Help us change lives At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others. Position Overview The Maintenance Technician II, BAS Controls is responsible for installing, servicing, repairing, troubleshooting and preventive maintenance on all Exact Sciences' Building Automation System (BAS) control systems. This position is responsible for a wide range of equipment from large-scale commercial-grade HVAC systems to multi-zone systems that incorporate direct digital control (DDC), pneumatic, electronic, and/or programmable logic controls. This position is responsible for installation, operation, maintenance, service, and repair of direct digital control systems and control programming and linkage to the BAS. Essential Duties include, but are not limited to, the following: Assist in commissioning, programming, setting up graphics, communications link, end to end testing, troubleshooting and servicing on assigned projects. Document point to point verification, sequence of operations validation and job close out requirements. Represent the company by serving as the direct customer contact and is responsible for servicing products and equipment on assigned projects, ensuring customer satisfaction by identifying, diagnosing and repairing equipment and systems at customer's location. Coordinate with team leader and customer to precisely understand requirements for all on-site installation and repairs by forecasting issues, gathering materials and synchronizing on-site work. Keep current on industry products concerning installation, operation, maintenance, service, and repair of direct digital control systems. Continually enforce safety to the highest standards and maintains security and accountability of company issued and procured assets by recording use, wear and conditions. Install, maintain, operate, and repair of all Exact Sciences' BAS control systems, including preventive maintenance. Work with engineering or scientific personnel to discuss plans, modifications, and user needs. Review available plans, specifications, or mechanical, electrical, and plumbing (MEP) drawings. Perform system and subsystem diagnostics, schedule and maintain complex electronic environmental systems, and calibrate unique components and controls that are used to provide and monitor precise environmental conditions within Exact Sciences facilities. Provide expertise and technical assistance for a 24-hour operational environment with limited documentation resources. Respond to service calls and preventive maintenance inspections. Track the performance of routine and preventative maintenance to ensure availability of HVAC systems. Participate in improvement activities that improve the process, work, and make recommendations for enhancing the systems and procedures. Inspect and test systems to verify system compliance with plans and specifications or to detect and locate malfunctions. React to loss of critical utility outages, as well as assist in restoration efforts following weather-related events. Provide technical support and expertise for automated equipment, building infrastructure, systems, and controls to maintain efficient and reliable operation, including the completion of accurate and up to date good manufacturing practice (GMP) documentation. Analyze, diagnose, and repair equipment documenting work as required by the quality management system (QMS). Monitor, repair, and maintain electrical, mechanical, and plumbing systems and equipment or coordinate the services of contractors and/or the landlord. Conduct building inspections to assess the current operational condition, document findings, and take appropriate follow up action. Ensure contractor compliance with environment, health, and safety (EHS) policies and procedures, including hot work and lock out tag out. Follow standard operating procedures (SOPs). Understand the operation of commercial, medical, and industrial refrigeration systems. Maintain compliance with all regulatory standards, including GMP, Occupational Safety and Health Administration (OSHA), Food and Drug Administration (FDA), Wisconsin Department of Agriculture, Trade, and Consumer Protection (WDATCP), and United States Department of Agriculture (USDA). Participate in the on-call program for emergency service. Respond to critical alarms. Excellent oral and written communication skills. Excellent problem-solving skills. Ability to interface and work effectively with all levels of the organization, vendors, and customers. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's Quality Management System policies and procedures. Regular and reliable attendance. Ability to work a designated schedule. Ability to work overtime as needed. Ability to work nights and/or weekends. Ability to lift up to 75 pounds for approximately 5% of a typical working day. Ability to work on an electronic tape measure, mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 70% of a typical working day. Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height. Ability to comply with any applicable personal protective equipment requirements. Ability and means to travel between Madison locations. Ability to travel approximately 10% of working time away from work location, may include overnight/weekend travel. Minimum Qualifications 1+ years of experience in BAS Controls. Technical School or formal training 1+ years of experience working with facility software tools, including, but not limited to, Building Automation Systems (BAS), Computerized Maintenance Management System (CMMS), Computer-Aided Facility Management ( CAFM), and environmental monitoring. Possession of a valid driver's license, no more than two moving violations in the past 36 months, and no unresolved license revocation or suspension issues. Authorization to work in the United States without sponsorship. Demonstrated ability to perform the Essential Duties of the position with or without accommodation. Preferred Qualifications 3+ years of related experience in facilities departments in regulated environments, including laboratory, bio/pharma, industrial, and healthcare facilities. Experience in a GMP and/or ISO 13485 environment. Experience with OSHA, EPA, and FDA regulations. Experience in repair and maintenance of automated equipment. Knowledge of CLIA/CAP regulations. 10 Hour OSHA Certification. Salary Range: $51,000.00 - $84,000.00 The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible. Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits . Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here . Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law. To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub . The documents summarize important details of the law and provide key points that you have a right to know.
