13 jobs found

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients- that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Your Role Are you ready to take your engineering career to the next level? Look no further! Vantive is seeking a highly skilled Principal Engineer, Materials Scientist to join our exceptional Disposables R&D team in Plymouth. As a world-class leader in healthcare, Vantive is dedicated to improving the lives of millions of patients worldwide. This is a unique opportunity to be part of our ambitious mission and make a real impact. The Principal Engineer, Materials Scientist will apply specialized knowledge of materials and material processing to achieve a technical vision for research and design of containers and disposable products used in multiple Kidney care modalities. You will p rovide leadership to design and manufacturing teams directing extrusion, molding, material processing and design transfer. What you will be doing: Develop products/processes (materials, design, quality improvement, research techniques) incorporating multiple tasks in the disciplines of materials science and engineering for Renal products. Serve as the technical materials expert for design change programs ( new products, suppliers, materials, labeling, CAPA/NCR, cost reduction, remediation ). Produce pilot production runs of materials and sheeting for the use in the development process and to establish process capability. Study design and hands on support with polymeric materials characterization , blending and processing Identify , investigate, and solve complex engineering problems utilizing risk-based and customer focused approaches and engineering tools. ( e.g. dFMEA , Human Factors Engineering, statistical software, CAD). Coordinate and communicate the efforts of R&D in collaboration with g lobal cross-functional stakeholders. Schedule, budget, and lead engineering projects with minimal guidance. Adhere to design control procedures, general safety rules, company policies and procedures, FDA and international regulations and guidance . May supervise engine ers and/or technicians. May c ontribute to Vantive intellectual property through invention disclosures and patent applications. What you will bring: BS in Material Science or Engineering, Chemistry, Chemical Engineering or related science or engineering field . MS or PhD preferred. 10 + years of related experience in disposables medical product development. Advanced knowledge of chemistry, material science and general engineering principles related to the development of new plastic materials Advanced knowledge of plastic material processing including injection molding, extrusion, ultrasonic welding, UV/solvent bonding, and sterilization . K nowledge of FDA Design Controls and ISO 13485 Quality Management Systems desired. K nowledge of ANSI/AAMI/ISO 14971 Medical Devices - Application o f Risk Management t o Medical Devices desired Takes initiative with a high aptitude for learning, innovation, and implementing best practices and continuous improvements . Schedule, budget, and lead engineering projects with minimal guidance. Ability to train and coach others in area of technical expertise . S elf-directed, resourceful, and able to manage multiple priorities. Strong interpersonal, communication, collaboration and influencing skills. Vantive is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. We understand compensation is an important factor as you consider the next step in your career. At Vantive, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $104,000-130,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. US Benefits at Vantive This is where your well-being matters. Vantive offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical, dental and vision coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Aon Pooled Employer Plan ("Aon PEP"), Vantive's 401(k) retirement savings plan, to help you prepare for your future. The Aon PEP is designed to help improve retirement outcomes by providing retirement resources more efficiently. The plan offers a robust set of investment options, financial education, and a suite of resources to support your retirement goals. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Vantive's US Benefits, please speak with your recruiter or visit our Benefits site: Benefits Vantive Equal Employment Opportunity Vantive is an equal opportunity employer. Vantive evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice .

