions such as grounds and general maintenance. Specialty systems include the Building Management System (BMS), HVAC, water and specialty gas systems, alarm monitoring, emergency power and other critical systems to support a regulated laboratory and manufacturing environment. Identify and develop talent to produce a world class team consistent with the Arranta culture Development and maintenance of standard specifications and procedures for maintenance of plant mechanical and production systems and equipment. (Preventative maintenance programs, calibration program, etc. supporting facility start-up and ongoing continuous improvement). Collaborates with PD, Manufacturing, Quality for the execution of all equipment set-up, qualification, validation, maintenance, calibration, and metrology-related activities. Work closely with outside contractors to ensure that contracted maintenance services are performed to satisfactory specifications. Provides technical assistance and training to individuals to assure compliance with cGMP guidelines and written procedures. Promptly address plant/equipment challenges. Direct critical and facility equipment changes. Specify, review and approve purchases of equipment and service. Start up and commissioning of utility infrastructure. Assist in specifying conceptual and detail design requirements for plant expansions and improvement projects. Direct the activities of maintenance, construction, and other vendor/contractors. Responsible for the annual Facilities Operational Budget. Is accountable for effective cost management and cost control, working proactively to maintain approved departmental and project budgets, and provide budgetary forecasts as required. Integrates budgets with the Chief Financial Officer Hire, recruit, coach, and train employees within the Facilities department Build and lead a facility team Set short-term and long-term goals for the facilities function that are aligned with Arranta's goals. Continuously assess and ensure the appropriate facilities structure is in place to support growth. Identify gaps and ensure the proper hiring and development of employees with the support of Human Resources. Set expectations, provide feedback and coaching, and take necessary action to ensure appropriate performance and goal attainment. B.S. in Engineering or related field Experience and Skills EDUCATION AND/OR EXPERIENCE 10+ years of related experience in a GMP setting Excellent communication skills, written and verbal Team player with the ability to influence others, inside and outside the organization. Ability to handle multiple priorities simultaneously Flexibility in problem solving Ability to work independently and cross-functionally in a dynamic environment. Strong time management and prioritization skills to manage multiple projects with critical, FDA enforced, deadlines and tight budgets. A broad understanding of Facilities-related subject matters is required. BENEFITS Arranta Bio is an Equal Opportunity Employer.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY Arranta Bio, LLC is a dynamic Biome and Plasmids contract development and manufacturing organization that is looking for leaders to bring the highest quality processes, products and testing to our clients. Our staff members are committed to making a difference in our organization, for our client partners and the patients we serve. We seek individuals with proven competencies and strong character to help lead our organization now and into the future. ESSENTIAL JOB FUNCTIONS Responsible for MES systems (Emerson, Allen Bradley, and Siemens). Scope includes developing and implementing an automation roadmap based on organizational requirements and industry best practices. This will include balancing the long-term goals for the manufacturing organization against the short-term needs and resources available. Individual will be part of an experienced team of engineers working closely with groups such as manufacturing, quality assurance, quality control and validation. The individual will also be responsible for aligning/coordinating capabilities across sites within the company while ensuring that the capabilities of the Watertown site meets all regulatory requirements necessary for commercial manufacturing. Experience and Skills EDUCATION AND/ OR EDUCATION B.S. in Automation, Electrical, Chemical, Mechanical Engineering, Computer Science with 13+ years of experience in the biotech engineering/manufacturing environment or equivalent experience Experience with people or project management. Candidate must also have the capability to define and set technical direction for the automation system. Experience with DCS and/or PLC coding including but not limited to DeltaV, Allen Bradley PlantPAx, and Siemens. Experience with BMS system such as JCI/Metasys Understanding of regulatory FDA Part 11 and European Annex 11 requirements and experience applying these standards to the qualification of automation systems. Familiarity with systems such as ESXi, Syncade, OSI PI, Infobatch and Labwatch Understanding of instrumentation, electrical standards, and local requirements Strong interpersonal and communications skills; written and oral Advanced understanding of applicable regulatory requirements Strong technical documentation review and revision experience DCS/PLC/Automation system installation and support Basic understanding of network architecture Working with both hands-on and remote based staff Strong ability to work independently Comfortable supporting multiple concurrent issues