10/11/2025
Full time
Help us change lives At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others. Position Overview The Maintenance Technician II, BAS Controls is responsible for installing, servicing, repairing, troubleshooting and preventive maintenance on all Exact Sciences' Building Automation System (BAS) control systems. This position is responsible for a wide range of equipment from large-scale commercial-grade HVAC systems to multi-zone systems that incorporate direct digital control (DDC), pneumatic, electronic, and/or programmable logic controls. This position is responsible for installation, operation, maintenance, service, and repair of direct digital control systems and control programming and linkage to the BAS. Essential Duties include, but are not limited to, the following: Assist in commissioning, programming, setting up graphics, communications link, end to end testing, troubleshooting and servicing on assigned projects. Document point to point verification, sequence of operations validation and job close out requirements. Represent the company by serving as the direct customer contact and is responsible for servicing products and equipment on assigned projects, ensuring customer satisfaction by identifying, diagnosing and repairing equipment and systems at customer's location. Coordinate with team leader and customer to precisely understand requirements for all on-site installation and repairs by forecasting issues, gathering materials and synchronizing on-site work. Keep current on industry products concerning installation, operation, maintenance, service, and repair of direct digital control systems. Continually enforce safety to the highest standards and maintains security and accountability of company issued and procured assets by recording use, wear and conditions. Install, maintain, operate, and repair of all Exact Sciences' BAS control systems, including preventive maintenance. Work with engineering or scientific personnel to discuss plans, modifications, and user needs. Review available plans, specifications, or mechanical, electrical, and plumbing (MEP) drawings. Perform system and subsystem diagnostics, schedule and maintain complex electronic environmental systems, and calibrate unique components and controls that are used to provide and monitor precise environmental conditions within Exact Sciences facilities. Provide expertise and technical assistance for a 24-hour operational environment with limited documentation resources. Respond to service calls and preventive maintenance inspections. Track the performance of routine and preventative maintenance to ensure availability of HVAC systems. Participate in improvement activities that improve the process, work, and make recommendations for enhancing the systems and procedures. Inspect and test systems to verify system compliance with plans and specifications or to detect and locate malfunctions. React to loss of critical utility outages, as well as assist in restoration efforts following weather-related events. Provide technical support and expertise for automated equipment, building infrastructure, systems, and controls to maintain efficient and reliable operation, including the completion of accurate and up to date good manufacturing practice (GMP) documentation. Analyze, diagnose, and repair equipment documenting work as required by the quality management system (QMS). Monitor, repair, and maintain electrical, mechanical, and plumbing systems and equipment or coordinate the services of contractors and/or the landlord. Conduct building inspections to assess the current operational condition, document findings, and take appropriate follow up action. Ensure contractor compliance with environment, health, and safety (EHS) policies and procedures, including hot work and lock out tag out. Follow standard operating procedures (SOPs). Understand the operation of commercial, medical, and industrial refrigeration systems. Maintain compliance with all regulatory standards, including GMP, Occupational Safety and Health Administration (OSHA), Food and Drug Administration (FDA), Wisconsin Department of Agriculture, Trade, and Consumer Protection (WDATCP), and United States Department of Agriculture (USDA). Participate in the on-call program for emergency service. Respond to critical alarms. Excellent oral and written communication skills. Excellent problem-solving skills. Ability to interface and work effectively with all levels of the organization, vendors, and customers. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's Quality Management System policies and procedures. Regular and reliable attendance. Ability to work a designated schedule. Ability to work overtime as needed. Ability to work nights and/or weekends. Ability to lift up to 75 pounds for approximately 5% of a typical working day. Ability to work on an electronic tape measure, mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 70% of a typical working day. Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height. Ability to comply with any applicable personal protective equipment requirements. Ability and means to travel between Madison locations. Ability to travel approximately 10% of working time away from work location, may include overnight/weekend travel. Minimum Qualifications 1+ years of experience in BAS Controls. Technical School or formal training 1+ years of experience working with facility software tools, including, but not limited to, Building Automation Systems (BAS), Computerized Maintenance Management System (CMMS), Computer-Aided Facility Management ( CAFM), and environmental monitoring. Possession of a valid driver's license, no more than two moving violations in the past 36 months, and no unresolved license revocation or suspension issues. Authorization to work in the United States without sponsorship. Demonstrated ability to perform the Essential Duties of the position with or without accommodation. Preferred Qualifications 3+ years of related experience in facilities departments in regulated environments, including laboratory, bio/pharma, industrial, and healthcare facilities. Experience in a GMP and/or ISO 13485 environment. Experience with OSHA, EPA, and FDA regulations. Experience in repair and maintenance of automated equipment. Knowledge of CLIA/CAP regulations. 10 Hour OSHA Certification. Salary Range: $51,000.00 - $84,000.00 The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible. Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits . Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here . Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law. To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub . The documents summarize important details of the law and provide key points that you have a right to know.