About Us SharkNinja is a global product design and technology company, with a diversified portfolio of 5-star rated lifestyle solutions that positively impact people's lives in homes around the world. Powered by two trusted, global brands, Shark and Ninja , the company has a proven track record of bringing disruptive innovation to market, and developing one consumer product after another has allowed SharkNinja to enter multiple product categories, driving significant growth and market share gains. Headquartered in Needham, Massachusetts with more than 3,600+ associates, the company's products are sold at key retailers, online and offline, and through distributors around the world . At SharkNinja, we are redefining how products improve everyday life-and our Senior Director of Design & Advanced Development sits at the very heart of that ambition. We're seeking a creative leader and future thinker to head up our global Front-End Innovation team: a passionate, hands-on group of design storytellers, engineers, and inventors who bring breakthrough product ideas to life. This isn't just a design leadership role-it's about leading the spark behind SharkNinja's next generation of iconic products. You'll be the creative catalyst shaping what's next, helping teams turn blue-sky thinking into tangible, consumer-loved innovations that define categories. Your team will shape the early concept architecture that eventually fuels mass production through our NPD (New Product Development) pipeline. The ideal candidate is a designer at heart, with deep engineering and design credentials, a natural flair for storytelling, and a relentless passion for solving consumer problems in inventive, inspiring ways. What You'll Do Lead SharkNinja's Front-End Innovation team, responsible for driving concept creation, design storytelling, and early platform exploration across all product categories. Inspire a team of Industrial Designers and Product Design Engineers to generate physical and visual prototypes that sell ideas and excite cross-functional partners and senior executives. Be a design storyteller-capable of pitching future-focused concepts in a way that connects emotionally and drives alignment across the business. Champion a studio culture that blends hands-on making, iterative sketching, advanced prototyping, and bold thinking grounded in technical feasibility. Partner with Mechanical Engineering, R&D, Product Development, and Product Marketing to ensure early concepts are rooted in a strong, scalable product strategy. Integrate deep knowledge of materials, manufacturing methods (e.g., plastic injection molding, die casting, sheet metal), and DFM/DFA to ensure ideas are not just exciting-but achievable. Bring context and imagination to every phase of development, combining user insights, trend forecasting, and emerging technologies to shape future design visions. Cultivate a high-energy environment where curiosity, creativity, and invention are celebrated and continuously pushed forward. Maintain a consumer-obsessed mindset, with a focus on developing products that change behaviors, exceed expectations, and lead markets. What You'll Bring A degree in Product Design Engineering, Industrial Design, or a related field that blends design and engineering. A PDE background is highly valued for its unique balance of technical rigor and creative thinking. 10+ years of experience in product design and innovation, ideally in high-volume consumer goods environments. A rich portfolio of category-defining consumer products that demonstrate design excellence, storytelling, and successful commercialization. Proven leadership in building and developing creative teams-mentoring talent, championing new voices, and fostering collaboration across disciplines. An ability to lead with vision and conviction while remaining hands-on, detail-oriented, and deeply engaged in the creative process. A natural presenter and communicator, with the charisma and clarity to sell ideas across all levels of the organization-from engineers to executives. Strong technical foundation in high-volume manufacturing and an appreciation for the intersection of creativity and feasibility. A love for "making"-whether sketching, building, modeling, or hacking together ideas to inspire others. Bold thinking, grounded in insight, empathy, and a deep understanding of consumer behavior. A proficiency in SolidWorks or Creo, KeyShot, and Adobe Suite. Why This Role Matters This role is more than just product design-it's about shaping our future. You will lead a team of makers, storytellers, and engineers to uncover what's next, spark new possibilities, and turn compelling ideas into category-changing products. If you're obsessed with invention, fueled by creativity, and ready to lead a team that lives at the edge of what's possible-this is your moment. Salary and Other Compensation: The annual salary range for this position is displayed below. Factors which may affect starting pay within this range may include geography/market, skills, education, experience and other qualifications of the successful candidate. Pay Range $264,510 $323,290 USD Our Culture At SharkNinja, we don't just raise the bar-we push past it every single day. Our Outrageously Extraordinary mindset drives us to tackle the impossible, push boundaries, and deliver results that others only dream of. If you thrive on breaking out of your swim lane, you'll be right at home. What We Offer We offer competitive health insurance, retirement plans, paid time off, employee stock purchase options, wellness programs, SharkNinja product discounts, and more. We empower your personal and professional growth with high impact Learning Programs featuring bold voices redefining what's possible. When you join, you're not just part of a company-you're part of an outrageously extraordinary community. To gether, we won't just launch products- we'll disrupt entire markets. At SharkNinja, Diversity, Equity, and Inclusion are vital to our global success. Valuing each unique voice and blending all of our diverse skills strengthens SharkNinja's innovation every day. We support ALL associates in bringing their authentic selves to work, making an impact, and having the opportunity for career acceleration. With help from our leadership, associates, and our community, we aim to have equity be a key component of the SharkNinja DNA. Learn more about us: Life At SharkNinja Outrageously Extraordinary SharkNinja Candidate Privacy Notice For candidates based in all regions, please refer to this Candidate Privacy Notice . For candidates based in China, please refer to this Candidate Privacy Notice . For candidates based in Vietnam, please refer to this Candidate Privacy Notice . We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, disability, or any other class protected by legislation, and local law. SharkNinja will consider reasonable accommodations consistent with legislation, and local law. If you require a reasonable accommodation to participate in the job application or interview process, please contact SharkNinja People & Culture at