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Material Handler will perform and document daily warehouse/inventory operations safe and efficient manner within a regulated (cGMP) environment. Through cross training, they will become a subject matter expert in multiple areas within materials management/supply chain department such as shipping and receiving, GMP raw material inventory control, cell bank storage and cold chain of custody, logistics and distribution. ESSENTIAL JOB FUNCTIONS Follow cGMP procedures, retrieve documents from the document management system, complete cGMP documentation using good documentation practices Identify gaps in procedures. Collaborate with the management team effectively to improve procedures/processes and write new Initiate and close quality exceptions such as deviations expeditiously Work effectively with a cross functional team to complete investigations as necessary Interact with a wide variety of professionals from inside and outside the organization such as consultants, regulatory agencies, and vendors Mentor and train less junior associates in materials management and warehouse functions Work safely and effectively in areas such as shipping and receiving, GMP raw materials, inventory control, cell bank storage, logistics and distribution Safely operate all motorized equipment including forklift truck, electric pallet jacks, lifts, and company vehicles Alarm response and on-call responder Experience and Skills EDUCATION AND/ OR EXPERIENCE High school diploma or equivalent 2-5 years' experience in a related or equivalent field is required, biotech and/or pharma GMP experience preferred This role will require lifting, bending and climbing. This role will require the use of ladders, rigging and portable lifting equipment. The ability to safely utilize pallet jacks and fork trucks is required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 20 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY Arranta Bio seeks a night shift Senior Bio-Manufacturing Engineer who brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be independent, goal-oriented, flexible, and able to work efficiently across multiple projects. We are searching for enthusiastic, and innovative individuals with a good understanding of Change Controls, Quality Investigations, and familiar with Upstream and Downstream biomanufacturing principles. ESSENTIAL JOB FUNCTIONS Lead to completion of project milestones and organize own work to meet project task deadlines. Provide written and verbal updates to supervisors or other department managers Train and lead Manufacturing Associates Use operational and technical expertise to assist in troubleshooting activities, technology transfer and start-up activities. Monitor the technical documentation for the production and processes approval. Ensure all production equipment and systems are in compliance with (Current) Good Manufacturing Practices. Manage execution of relevant process activities by following established Standard Operating Procedures. Perform process monitoring and data analysis, and data preparation for presentation in several forums including project team meeting Effectively maintain good communication and collaborate with cross-functional colleagues and external partners for successful execution/completion of projects. Participate in the tech transfer and scale-up of developed processes to pilot and/or GMP manufacturing. Work on problems of diverse scope (bridging upstream and downstream processes, manufacturing) the development schedule Evaluate functional strengths and developmental areas a team with the ability to focused on continuous improvement Experience and Skills EDUCATION AND/ OR EXPERIENCE 4+ Bachelor's Degree 3+ years Manufacturing experience with demonstrated progression from Associate I-III Working knowledge of Microsoft Outlook, Word and Excel required. Effective verbal and written communication skills Mechanical knowledge and the use of hand tools Demonstrated ability to train and coach others Experience with Six Sigma or other operational excellence programs Ability to handle multiple tasks while remaining focused Reliable, dependable, and organized PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is required to work overnight 12 hour night shifts The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The night shift Manufacturing Supervisor will supervise daily cGMP manufacturing activities for plasmid products including master cell bank production, final fill operations, as well as upstream, purification, media/buffer production, and general suite/operational readiness activities. The Cell Banking and Final Fill Manufacturing Supervisor is responsible for providing direction, training and development for the Manufacturing Associates I-III and Senior Associates. ESSENTIAL JOB FUNCTIONS Supervise microbial cell banking and final fill, as well as operations associated with the seed train, fermenter operation, harvest/clarification activity, and purification of plasmid DNA in a commercial cGMP environment Ensure proper documentation of all activities in Batch Records, Logbooks, Forms, etc. and