Help us change lives At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others. Position Overview The Maintenance Technician II, BAS Controls is responsible for installing, servicing, repairing, troubleshooting and preventive maintenance on all Exact Sciences' Building Automation System (BAS) control systems. This position is responsible for a wide range of equipment from large-scale commercial-grade HVAC systems to multi-zone systems that incorporate direct digital control (DDC), pneumatic, electronic, and/or programmable logic controls. This position is responsible for installation, operation, maintenance, service, and repair of direct digital control systems and control programming and linkage to the BAS. Essential Duties include, but are not limited to, the following: Assist in commissioning, programming, setting up graphics, communications link, end to end testing, troubleshooting and servicing on assigned projects. Document point to point verification, sequence of operations validation and job close out requirements. Represent the company by serving as the direct customer contact and is responsible for servicing products and equipment on assigned projects, ensuring customer satisfaction by identifying, diagnosing and repairing equipment and systems at customer's location. Coordinate with team leader and customer to precisely understand requirements for all on-site installation and repairs by forecasting issues, gathering materials and synchronizing on-site work. Keep current on industry products concerning installation, operation, maintenance, service, and repair of direct digital control systems. Continually enforce safety to the highest standards and maintains security and accountability of company issued and procured assets by recording use, wear and conditions. Install, maintain, operate, and repair of all Exact Sciences' BAS control systems, including preventive maintenance. Work with engineering or scientific personnel to discuss plans, modifications, and user needs. Review available plans, specifications, or mechanical, electrical, and plumbing (MEP) drawings. Perform system and subsystem diagnostics, schedule and maintain complex electronic environmental systems, and calibrate unique components and controls that are used to provide and monitor precise environmental conditions within Exact Sciences facilities. Provide expertise and technical assistance for a 24-hour operational environment with limited documentation resources. Respond to service calls and preventive maintenance inspections. Track the performance of routine and preventative maintenance to ensure availability of HVAC systems. Participate in improvement activities that improve the process, work, and make recommendations for enhancing the systems and procedures. Inspect and test systems to verify system compliance with plans and specifications or to detect and locate malfunctions. React to loss of critical utility outages, as well as assist in restoration efforts following weather-related events. Provide technical support and expertise for automated equipment, building infrastructure, systems, and controls to maintain efficient and reliable operation, including the completion of accurate and up to date good manufacturing practice (GMP) documentation. Analyze, diagnose, and repair equipment documenting work as required by the quality management system (QMS). Monitor, repair, and maintain electrical, mechanical, and plumbing systems and equipment or coordinate the services of contractors and/or the landlord. Conduct building inspections to assess the current operational condition, document findings, and take appropriate follow up action. Ensure contractor compliance with environment, health, and safety (EHS) policies and procedures, including hot work and lock out tag out. Follow standard operating procedures (SOPs). Understand the operation of commercial, medical, and industrial refrigeration systems. Maintain compliance with all regulatory standards, including GMP, Occupational Safety and Health Administration (OSHA), Food and Drug Administration (FDA), Wisconsin Department of Agriculture, Trade, and Consumer Protection (WDATCP), and United States Department of Agriculture (USDA). Participate in the on-call program for emergency service. Respond to critical alarms. Excellent oral and written communication skills. Excellent problem-solving skills. Ability to interface and work effectively with all levels of the organization, vendors, and customers. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's Quality Management System policies and procedures. Regular and reliable attendance. Ability to work a designated schedule. Ability to work overtime as needed. Ability to work nights and/or weekends. Ability to lift up to 75 pounds for approximately 5% of a typical working day. Ability to work on an electronic tape measure, mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 70% of a typical working day. Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height. Ability to comply with any applicable personal protective equipment requirements. Ability and means to travel between Madison locations. Ability to travel approximately 10% of working time away from work location, may include overnight/weekend travel. Minimum Qualifications 1+ years of experience in BAS Controls. Technical School or formal training 1+ years of experience working with facility software tools, including, but not limited to, Building Automation Systems (BAS), Computerized Maintenance Management System (CMMS), Computer-Aided Facility Management ( CAFM), and environmental monitoring. Possession of a valid driver's license, no more than two moving violations in the past 36 months, and no unresolved license revocation or suspension issues. Authorization to work in the United States without sponsorship. Demonstrated ability to perform the Essential Duties of the position with or without accommodation. Preferred Qualifications 3+ years of related experience in facilities departments in regulated environments, including laboratory, bio/pharma, industrial, and healthcare facilities. Experience in a GMP and/or ISO 13485 environment. Experience with OSHA, EPA, and FDA regulations. Experience in repair and maintenance of automated equipment. Knowledge of CLIA/CAP regulations. 10 Hour OSHA Certification. Salary Range: $51,000.00 - $84,000.00 The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible. Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits . Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here . Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law. To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub . The documents summarize important details of the law and provide key points that you have a right to know.