Description: Position: Plastics Engineer Location: Hudson, MA (on-site) Schedule: Monday to Friday 8am to 5pm Compensation: Negotiable based on experience/fair market value Employment Type: Full-Time, Direct Hire Benefits offered to you: Paid Time Off including holidays and vacation Health, Dental, and Vision insurance 2 Health Plan Options One with fully reimbursed deductible! Flexible Spending Account Dependent Care Reimbursement Account 401(k) with company match Company provided group life insurance and AD&D Company provided short-term disability coverage Optional long-term disability coverage Optional Cancer Insurance and Extended Illness Insurance Employee Referral Bonuses Purpose & Scope: This role will be responsible for evaluating new and current tools to enhance manufacturability, manage project development from conceptualization through production, and assist with the pricing and quoting of customer projects to ensure competitive yet profitable project deliverables. Essential Duties May Include: Managing custom customer projects and serving as their key point of contact Receiving and processing orders, verifying terms are agreeable with quotes, and ensuring all documents are completed Reviewing customer data files and/or blueprints for the purpose of submitting a bid or proposal to potential customers for tooling costs, plastic piece prices, and secondary operations Producing reliable estimates of costs to manufacture products and verifying the tooling provided by suppliers meets all requirements for efficient production Reviewing and approving all tool designs and design changes. Maintaining appropriate documentation files for all products, tooling, and related information Expediting orders, following up on behalf of the customer, and apprising the customer of order status Ensuring complete and accurate filing of customer history folders, pricing data, and related records/reports Partnering with manufacturing team to verify projects are set-up for production and all tooling is working effectively Requirements: The ideal candidate will have : 8+ years of prior experience in custom injection molding Bachelors degree or higher in Plastics Engineering or a related discipline Knowledge of mold building, raw materials, equipment, and molding techniques Prior use of IQMS, SolidWorks/AutoCAD PI421c0ccbd13c-8401

With over 70 years of innovative products and services, Valto is the world's leading provider of FRP composite panels. Our lightweight composite products deliver unsurpassed strength and durability; and we continue to pioneer next level performance in building materials, recreational vehicles, and transportation. We deliver quality products that perform in demanding environments. Valto is searching for a R&D Material Scientist to be based out of our Bolingbrook, IL facility. Reporting to the Research and Development Manager, this role focuses on the development and commercialization of innovative composite materials and processes that drive profitable growth across multiple business segments. You'll collaborate closely with internal teams and external partners-including suppliers and customers-to bring cutting-edge solutions to market. The ideal candidate will have 8 years of experience with materials development specifically in composites, resin formulation, or other polymer applications. Demonstrated experience in project leadership highly preferred. How you'll make an impact: Drive and independently lead projects associated with thermoset composites, including new product development, study of material interactions, and fundamental resin chemistry. Work closely with each market segment to ensure alignment with strategic goals. Lead and support process changes, raw material changes, and quality issues related to existing and new products across multiple manufacturing locations. Complete technical reports with analysis and findings. Analyze experimental data, summarize key findings, and report out in team settings. Work with the sales team to leverage technical findings and product properties for share gains. Establish relationships with customers to capture VOC and product application insight Stay current in latest technology in the composites industry and seek out new materials, ideas, and concepts to develop differentiated, innovative prototypes with potential for scale-up. Work on advanced, complex technical projects or business issues requiring state-of-the-art technical or industry knowledge. What you bring to the table: BS in Materials Science, Chemistry, Engineering or other suitable technical field required, advanced degree preferred. Extensive hands-on experience with mechanical testing and physical and chemical properties of materials. Experience with composites manufacturing preferred, including but not limited to: open molding and close molding, pultrusion, extrusion, injection molding, compression molding Formulation and compounding with a wide variety of materials, including but not limited to: thermoset resins, thermoplastics, fibers, films and coatings, nanocomposites, composites additives, "Green" materials and processes including recycling Process development experience, including small scale to large commercial scale. Experience with Matlab, Minitab, Python, R, or other programming tools Development of intellectual property Desirable technical skills other than strong polymer chemistry skills include: analytical instrumentation, statistics, design of experiment, mathematical modeling methods, finite element analysis Salary Range $80,000 - $120,000 Valto, Inc provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws Compensation details: 00 Yearly Salary PI659bcb932e24-9489