electronic interfaces. Ensure the production schedule is being adhered to by ensuring proper personnel, materials and equipment are available on time. Provide written and verbal updates to Manufacturing Leadership and department managers Maintain the highest standards of workplace Safety and product quality Ensures verbal and written procedures are followed and appropriate production documentation is accurately completed. Identifies, escalates and documents events and deviations from normal operation; active participant in investigations, driving to Root Cause identification and completion. Authors and reviews SOPs and Batch Records, as required. Coordinate activities to ensure validation/revalidation, preventive maintenance programs, training, maintenance and safety programs are met. Meet predefined metrics related to manufacturing and related testing and facility operation. Meet with relevant QA department personnel to coordinate documentation reviews and audits. Strong commitment to continuous improvement Experience and Skills EDUCATION AND/ OR EXPERIENCE B.S. in Biology, Chemical Engineering or related field preferred. Minimum of 5 -10 years previous experience in a relevant position in GMP manufacturing in a Biopharmaceutical company. Experience in producing and maintaining Master Cell Banks, as well as Final Fill operations. Operational Excellence, such as 6S, experience a plus · 3+ years in a leadership role Working knowledge of Microsoft Outlook, Word and Excel required. Ability to work well with others in a collaborative team environment. Able to work in a rapidly changing climate - reacts well to change Team player Ability to handle multiple tasks while remaining focused Reliable, dependable, and organized PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is required to work overnight 12 hour night shifts The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The night shift Manufacturing Associate I-III will perform daily cGMP manufacturing for plasmid products including upstream, purification, media/buffer production, and general suite/operational readiness activities. ESSENTIAL JOB FUNCTIONS Perform basic to complex activities in seed train, fermenter operation, harvest/clarification activity, and purification of plasmid DNA in a commercial cGMP environment Preparation of media and buffers Documentation of all activities in Batch Records, Logbooks, Forms, etc. and electronic interfaces Maintain the highest standards of workplace Safety and product quality Follows verbal and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation. Identifies, escalates and documents events and deviations and subtle variances that deviate from normal operation; participate as needed in investigations. Demonstrates ability to troubleshoot basic mechanical operations. Work in accordance with site and company EHS programs. Work in accordance with regulations, detailed protocols, Batch Records, SOPs and Work Instructions Strong commitment to continuous improvement Experience and Skills EDUCATION AND/ OR EXPERIENCE High School, Technical Degree OR B.S. in Biology, or related field preferred. Operational Excellence, such as 6S, experience a plus Working knowledge of Microsoft Outlook, Word and Excel required. Good laboratory skills and excellent record keeping, including GDP, is required. Ability to work independently and stay on task in a fast-paced environment without direct supervision. Ability to work well with others in a collaborative team environment. Regular and reliable performance and attendance required. Preferred experience with anaerobic culture techniques Able to work in a rapidly changing climate - reacts well to change Team player Ability to handle multiple tasks while remaining focused Reliable, dependable, and organize PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is required to work overnight 12 hour night shifts The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Manager, Plasmid Planning, maintains a holistic view of plasmid manufacturing activity for the operating site, ensuring manufacturing planning functions as the "control tower" providing all planning and reporting required to enable operational success; maximizing OTIF performance and customer satisfaction by managing the creation, maintenance, and evaluation of all manufacturing plans, and proposing and escalating required management interventions addressing constraints and trends across all facets of manufacturing planning and performance. This role leads site plasmid planning activity and is responsible for continuously assessing and improving the capability and robustness of all planning processes in a low volume, repetitive, make to order environment to effectively operate and minimize risk to the business while maximizing operational performance and stakeholder satisfaction throughout the site and network. Operates cross-functionally to actively shape and drive the development and execution of metrics, analyses, new process implementation, and process improvement. This is a managerial role for a single site and reports to the Head of Supply Chain ESSENTIAL JOB FUNCTIONS Develop, administer, maintain, and improve end-to-end manufacturing planning processes, including, but not limited to, supply planning, master scheduling, material and inventory planning, capacity planning, and operational