10/01/2025
Full time
Help us change lives At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others. Position Overview The Maintenance Technician II, BAS Controls is responsible for installing, servicing, repairing, troubleshooting and preventive maintenance on all Exact Sciences' Building Automation System (BAS) control systems. This position is responsible for a wide range of equipment from large-scale commercial-grade HVAC systems to multi-zone systems that incorporate direct digital control (DDC), pneumatic, electronic, and/or programmable logic controls. This position is responsible for installation, operation, maintenance, service, and repair of direct digital control systems and control programming and linkage to the BAS. Essential Duties include, but are not limited to, the following: Assist in commissioning, programming, setting up graphics, communications link, end to end testing, troubleshooting and servicing on assigned projects. Document point to point verification, sequence of operations validation and job close out requirements. Represent the company by serving as the direct customer contact and is responsible for servicing products and equipment on assigned projects, ensuring customer satisfaction by identifying, diagnosing and repairing equipment and systems at customer's location. Coordinate with team leader and customer to precisely understand requirements for all on-site installation and repairs by forecasting issues, gathering materials and synchronizing on-site work. Keep current on industry products concerning installation, operation, maintenance, service, and repair of direct digital control systems. Continually enforce safety to the highest standards and maintains security and accountability of company issued and procured assets by recording use, wear and conditions. Install, maintain, operate, and repair of all Exact Sciences' BAS control systems, including preventive maintenance. Work with engineering or scientific personnel to discuss plans, modifications, and user needs. Review available plans, specifications, or mechanical, electrical, and plumbing (MEP) drawings. Perform system and subsystem diagnostics, schedule and maintain complex electronic environmental systems, and calibrate unique components and controls that are used to provide and monitor precise environmental conditions within Exact Sciences facilities. Provide expertise and technical assistance for a 24-hour operational environment with limited documentation resources. Respond to service calls and preventive maintenance inspections. Track the performance of routine and preventative maintenance to ensure availability of HVAC systems. Participate in improvement activities that improve the process, work, and make recommendations for enhancing the systems and procedures. Inspect and test systems to verify system compliance with plans and specifications or to detect and locate malfunctions. React to loss of critical utility outages, as well as assist in restoration efforts following weather-related events. Provide technical support and expertise for automated equipment, building infrastructure, systems, and controls to maintain efficient and reliable operation, including the completion of accurate and up to date good manufacturing practice (GMP) documentation. Analyze, diagnose, and repair equipment documenting work as required by the quality management system (QMS). Monitor, repair, and maintain electrical, mechanical, and plumbing systems and equipment or coordinate the services of contractors and/or the landlord. Conduct building inspections to assess the current operational condition, document findings, and take appropriate follow up action. Ensure contractor compliance with environment, health, and safety (EHS) policies and procedures, including hot work and lock out tag out. Follow standard operating procedures (SOPs). Understand the operation of commercial, medical, and industrial refrigeration systems. Maintain compliance with all regulatory standards, including GMP, Occupational Safety and Health Administration (OSHA), Food and Drug Administration (FDA), Wisconsin Department of Agriculture, Trade, and Consumer Protection (WDATCP), and United States Department of Agriculture (USDA). Participate in the on-call program for emergency service. Respond to critical alarms. Excellent oral and written communication skills. Excellent problem-solving skills. Ability to interface and work effectively with all levels of the organization, vendors, and customers. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's Quality Management System policies and procedures. Regular and reliable attendance. Ability to work a designated schedule. Ability to work overtime as needed. Ability to work nights and/or weekends. Ability to lift up to 75 pounds for approximately 5% of a typical working day. Ability to work on an electronic tape measure, mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 70% of a typical working day. Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height. Ability to comply with any applicable personal protective equipment requirements. Ability and means to travel between Madison locations. Ability to travel approximately 10% of working time away from work location, may include overnight/weekend travel. Minimum Qualifications 1+ years of experience in BAS Controls. Technical School or formal training 1+ years of experience working with facility software tools, including, but not limited to, Building Automation Systems (BAS), Computerized Maintenance Management System (CMMS), Computer-Aided Facility Management ( CAFM), and environmental monitoring. Possession of a valid driver's license, no more than two moving violations in the past 36 months, and no unresolved license revocation or suspension issues. Authorization to work in the United States without sponsorship. Demonstrated ability to perform the Essential Duties of the position with or without accommodation. Preferred Qualifications 3+ years of related experience in facilities departments in regulated environments, including laboratory, bio/pharma, industrial, and healthcare facilities. Experience in a GMP and/or ISO 13485 environment. Experience with OSHA, EPA, and FDA regulations. Experience in repair and maintenance of automated equipment. Knowledge of CLIA/CAP regulations. 10 Hour OSHA Certification. Salary Range: $51,000.00 - $84,000.00 The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible. Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits . Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here . Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law. To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub . The documents summarize important details of the law and provide key points that you have a right to know.
What we offer You will work on exciting and challenging topics together with a team in an ultra-modern, innovative and creative environment. Intensive on-the-job training with expert colleagues guarantees you will quickly become familiar with your duties and perform them independently. Performance related pay and the opportunity for personal and professional development are of course part of the package. Since 2009 Evonik Industries AG has been certified as a family-friendly company by the German Hertie Foundation. Click here to learn more about Evonik from our employees This position is a contributor to the safe and efficient operation of the Pasadena, TX chemical facility. This position will focus on improvement and process troubleshooting efforts to optimize production rates, yield and quality while maintaining a high level of plant safety. The Production Engineer will provide technical solutions and ideas tailored around safety mitigation, process optimization and cost management. The position will also have PM/PR responsibilities supporting Pasadena site CAPEX. This position has all of the responsibilities/knowledge as a Production Engineer II with added activities in engineering mentoring/growth and the ability to manage all levels of CAPEX projects for the site. RESPONSIBILITIES Implement improvement projects by using data from Stable Ops, OEE and First Time Prime. Develop scope for these projects, as well as, time schedules and cost estimates for all sized CAPEX, as needed. Ensure successful completion of documentation for technical changes and projects under their management, including EHS documentation. Support safety and environmental process activities Continuous improvement in productivity of the manufacturing facility. This includes working with plant personnel to improve rates and yields through changes to process equipment, procedures, and operator training. Perform failure and root cause analysis and make technical recommendations for repairs and replacements considering economics and plant availability risks Mentor less experienced FTE engineers, as well as, assist in leading the growth/development of rotational engineers Ensure compliance with all elements of process safety management including manufacturing procedures, participating in project and design hazard reviews, PHRs, MOC reviews REQUIREMENTS Minimum BS ChE with at least 7+ years of experience in chemical manufacturing Experience with batch chemical processes preferred Leading and executing capital projects within budget Utilities experience would be a plus Strong technical problem-solving ability Strong teamwork and interpersonal skills Skilled in successfully overcoming technical challenges Skilled in identifying opportunities for optimization and implementing ideas Proficiency with data historians and trending software such as ASPEN Your Application To ensure the fastest process of your application and to protect the environment, please apply online via our careers portal at . VACANCY REFERENCE NUMBER 147302 Evonik Corporation is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, gender, sexual orientation, national origin, disability status, protected veteran status or any other legally protected status. Please note that Evonik will not accept any unsolicited application documents sent by staffing firms. Evonik works in conjunction with preferred service providers and will not pay any fee to staffing firms in the absence of an appropriate framework agreement. Should Evonik receive a candidate profile from a staffing firm with which it has no framework agreement, and should this candidate subsequently be considered in the recruitment process or offered employment, no claims from the staffing firm will be entertained in this regard.