Overview We are looking for Category Manager to join our team! Responsibilities The Category Manager for Direct Procurement is ultimately responsible for developing and deploying an all-inclusive sourcing strategy for the full scope of supply while ensuring Operational Procurement excellence and continuity of supply for approximately $ 100M in spend on Direct Non-Raw Material goods such as Plastic Fittings (Blow, Injection and Roto Molded), PVC and PVC Parts, Metal Castings, Rubber and Rubber Gaskets, and Fabricated Metal Parts . This position relies on strong leadership and drive towards results, a high degree of internal and external cross-functional collaboration and relationship management, good organizational and communication skills, and the ability to lead the execution of strategic sourcing processes that enable the achievement of business objectives. Must be customer service oriented and a solid team player. Specifically, this role will be responsible for: Develop and deploy a 3-year Strategy for the Direct Procurement Category aligned with the Business objectives. Generate Cost Savings YOY for the duration of the assignment, reporting monthly to executive team. Lead Sourcing Events, inclusive of but not limited to Online Reverse Auctions, collaborating with stakeholders to define scope, sources of supply and overall sourcing strategy. Leverage and consolidate spend, rationalizing the Supplier Base. Maximize extending Supplier payment terms for FCF optimization. Implement effective and comprehensive Supplier Relationship Management programs. Lead strategic Procurement initiatives such as Industry and Market Analysis & Benchmarking, Risk Mitigation Plans, Supplier Performance Improvement Plans, etc. Drive all key strategic Procurement initiatives for the Category. Leverage ADS's systems and technologies; identify opportunities for value creation through synergies of people, processes and technology. Lead commercial agreement negotiations with suppliers and ensure continuity of supply, improve lead-times, control pricing, and mitigate risk. Lead cross-functional initiatives for development of TCO and Should-Cost models, VA/ VE, Process Improvement, Trystorming, etc. Leverage and manage industry associations on behalf of ADS. Develop collaborative relationships with other ADS sourcing managers and cross functional counterparts in Supply Chain, R&D, Finance, Legal, Marketing, BT, HR, etc. Ensure organizational alignment with sourcing strategies. Leverage relationship with category business leaders to develop an in-depth understanding of ADS current and future business needs. Stay current on new laws/policies that impact ADS' compliance record relative to sourcing and supply contracts. Ensure contract disputes and supplier performance issues are resolved in a timely manner. Analyze markets and create accurate cost forecasts. Identify and exploit emerging technologies and trends. Year one critical success factors: Quickly integrate into ADS and develop strong relationships with key company stakeholders and with the supply chain team worldwide. Integrate into and own key supplier relationships. Following the initial capability assessment, design and obtain alignment to a multi-year strategy and tactics to ensure the biggest operational impact and resources/changes required for effective execution. Deliver significant Cost Savings. Professional Experience / Qualifications: The ideal candidate will be a proven procurement and business leader with experience in a public company, indirect procurement, and in a large decentralized, multi-site manufacturing organization. The candidate also must have the following experience and competencies: Knowledge of the polyvinyl chloride (PVC) market, both virgin and compounding. Knowledge of applications: injection and blow molding; rotomolding; thermomolding; gasket extrusion. Sound experience with effective end-to-end business planning processes globally. To include demand planning, supply planning, sales, inventory & operational planning (SIOP), and material requirements planning. Demonstrated capability of developing sourcing strategies for sub-commodity categories within Direct Non-Raw Material goods and related services. Track record of delivering significant bottom line impact through deployment of sourcing strategies supporting Margin Expansion, W/C Improvement and Topline Growth. Proven ability in successfully executing Strategic Sourcing Processes. Experience in developing and maintaining supply agreements and contracts. Demonstrated strong Change Management and Organizational Transformation skills. Mastery of Procurement tools and Negotiation skills, including on-the-job buying experience. Development and utilization of metrics, KPIs, scorecards and dashboard concepts. Ability to work on extremely complex problems where analysis of situations or data requires an evaluation of intangible variance factors. Excellent planning and organizational, project management, and time management skills. Strong interpersonal, verbal, and written communication skills that engage and inspire the team. Strong ability to lead in a cross-functional / matrix management environment. Demonstrated ability to transform an organization's culture through change management, development of new processes and improvement of existing ones, and to drive outstanding team performance via goal setting and prioritization, substantiated by metrics and KPIs. Experience working with both large and small teams within a matrix reporting environment. Proven ability to work on extremely complex problems where analysis of situations or data requires an evaluation of intangible variance factors. Seasoned judgment to address and resolve critical issues and make timely, complex decisions. Decision Quality: makes well-informed, collaborative, and effective decisions quickly, if necessary, based upon a mixture