reporting. Lead planning in the evolution from startup to a fully integrated systems approach, recognizing short and mid-term gaps and vulnerabilities, and mitigating associated risks by rapidly standing up and maturing planning processes. Develop and maintain planning and operational KPIs measuring the operating health of the site and its ability to meet short-term and ongoing customer expectations and financial objectives. Alert cross-functional stakeholders and the management chain of command to all observed issues, their potential implications, and formulate, drive and escalate required countermeasures as needed. Work collaboratively with Manufacturing, Process Development, and Technology Transfer; establishing schedules to meet contractual obligations and to create and maintain bills of materials for manufacturing, process development, and technology transfer campaigns. Monitor the manufacturing, process development, and technology transfer schedules as they relate to raw material inventory and consumption and ensure raw materials are procured and on-hand to ensure on-time delivery of production schedules. Collaborate daily with Manufacturing, Supply Chain, Quality Control, and Quality to resolve raw material issues, scheduling conflicts, inventory levels, and delivery requirements. Develop raw material supply and quality risk assessments for all BOM items, create risk mitigation plans for high-risk materials, and execute risk mitigation plans to ensure uninterrupted drug/material supply. Develop an inventory policy based on supply chain risk and manage demand forecasting, raw material and inventory planning, and raw material and safety stock levels to prevent manufacturing or development delays in a highly complex environment managing multiple BOMs, WIPs, and technology platforms. Work cross-functionally with manufacturing and process development to model various scenarios facilitating go/no-go decisions. Experience and Skills EDUCATION AND/ OR EXPERIENCE Bachelor's degree in Supply Chain, Operations, Business, Industrial Engineering, or related field; Master's degree in Supply Chain, Operations Management, or Business Administration (MBA) preferred Seven years of experience in supply chain or manufacturing planning and operations Five years of demonstrated people management experience Advanced knowledge in supply planning (Master Production Scheduling, Materials Requirement Planning, Capacity Planning) processes with demonstrated experience building, standing up, and maturing end-to-end manufacturing planning processes Advanced ERP skills; Microsoft Dynamics preferred, or Tier 1 experience in Oracle or SAP Advanced analytical skills using purpose-built statistical software, i.e., Minitab or JMP, Access, or Excel, including complex pivoting and data mining Certified in production and inventory management or supply chain management; APICS CPIM, CSCP, or ISM CPSM preferred Lean, Six Sigma, or Lean Six Sigma credentials preferred; green belt or higher Expertise functioning within a formal business management system such as Toyota, Danaher, Ingersoll Rand, Honeywell or similar structured methodology preferred Prior cGMP regulated experience in pharmaceutical or biotechnology industry a plus Manufacturing and supply chain acumen. Direct experience with a consistent record of demonstrating significant, quantifiable success and achievement in complex manufacturing and supply chain environments is essential. Business partner. Maintains a strong commercial orientation and a proven ability to partner with line managers and operating teams to drive and monitor performance and to develop strategic plans that elevate process and operational performance. Leadership presence. Comfortable being uncomfortable, consistently displaying sound judgment, and a passion for excellence, with a solution focus, promoting process improvement across the site. Ability to interact with the site and senior management in a manner that instills confidence and respect at all levels of the organization. Effectively Consumes Data. Good at identifying trends and interpreting data with a clear ability to connect the dots; understanding how behavior and decisions in any part of the system influence overall system dynamics. Examines scenarios from multiple perspectives, asks the right questions to gain additional insights, understands potential implications in a fact-based manner, and formulates and drives appropriate interventions and countermeasures. Acts with urgency. Instinctively takes the initiative while thoroughly understanding and operating in the context of the big picture, key drivers, and what we can accomplish; relentlessly pursues rapid improvement and excellence over a crawl toward perceived perfection. Owner's mentality. Embraces accountability and maintains an owner's mindset - takes action: see something, say something, do something; protects and promotes culture, protects and grows the business, and develops others. Attention to detail. Displays accuracy and precision in the creation of all deliverables and in carrying out all facets of responsibility. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY Arranta Bio seeks a night shift Bio-Manufacturing Engineer who brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be independent, goal-oriented, flexible, and able to work efficiently across multiple projects. We are searching for enthusiastic, and innovative individuals with a good understanding of Change Controls, Quality Investigations, and familiar with Upstream and Downstream biomanufacturing principles. ESSENTIAL JOB FUNCTIONS Contribute to completion of project milestones and organize own work to meet project task deadlines. Use operational and technical expertise to assist in troubleshooting activities, technology transfer and start-up activities. Monitor the technical documentation for the production and processes approval. Ensure all production equipment and systems are in compliance with (Current) Good Manufacturing Practices. Manage execution of relevant process activities by following established Standard Operating Procedures. Perform process monitoring and data analysis, and data preparation for presentation in several forums including project team meeting Effectively maintain good communication and collaborate with cross-functional colleagues and external partners for successful execution/completion of projects. Participate in the tech transfer and scale-up of developed processes to pilot and/or GMP manufacturing. Work on problems of diverse scope (bridging upstream and downstream processes, manufacturing Experience and Skills EDUCATION AND/ OR EXPERIENCE 4 years' experience + Bachelor's Degree Experience within the pharmaceutical industry Effective verbal and written communication skills Mechanical knowledge and the use of hand tools Demonstrated ability to train and coach others Experience with Six Sigma or other operational excellence programs PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is required to work overnight 12 hour night shifts The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Supply Chain Manager leads the warehouse operations team ensuring safe, GMP compliant execution and management of operations to support GMP manufacturing, including but not limited to; Watertown site inventory control, warehouse space allocation, material handling, receiving, stocking, picking, issuing and product shipping. Scope also includes developing strategies for risk remediation and mitigation, warehouse manager ensures strategic goals, policies and procedures of the organization are understood & followed when carrying out functions. Recruits, coaches, trains, and motivates team members to successfully perform their job and promotes individual development through mentoring and both personal and team growth. ESSENTIAL JOB FUNCTIONS Develops and implements the overall strategy that outlines the specific priorities and individual responsibilities needed to accomplish the groups broad functions, (inventory control, material handling, shipping and receiving, development and tracking of KPI's ). Ensure safe warehouse operations Ensures timely receiving, stocking, picking, issuing, and shipping of materials Ensures compliance with Quality Systems · Track performance by leading daily warehouse huddle (SQDCP) Timely investigation and resolution of issues using lean problem-solving tools and techniques (eg RCA) Collaborates with PD, Manufacturing, Quality for the execution of warehouse related activities. Provide GMP manufacturing support related to warehouse items Write, review, and approve Standard Operating Procedures Establish and maintain appropriate stocking levels Develop and manage cycle count program and physical inventory activities Ensure appropriate training and operation of material handling equipment Experience and Skills EDUCATION AND/ OR EXPERIENCE Bachelor's Degree in Business, Supply Chain, Operations Management, or related field 5+ years of related management experience in a GMP setting, preferably Lean Inventory Control experience (cycle counts, physical inventories) MS Excel, Project, ERP systems (MS Dynamics a plus) Proficiency in training/mentoring, ability develop warehouse team members. Able to serve as a contributing partner on the Leadership Team. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY Reporting to the Facilities and Maintenance Manager, this position will be responsible for HVAC, High Purity Water Systems (WFI), GMP facilities/utilities, and grey utilities supporting Arranta Bio's Plasmid and Microbiome Manufacturing Facility in Watertown, MA. This position will provide engineering support for utilities and HVAC to the campus, support the execution of day to day operations, projects and troubleshooting. This position will lead investigations relating to non-conformance events in partnership with Quality, IT, and Manufacturing. ESSENTIAL JOB FUNCTIONS Supervise and lead Plant Engineers responsible for MEP, HVAC, and I&C support for the Watertown Campus. Provide technical guidance, coaching, and work prioritization assistance with the Plant Engineers. Provide direct engineering support for the clean utilities including WFI generation, storage, and distribution and process gases. The engineer will provide technical support of grey utilities including chilled water, steam, boilers, and condensate systems, including the associated BMS controls. GMP HVAC support is to include expertise in clean room design, air distribution, HEPA filtration and certification, and pressure differential and pressure alarming strategies. Troubleshooting equipment to determine root cause of failure modes, owning