11/06/2021
Full time
What we offer You will work on exciting and challenging topics together with a team in an ultra-modern, innovative and creative environment. Intensive on-the-job training with expert colleagues guarantees you will quickly become familiar with your duties and perform them independently. Performance related pay and the opportunity for personal and professional development are of course part of the package. Since 2009 Evonik Industries AG has been certified as a family-friendly company by the German Hertie Foundation. Click here to learn more about Evonik from our employees This position is a contributor to the safe and efficient operation of the Pasadena, TX chemical facility. This position will focus on improvement and process troubleshooting efforts to optimize production rates, yield and quality while maintaining a high level of plant safety. The Production Engineer will provide technical solutions and ideas tailored around safety mitigation, process optimization and cost management. The position will also have PM/PR responsibilities supporting Pasadena site CAPEX. This position has all of the responsibilities/knowledge as a Production Engineer II with added activities in engineering mentoring/growth and the ability to manage all levels of CAPEX projects for the site. RESPONSIBILITIES Implement improvement projects by using data from Stable Ops, OEE and First Time Prime. Develop scope for these projects, as well as, time schedules and cost estimates for all sized CAPEX, as needed. Ensure successful completion of documentation for technical changes and projects under their management, including EHS documentation. Support safety and environmental process activities Continuous improvement in productivity of the manufacturing facility. This includes working with plant personnel to improve rates and yields through changes to process equipment, procedures, and operator training. Perform failure and root cause analysis and make technical recommendations for repairs and replacements considering economics and plant availability risks Mentor less experienced FTE engineers, as well as, assist in leading the growth/development of rotational engineers Ensure compliance with all elements of process safety management including manufacturing procedures, participating in project and design hazard reviews, PHRs, MOC reviews REQUIREMENTS Minimum BS ChE with at least 7+ years of experience in chemical manufacturing Experience with batch chemical processes preferred Leading and executing capital projects within budget Utilities experience would be a plus Strong technical problem-solving ability Strong teamwork and interpersonal skills Skilled in successfully overcoming technical challenges Skilled in identifying opportunities for optimization and implementing ideas Proficiency with data historians and trending software such as ASPEN Your Application To ensure the fastest process of your application and to protect the environment, please apply online via our careers portal at . VACANCY REFERENCE NUMBER 147302 Evonik Corporation is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, gender, sexual orientation, national origin, disability status, protected veteran status or any other legally protected status. Please note that Evonik will not accept any unsolicited application documents sent by staffing firms. Evonik works in conjunction with preferred service providers and will not pay any fee to staffing firms in the absence of an appropriate framework agreement. Should Evonik receive a candidate profile from a staffing firm with which it has no framework agreement, and should this candidate subsequently be considered in the recruitment process or offered employment, no claims from the staffing firm will be entertained in this regard.
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
03/07/2021
Full time
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
Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovation and growth opportunities. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect life. I. JOB SUMMARY The QC Analyst III, position supports the Quality Control group at Emergent BioSolutions Rockville Campus. The role requires knowledge and understanding of scientific concepts, practices and procedures within the biopharmaceutical field and a cGMP environment. The role is responsible for daily routine testing and laboratory maintenance tasks such as Environmental Monitoring of the GMP area, and sampling and testing of water, compressed air, nitrogen and bioburden testing samples. T Individuals should be able to work independently and participate in cross functional teams for Operation Excellence, Root Cause analysis, and risk assessments. In this role, Individuals will use soft skills, to work on QC schedules and to work with internal customers (EHS, Manufacturing and QA). People leader skills will be cultivated in this role. II. ESSENTIAL FUNCTIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Assist the Manager, QC Micro / Analytical with feasibility assessment of client projects Perform microbiological / analytical work per method transfer/ validation programs. Perform environmental monitoring and utility testing of the facility. Performs environmental monitoring during fill operations (as necessary) Write method validation / transfer protocols and reports as necessary. Perform various microbiological / analytical testing procedures per Quality Control batch records and stability protocols. Inform supervisor/manager upon observing OOS, OOL, or generation of deviations. Participate in investigations of OOS results and other related studies.Assist with complex investigations by obtaining root cause and implementing changes. Participate in calibration, troubleshooting various types of equipment including proactive resolution of instrument issues. Write, review, and revise SOP's and Testing Standards as necessary. Train additional employees in methods, transfers and techniques Review, analyze, interpret and report data. Practice Good Documentation and Laboratory Safety Procedures per the Standard Operating Procedures. Resource for technical knowledge of current assays Uses analytical and statistical concepts to understand variable sin assays Assess the compliance status of current test methods and equipment Applies analytical knowledge to support change and risk management Review record keeping and documentation of laboratory equipment maintenance. Work with Project Managers and QA to ensure timely review and approval