of analysis, wisdom, experience, and judgment; a high percentage of his/her solutions and suggestions turn out to be correct and accurate when judged over time; sought out by others for advice and solutions. Willing and able to make tough calls and unpopular decisions that are in the best interests of the business. Empowers Employees: makes sure that employees have the direction, tools, and freedom to achieve excellent results in each of their jobs; removes obstacles and focuses people on opportunities, not hurdles. Able to get people to work cross-functionally and delegates authority appropriately. Business financial assessment and related business case development. Other Critical Competencies: Safety Awareness and Conduct: must keep Safety as a number 1 priority for the organization and behaving accordingly at all times. Ability and commitment to guide, motivate, mentor and develop staff members and successors to key positions within the department. Drive Innovation - has redefined operations to support growth through analysis and novel ideas and is experienced with managing and institutionalizing innovation and purchasing practices. Demonstrated ability to enable results across functions, cultures and hierarchy. Strong leadership, communication and influencing skills to drive results in a highly decentralized organization and impact at all levels of the organization. Humble, pragmatic, ego-in-check but high levels of self-confidence in own capabilities. An inspirational leader and team player who fosters a collaborative environment and develops a strong culture enabling high levels of morale and engagement, resulting in exemplary performance in efficiency and productivity. A strategic thinker with vision combined with willingness and ability to 'roll up his/her sleeves' - able to make it happen in a fast-moving environment. Ability to identify what matters most and prioritize as well as focus efforts of team appropriately. Expert problem solver who uses data to drive informed decision making. Experience with LEAN practices and concepts. Required Personal Attributes: Working Through Ambiguity Builds Effective Teams Collaboration Influencing Skills Effective Communication Passion and Energy Results Oriented Conflict Management Education: The successful candidate will have an undergraduate degree; preferably in Business, Supply Chain Management, related Operations discipline, or Engineering. An MBA or advanced degree is preferred. PI

PROCESS ENGINEER - PLASTICS LOCATION: Lake Zurich, IL COMPENSATION: Commensurate with experience. ABOUT THE COMPANY: * Dynamic design and manufacturing company with headquarters in the Greater Chicago, IL area. * Expertise in metals and plastics serving the Automotive Industry. * Global company with a presence in the USA, Canada, Mexico and China. * Environment that is constantly growing and improving throughout their 50 year history. JOB DESCRIPTION SUMMARY: The Process Engineer will be responsible for development and documentation of process parameters for new and existing molds. Creates process parameters, specifications, establishes manufacturing control plans to improve quality. DUTIES AND RESPONSIBILITIES: * This individual will interface directly with R&D, Manufacturing and external vendors to resolve manufacturing issues in process, machine, and/or tooling. * Develop optimum processes for new and existing molds * Recommends/implement improvements to molds and equipment * Provides processing expertise and guidance to Supervisors * Mandates a working and functional knowledge of the plastic injection molding process, tooling, equipment and materials. * Facilitate engineering support for injection molding. * Suggest part design and/or tool modifications to improve part performance and moldability. * Review, critique and approve mold designs by vendors. * Launches new molds, equipment and manufacturing lines. * Perform tool and process capability studies. * Trains molding and set-up personnel. * Review tooling condition and develop appropriate expense and capital budget. * Research and develop new manufacturing processes. * Analyze manufacturing data and suggest/implement improvements. * Analyze production and machinery line. * Interact with customers, suppliers, and internal resources. * Establish the parameters for an optimal molding environment. * Analyze quality control and correct flaws. * Work with other team members and vendors. * Create validation process documentations, including water and schematic drawings * Oversees and assesses existing processes and workflows. * Provides thorough instructions for successful implementation of process changes. * Conducts risk assessments. * Contributes to departmental efforts by accomplishing related tasks as needed * Ability to set, start and sample new tooling * Participation and utilization in the companys commitment to continuous improvement. * Follow ISO/IATF, safety, and environmental procedures as well as department and corporate policies and procedures. JOB KNOWLEDGE; SKILLS AND ABILITIES: * Excellent analytical and math skills * Strong written and verbal communication skills * Ability to persuade others to change existing practices * Strong attention to detail * Proven ability to identify, assess and solve problems * Proficient with computer and information technology * Knowledge of process engineering EDUCATION AND TRAINING: * Previous experience in process engineering * Previous experience working with CAD and AutoCAD * 5 years of progressive injection molding or engineering experience. * CAD and Solid works experience and Six Sigma experience are a plus but not required. * Paulson Training * De-coupled molding training RJG TOOLS AND EQUIPMENT: * Computer and other general office equipment. * Steel toed shoes, safety glasses and ear plugs where required. Keywords: Plastic Injection Molding, AutoCAD, SolidWorks, Six Sigma, Continuous Improvement, Process Engineer, RJG Training _(The duties listed above are intended only as illustrations of the various types of work that may be performed. Other duties may be assigned are not limited to the following listed above)_ HOW TO EXPRESS INTEREST - CLICK THE APPLY BUTTON AND FOLLOW THE ONLINE INSTRUCTIONS.