Corrective/Preventative Actions and associated change controls, providing input into preventative maintenance plans, assessing change controls, and continuous improvement initiatives. Provide a high level of customer support to the Facilities and Manufacturing teams, the Senior Engineer must develop a deep knowledge of the utility and HVAC requirements of each of the manufacturing areas. The ability to collaborate cross-functionally with stakeholders to determine the best path forward to identified issues by balancing technical, compliance, and business objectives. The Senior Engineer needs to be able to drive results by owning and completing the subsequent projects including high quality technical writing within the required quality systems and meeting the project timelines to ensure the production schedule is not impacted. Drive results on multiple complex assignments simultaneously with minimal required direction from his/her supervisor, in addition to reviewing and guiding the work and performance of contractors. The Senior Engineer will have specific safety objectives to include proactively evaluating the safety of the operation of the utility and HVAC equipment and propose and implement safety improvements. The Senior Engineer must always work in a safe manner by adhering to all safety procedures and have a proactive safety mindset. The Senior Engineer will participate on project teams through all phases of engineering projects in the HVAC and utility areas including conceptual design, detailed design, equipment procurement, construction, installation, start up, commissioning, validation, and qualification of facilities and/or equipment. Experience and Skills EDUCATION AND/OR EXPERIENCE Applicant must have familiarity with biotechnology operations, including GMPs. Knowledge of clean room design, GMP HVAC, grey utilities, and GMP utilities. Excellent interpersonal and communication skills (verbal and written) are required. Expected to be able to present own work to peers and cross-functional managers and influence leadership decisions. Technical writing skills required. Must be able use his/her technical background to investigate issues using a structured problem-solving approach to determine true root cause and develop effective corrective and preventative actions. Must be able to be able to find true root cause and path forward for complex problems. Familiarity with Excel, Word, and PowerPoint are required, and basic statistical analysis techniques are preferred. Ability to interact well with other groups and must be able to take ownership of and follow through on assignments. Must be able to drive results on multiple complex assignments simultaneously with minimal required direction from his/her supervisor. Ability to represent Arranta Bio's interests, objectives and policies in a professional and responsible manner. Experience in large engineering capital projects is preferred. A minimum of eight years professional experience required in engineering, facilities or operations. A minimum of five years relevant experience in cGMP environment is desirable. BS in Chemical or Mechanical Engineering. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE. Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are Agile, Leading, Innovating, Value Creating, and Engaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY A strong individual contributor who possesses initiative, drive and takes pride in a job well done. The Specialist I will work alone occasionally and will need to demonstrate the ability to make informed decisions and be accountable for them. The Specialist I will be required to be agile and able to pivot priorities with short notice. ESSENTIAL RESPONSIBILITIES · Serve as the system administrator for the CMMS system - this responsibility will include data transfer into the CMMS from existing systems, developing preventive maintenance and calibration procedures, and asset identification and entry, and ongoing maintenance of the system. · Serve as the system administrator for the equipment monitoring systems - this will include the development of call lists, alarm parameters, and routine maintenance of the system. · Develop change controls, impact assessments, risk assessments and other equipment/systems related documents. · Develop, implement, and maintain spares inventory. · Manage projects as assigned. · Develop and analyze KPIs and reports for Facilities and Calibrations. · Manage and document calibrations for lab equipment. · Assist in preventive and corrective maintenance for lab equipment. · Perform accurate, relevant documentation of all work performed. · Provide input to management for improvement of processes, maintenance and calibration activities and procedures. Experience and Skills EDUCATION AND/ OR EXPERIENCE High School Diploma Previous Supervisory experience preferred Two to Five years' experience in a related or equivalent field is required. Solid foundation in the fundamentals of preventive and corrective maintenance. Solid foundation in the fundamentals of calibrations. Experience in 6S and Lean Manufacturing PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE. Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are Agile, Leading, Innovating, Value Creating, and Engaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY This position supports functions including but not limited to: drafting of experimental plans, execute on own and suggested experimental designs, research literature to improve on methods and techniques, lead defined projects, independently pursue defined goals as well as take initiative in maintenance and troubleshooting of equipment, and sourcing materials and supplies, while meeting deadlines. The Employer may ask the Employee to carry out other reasonable duties as required. ESSENTIAL RESPONSIBILITIES • Preparation of media broth and media agar • Development and optimization of custom media • Fermentation • Culturing of bacteria in media agar and media broth • Plate streaking techniques • Fluorescent microscopy • Perform focused and systematic execution of laboratory experiment and assays • Perform data interpretation on experiments and assays conducted • Maintain and troubleshoot lab equipment • Prepare spreadsheets and reports • Research literature • Develop and improve methods and techniques • Bacterial cell banking Lyophilization Experience and Skills EDUCATION AND/ OR EXPERIENCE A bachelor's degree, with a strong interest in the life sciences, with 0-3 years' work experience in an industrial lab. Ability to plan and execute assigned tasks in a way that ensures efficient, thorough and organized execution, in a timely manner, is required. Ability to effectively research literature and other sources to improve on methods, lab processes, laboratory instrumentation, or experimental designs. Capable to interact and work with other team members to ensure high team productivity. Ability to work in cGMP environment is required Experience working within a quality system is preferred Knowledge of environmental and safety requirements is preferred PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is not required to travel The employee will be required to communicate using telephone and e-mail.

ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and GMP manufacturing services to microbiome innovators within the pharmaceutical industry. Therapies focused on the human microbiome are exhibiting incredible potential towards revolutionizing disease etiology and associated medical treatments. Arranta Bio's mission is to build a world class organization which provides microbiome bio-pharmaceutical innovators with a single source of supply from early process development through clinical and commercial GMP finished product. WHO ARE WE Arranta hires people who are committed and passionate to the goal of bringing life enhancing products to patients. We want top talent who will render ideas and a relentless desire towards accomplishing our mission; when a job becomes a passion, it makes you feel ALIVE . Here at Arranta Bio, we embrace ALIVE - our core values that we live and breathe daily! We are A gile, L eading, I nnovating, V alue Creating, and E ngaging. We embrace our challenges as opportunities. We are empowered to think and act. We never settle; we strive to improve through purposeful creativity. We build aligned teams who learn, grow, and deliver. We are committed to building strong relationships. Are you ready to come ALIVE with a daring and intrepid team? Don't wait another minute; Apply today! JOB SUMMARY The Senior Accountant will be a key member of the Arranta's finance team, reporting to the Corporate Controller. This position will be critical in growing the accounting function and supporting a Big Four audit. ESSENTIAL JOB FUNCTIONS • Manage general ledger activity including: GL postings, account reconciliations, and interaction with business to ensure all monthly activity booked to Microsoft Dynamics ERP • Key contributor in the monthly and quarterly close and financial reporting process • Contributes to standardization of accounting process and policy at Arranta • Work closely with the facilities team and the Controller to ensure new and existing lease population is in compliance with ASC 842 leasing standard • Contributes to standardization of accounting process and policy at Arranta specifically relating to cash, prepaid/accrual, fixed asset, internally developed software and assist with inventory process • Interfaces with auditors during annual financial audit Experience and Skills EDUCATION AND/ OR EXPERIENCE • Bachelor's degree in Accounting • CPA certification preferred • 3-5 years experience in accounting roles with demonstrated growth • Big Four experience a plus • Proficient Microsoft Dynamic user • Knowledge of Sarbanes Oxley and SEC reporting a plus • Team player and self-starter with the ability to act autonomously • Solid business, accounting, and financial experience • Strong attention to detail • Excellent financial analysis experience • Strong time management and organizational skills • Able to manage multiple priorities and demonstrate self-control • Timely and accurate completion of tasks • Proven ability to work with professional discretion and confidential information • Advanced desktop application experience Microsoft Power point, Excel, and Word PHYSICAL DEMANDS The employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl. Specific vision abilities required by this job include close vision, and ability to adjust focus. In the performance of the duties of this job the employee is required to travel occasionally, drive a motor vehicle. Communicate using telephone and e-mail.