of protocols /reports. Support department compliance and productivity goals. Participate in meetings as required. Track time worked per project. Interview and recommend the employment of technical and professional supporting staff. Identify and implement continuous improvement opportunities to reduce non-value added work or complexity. May require work on weekends and nights, travel, or work with 3rd party vendors. Detailed oriented - Able to complete required tasks and associated documentation with minimal error. Adaptability - Maintain positive attitude in a changing work environment. Communication - Effectively communicates with all levels of manufacturing and support staff. Actively participate in department level meetings. Escalates issues through the proper channels. The above statements are intended to describe the general nature of work performed by those in this job. It is not an exhaustive list of all duties, and other duties may be assigned. III. MINIMUM EDUCATION, EXPERIENCE, SKILLS Education: BS in Microbiology/Biology or related field Experience: 3-5 years (MS with 3+ years) in the Pharmaceutical or Biotechnology with emphasis in aseptic processing, QC microbiology, environmental monitoring, water system, quality control, validation and manufacturing processes. Track record of achievement and sustained performance in a cGMP/GLP environment. Strong technical and communication skills: oral/written and listening. Personal Competencies: Self - awareness, Integrity, Team Player, Creative and Flexible Skills: Knowledge of MS Word, Excel and PowerPoint. Other Requirements: R equires vaccination against different viruses including Vaccinia virus. There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate. Reasonable accommodations may be made to enable individuals with disabilities to perform all essential functions. Emergent BioSolutions is an Equal Opportunity/Affirmative Action Employer and values the diversity of our workforce. Emergent does not discriminate on the basis of race, color, creed, religion, sex or gender (including pregnancy, childbirth, and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, age, national origin, ancestry, citizenship status, marital status, physical or mental disability, military service or veteran status, genetic information or any other characteristics protected by applicable federal, state or local law. Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy . Emergent BioSolutions does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Emergent BioSolutions' approved agency list. Unsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions' approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency. .buttontextde38d a{ border: 1px solid transparent; } .buttontextde38d a:focus{ border: 1px dashed #c11d4b !important; outline: none !important; }
01/26/2021
Full time
Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovation and growth opportunities. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect life. I. JOB SUMMARY The QC Analyst III, position supports the Quality Control group at Emergent BioSolutions Rockville Campus. The role requires knowledge and understanding of scientific concepts, practices and procedures within the biopharmaceutical field and a cGMP environment. The role is responsible for daily routine testing and laboratory maintenance tasks such as Environmental Monitoring of the GMP area, and sampling and testing of water, compressed air, nitrogen and bioburden testing samples. T Individuals should be able to work independently and participate in cross functional teams for Operation Excellence, Root Cause analysis, and risk assessments. In this role, Individuals will use soft skills, to work on QC schedules and to work with internal customers (EHS, Manufacturing and QA). People leader skills will be cultivated in this role. II. ESSENTIAL FUNCTIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Assist the Manager, QC Micro / Analytical with feasibility assessment of client projects Perform microbiological / analytical work per method transfer/ validation programs. Perform environmental monitoring and utility testing of the facility. Performs environmental monitoring during fill operations (as necessary) Write method validation / transfer protocols and reports as necessary. Perform various microbiological / analytical testing procedures per Quality Control batch records and stability protocols. Inform supervisor/manager upon observing OOS, OOL, or generation of deviations. Participate in investigations of OOS results and other related studies.Assist with complex investigations by obtaining root cause and implementing changes. Participate in calibration, troubleshooting various types of equipment including proactive resolution of instrument issues. Write, review, and revise SOP's and Testing Standards as necessary. Train additional employees in methods, transfers and techniques Review, analyze, interpret and report data. Practice Good Documentation and Laboratory Safety Procedures per the Standard Operating Procedures. Resource for technical knowledge of current assays Uses analytical and statistical concepts to understand variable sin assays Assess the compliance status of current test methods and equipment Applies analytical knowledge to support change and risk management Review record keeping and documentation of laboratory equipment maintenance. Work with Project Managers and QA to ensure timely review and approval of protocols /reports. Support department compliance and productivity goals. Participate in meetings as required. Track time worked per project. Interview and recommend the employment of technical and professional supporting staff. Identify and implement continuous improvement opportunities to reduce non-value added work or complexity. May require work on weekends and nights, travel, or work with 3rd party vendors. Detailed oriented - Able to complete required tasks and associated documentation with minimal error. Adaptability - Maintain positive attitude in a changing work environment. Communication - Effectively communicates with all levels of manufacturing and support staff. Actively participate in department level meetings. Escalates issues through the proper channels. The above statements are intended to describe the general nature of work performed by those in this job. It is not an exhaustive list of all duties, and other duties may be assigned. III. MINIMUM EDUCATION, EXPERIENCE, SKILLS Education: BS in Microbiology/Biology or related field