Sr Mechanical Engineer- Device Engineering Amgen is currently seeking a Senior Mechanical Engineer in our Device Engineering group to support technical teams in the successful design, development, testing, and transfer of drug delivery devices. The Senior Mechanical Engineer is an experienced mechanical design engineer possessing a broad knowledge set and expertise in complex, multi-disciplinary, cross-functional product design and development efforts. In support of Amgen's mission to serve patients, the Device Engineering group at Amgen is a diverse team working to identify, develop, commercialize and continuously improve drug delivery devices in order to optimize the patient experience. The Senior Engineer will interact with global and cross-functional members from systems engineering, process engineering, device development, packaging, primary containers, device quality, and other groups. Responsibilities of this position include development, testing, transfer, and life cycle management of multiple autoinjector device commercialization efforts. Test activities will include Engineering, Characterization and GMP Verification testing and will require a strong proficiency in developing test protocols, executing hands on testing, and reporting of results to senior leadership. This role will interface with customers and vendors to facilitate the proper planning and execution of design activities including CAD design, Testing, Tool/Fixture design and Methods development. The person selected for this position will work closely with project team members to ensure that best practices are used in the execution of mechanical designs and in development of detailed engineering specifications. The person will perform device design and development, testing, analysis, modeling and design verification activities. The successful candidate may also participate in design transfer activities, test method development, and design control activities. Basic Qualifications Doctorate degree and 2 years of Engineering experience OR Master's degree and 6 years of Engineering experience OR Bachelor's degree and 8 years of Engineering experience OR Associate degree and 10 years of Engineering experience OR High School diploma / GED and 12 years of Engineering experience Responsibilities: Provide complex mechanical design support to the mechanical engineering design organization Technical documentation (Test Plans/Protocols/Reports, Engineering Assessments, Design outputs, test-lab equipment/process/control) Prepare and provide communications to leadership in support of recommendations and assessments Verification testing strategy to include the differentiation between Platform and Combination Product testing to ensure minimum duplication and maximum efficiency when executing against additional programs Ensure tests methods and test protocols are developed in a sound and robust framework with high focus on eliminating test errors Execute hands on testing of autoinjector devices, including the safe operation of test equipment Collaborate with and support manufacturing sites on design/fabrication of assembly and labeling equipment Perform solid modeling (SolidWorks) and create drawings using best practices in accordance with ANSI/ASME Y14.5 Geometric Dimensioning and Tolerancing Standard and Y14.100 Engineering Drawing Practices Contribute to and/or lead execution of drug delivery design projects in different therapeutic areas, including nephrology, oncology, psoriasis, RA Develop, execute, and review mechanical specifications, development plans, characterization plans, and other related development documents for assigned projects Assess product requirements to determine coverage of mechanical design Provide technical assistance for mechanical problems to programs as needed Evaluate alternative design concepts and perform trade-off analyses Perform technical analyses and develop design solutions that will meet reliability targets and reliability allocations to components Tolerance and robustness analysis of complex mechanical designs Create and maintain design control documents Develop and execute verification plans and procedures Design with emphasis on DFM/DFA; with close collaboration and input from manufacturing team and other engineering groups Preferred Qualifications Master's Degree in Engineering, preferred Mechanical, Electrical, or BioMed 6 or more years of progressive experience as an engineer within the medical device design field 3 or more years of experience in project leadership within a development or research, manufacturing environment, working with Medical Devices, ideally Class II and Class III Broad set of knowledge and expertise in leading complex, multi-disciplinary and cross-functional product development efforts Experience in drug/device combination product design and development Background in development, commercialization, and lifecycle management of medical devices Solid experience in documentation authoring from project start to end Experience with material & test specs generation, protocol & report writing, process & test development, prototyping, design verification, DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA Experience executing lab tests, including safe and proper operation of lab equipment (Instron tensile tester, Keyence inspection equipment, etc.) Experience conceptualizing, designing and building test fixtures Demonstrated broad exposure to HW/SW/Systems design and technical depth in one or more engineering disciplines (Electrical, Mechanical, Software, etc.) Experience in injection molded plastic part design, molding process, 3D solid modeling and device assembly Proficiency in FEA and SolidWorks 3D solid modeling of parts, large assemblies and advanced surface design Technical understanding of drawings including tolerance stacks and robustness analysis Proficiency with SAP PLM with SolidWorks integration for enterprise Experience in leading projects from development approval process. - Product design/development (design control) from concept to post product launch for Europe (EMEA/CE Mark) & US (FDA/PMA/510k) submissions Leadership ability for Characterization, Verification and Validation testing of System and Subsystem Level Performance and Reliability characteristics Deep knowledge of Quality Management System, Quality Management Policy and applicable laws and regulations as they apply to this job type/position Familiar with the following standards: US Good Manufacturing Practices (21CFR820), Quality Management (ISO 13485), Risk Management (ISO 14971), EU Medical Device requirements (Council Directive 93/42/EEC), and Medical Electrical Equipment (EN 60601) Strong background in documenting requirements and providing traceability documentation for FDA Approval - DOORS, Requisite Pro, or other similar requirements management software Knowledge of dFMEA/pFMEA Practical experience in configuration management and change control process/requirements - CCB (change control board), CIT (change implementation team) concepts Demonstrated Design for Six Sigma competency Strong communication and interpersonal skills Strong problem solving, risk assessment, and risk management skills Capable of working on multiple projects in a deadline driven environment Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin..... click apply for full job details

Description Job Description: Job Description The Mission Solutions Group at Leidos has a government contract with a classified customer in the National Capital Region that requires a Plastics & Additive Manufacturing Expert. The candidate must have experience with Selective Laser Sintering (SLS), Fused Deposition Modeling (FDM), injection molding and autoclave processing. Primary Responsibilities Lead the Additive Manufacturing contract team in all aspects of the business. Lead work with additive manufacturing and plastics manufacturing tools and equipment such as Selective Laser Sintering (SLS), Fused Deposition Modeling (FDM), injection molding, autoclaves, mold making tools and surface finishing capabilities. Assess skills, train and mentor customer staff in the proper use of Additive Manufacturing (AM) and Rapid Prototyping (RP) equipment. Provide written analysis of customer staff skills to ensure all officers can safely operate equipment. Effectively aid officers in project design and the troubleshooting of equipment and processes pertaining to 3D Printing, injection molding, sculpting, mold making and surface finishing. Maintain and document all equipment use processes and ensure all staff know where to find the documentation. Develop white papers as necessary to recommend new Plastics and Additive Manufacturing capabilities. Communicate with vendors regarding new capabilities and regarding maintenance requirements for existing machines. Maintain a thorough understanding of additive manufacturing and plastics manufacturing equipment and practices such as 3D Printing, injection molding, sculpting, mold making and surface finishing. Attain and maintain customer-specified certification with the safe handling, application, processing and disposal of Hazardous Materials. Process the receipt and disposal of HAZMAT and HAZWASTE according to EPA regulations. Develop and maintain an inventory management system. Demonstrate experience with the management of 1000+ shop supplies in a semi-automated fashion. Coordinate and communicate with all local and field personnel requiring shop support. Research equipment anomalies and recommend solutions. Provide feedback to customer staff regarding the viability of proposed future shop plans. Basic Qualifications Bachelor's degree and 8 years of relevant experience. Work experience can be used in lieu/combined with education 3 years of experience with additive manufacturing disciplines. 3 years of experience with injection molding equipment operation and maintenance. Demonstrated experience with Selective Laser Sintering (SLS) equipment operation and maintenance. Demonstrated experience with Fused Deposition Modeling (FDM) equipment operation and maintenance. Demonstrated experience with autoclave equipment operation and maintenance. Demonstrated experience leading teams, including strong customer service and interpersonal skills. Demonstrated ability to manage and prioritize multiple tasks and adapt quickly to changing requirements. Possess TS/SCI with polygraph security clearance Preferred Qualifications 3 years of experience with 3D printing. External Referral Bonus: Ineligible Potential for Telework: No Clearance Level Required: Top Secret/SCI with Polygraph Travel: Yes, 10% of the time Scheduled Weekly Hours: 40 Shift: Day Requisition Category: Professional Job Family: Manufacturing Leidos is a Fortune 500 ® information technology, engineering, and science solutions and services leader working to solve the world's toughest challenges in the defense, intelligence, homeland security, civil, and health markets. The company's 38,000 employees support vital missions for government and commercial customers. Headquartered in Reston, Va., Leidos reported annual revenues of approximately $11.09 billion for the fiscal year ended January 3, 2020. For more information, visit . Pay and benefits are fundamental to any career decision. That's why we craft compensation packages that reflect the importance of the work we do for our customers. Employment benefits include competitive compensation, Health and Wellness programs, Income Protection, Paid Leave and Retirement. More details are available here . Leidos will never ask you to provide payment-related information at any part of the employment application process. And Leidos will communicate with you only through emails that are sent from a Leidos.com email address. If you receive an email purporting to be from Leidos that asks for payment-related information or any other personal information, please report the email to . All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws.