Experience: 3-5 years (MS with 3+ years) in the Pharmaceutical or Biotechnology with emphasis in aseptic processing, QC microbiology, environmental monitoring, water system, quality control, validation and manufacturing processes. Track record of achievement and sustained performance in a cGMP/GLP environment. Strong technical and communication skills: oral/written and listening. Personal Competencies: Self - awareness, Integrity, Team Player, Creative and Flexible Skills: Knowledge of MS Word, Excel and PowerPoint. Other Requirements: R equires vaccination against different viruses including Vaccinia virus. There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate. Reasonable accommodations may be made to enable individuals with disabilities to perform all essential functions. Emergent BioSolutions is an Equal Opportunity/Affirmative Action Employer and values the diversity of our workforce. Emergent does not discriminate on the basis of race, color, creed, religion, sex or gender (including pregnancy, childbirth, and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, age, national origin, ancestry, citizenship status, marital status, physical or mental disability, military service or veteran status, genetic information or any other characteristics protected by applicable federal, state or local law. Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy . Emergent BioSolutions does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Emergent BioSolutions' approved agency list. Unsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions' approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency. .buttontextde38d a{ border: 1px solid transparent; } .buttontextde38d a:focus{ border: 1px dashed #c11d4b !important; outline: none !important; }
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 Upstream and Downstream Senior Associate will perform daily cGMP manufacturing for plasmid products including upstream, purification, media/buffer production, and general suite/operational readiness activities. The manufacturing associate is responsible for providing direction for the Manufacturing Associates I-III, with the Supervisor's oversight. 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 Prepare for production by reviewing production schedule; studying and clarifying specifications; calculating requirements; assembling materials and supplies Provide written and verbal updates to supervisors or other department managers 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 B.S. in Biology, or related field preferred. 3+ years Manufacturing experience with demonstrated progression from Associate I-III 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 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. 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 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. No travel required. Communicate using telephone and e-mail BENEFITS Arranta Bio is an Equal Opportunity Employer.
01/19/2021
Full time
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 Upstream and Downstream Senior Associate will perform daily cGMP manufacturing for plasmid products including upstream, purification, media/buffer production, and general suite/operational readiness activities. The manufacturing associate is responsible for providing direction for the Manufacturing Associates I-III, with the Supervisor's oversight. 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 Prepare for production by reviewing production schedule; studying and clarifying specifications; calculating requirements; assembling materials and supplies Provide written and verbal updates to supervisors or other department managers 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 B.S. in Biology, or related field preferred. 3+ years Manufacturing experience with demonstrated progression from Associate I-III 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 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. 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 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. No travel required. 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 Cell Banking Sr. Manufacturing Associate will perform 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 Sr. Manufacturing Associate is responsible for providing direction for the Manufacturing Associates I-III, with the Supervisor's oversight. ESSENTIAL JOB FUNCTIONS Perform cell banking and final fill activities utilizing aseptic technique while working within a biological safety cabinet in a commercial cGMP environment Preparation of media and buffers Prepare for production by reviewing production schedule; studying and clarifying specifications; calculating requirements; assembling materials and supplies Provide written and verbal updates to supervisors or other department managers 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. 3+ years Manufacturing experience with demonstrated progression from Associate I-III Master Cell Bank production and Final Fill Experience 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 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. 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 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. Communicate using telephone and e-mail.
01/17/2021
Full time
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 Cell Banking Sr. Manufacturing Associate will perform 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 Sr. Manufacturing Associate is responsible for providing direction for the Manufacturing Associates I-III, with the Supervisor's oversight. ESSENTIAL JOB FUNCTIONS Perform cell banking and final fill activities utilizing aseptic technique while working within a biological safety cabinet in a commercial cGMP environment Preparation of media and buffers Prepare for production by reviewing production schedule; studying and clarifying specifications; calculating requirements; assembling materials and supplies Provide written and verbal updates to supervisors or other department managers 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. 3+ years Manufacturing experience with demonstrated progression from Associate I-III Master Cell Bank production and Final Fill Experience 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 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. 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 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. Communicate using telephone and e-mail.