About AbbVie AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . on Twitter , Facebook , Instagram , YouTube and LinkedIn . Summary: The Sr Mechanical Engineer will work collaboratively with a team to design and develop medical products from initial concept through the transfer to production. The engineer will have a technical leadership role for designing and testing components and subassemblies of the overall system product. The job requires excellent CAD skills, design of plastic injection molded parts and machined metal components, development and execution of tests for evaluation and verification. Expertise in design of sheet metal enclosures is desired. The engineer should have broad knowledge of plastic and metal materials and be able to define the selection criteria and tradeoffs for different materials. Skills for thermal or structural analysis as well as statistical analysis are needed. Essential Duties and Responsibilities include the following (other duties may be assigned.): Act as a technical lead for product development projects. Provide mentoring and guidance to other team members. Manage the overall development of parts and subassemblies for a project design. Interact with Clinical and Marketing departments to determine design requirements and goals. Outline and execute to short-term goals to achieve overall project milestones. Conceive, design, build, and evaluate prototypes to explore a range of design concepts. Prepare, present, and document designs at technical reviews. Refine and develop selected concept(s) with little guidance from manager. Investigate and evaluate materials, adhesives, and assembly techniques based product requirements and based on past experience. Select vendors for prototypes, request quotes and prepare purchase requisitions. Provide recommendations for production vendors. Use best methods of design for manufacture and assembly (DFMA) and document the DFMA benefits of the chosen design. Plan, perform, and document verification testing. Coordinate testing by other team members, Help develop assembly procedures and assist in transfer methods to manufacturing. Document ECO changes within the Document Control system. Coordinate design tasks for other team members for complex product designs. Coordinate design constraints within ME team and other R&D groups. Resolve any design conflicts with preferably no managerial intervention. Products under development are likely to include: Injection molded plastic parts, mechanical layout of flex circuits, elastomeric components, machined or sheet metal fabricated components (including brazed or welded components), films, electrical connectors and cables use of force, and temperature sensors, design of seals for fluid systems Qualifications • BS in Mechanical Engineering or equivalent degree. Advanced degree desirable. • Must have at least eight years of product design and development experience; prefer ten years of experience. • Prefer at least three years of experience in medical devices, ideally class II devices. • Must be proficient with 3D CAD modeling; prefer Pro/E Wildfire/Creo experience or SolidWorks. Needs some CAD analysis skills for thermals and structures. • Must be familiar with the capabilities and limitations of a variety of fabrication techniques (e.g. plastic injection molding, vacuum and pressure forming, sheet metal, stamping, machining). • Individual will complete work with minimal supervision of the manager. Will typically be the technical leader. • Proficient with basic standard concepts and constraints involved in creating new product designs. Should be knowledgeable of new modern methods for making prototype or production parts. • Ability to set medium term project goals and outline schedules for multiple tasks for several team members. • Strong team player with the demonstrated abilities and willingness to wear "multiple hats" and perform a wide range of tasks within a dynamic environment. • Individual must have strong verbal and written communication skills. Additional Requirements: • Responsible for performing all duties in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies. Language and Verbal Skills: Ability to read, analyze, and interpret engineering specifications, general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, specifications, business correspondence, and procedure manuals in English. Ability to effectively present information and respond to questions from groups of managers, clients, and customers. Ability to clearly and concisely convey project accomplishments, obstacles, issues, and project status. Math Skills: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in complicated, advanced engineering or mathematical formats. Analytical and Reading Skills: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to analyze a variety of technical instructions in mathematical or diagram form and interpret various abstract and concrete variables. Ability to read technical and clinical literature and documents and extract important concepts. Physical Requirements: The physical demands and work environment described here are representative of those an employee encounters while performing 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 regularly required to sit, stand, walk, talk and hear; typically for 8 hours per day. The employee is regularly required to lift and carry up to 10 pounds and occasionally lift and carry up to 25 pounds. Duties also involve daily keyboard data entry. Specific vision abilities required by this job include close vision. Work Environment: Most work is performed in an office-like setting. The noise level in the environment is usually low to moderate. Typically the employee will need to spend about 40 hours per week to complete assigned tasks but that may increase during critical project times. Most work will be done on site to facilitate the collaborative nature of the product development process. Requires some presence in a (clinical or engineering or animal) laboratory setting where protective equipment or other health and safety measures and training are required to protect against chemical, biological or other hazards.. Short duration domestic travel may be required quarterly or semi-annually to visit vendors or customer sites. Limited international travel may be required. Safety: Allergan/Zeltiq is committed to the health and safety of our employees. We expect that all employees will perform their responsibilities while maintaining a safe, cooperative, and productive work environment, thus ensuring the health and safety of themselves and others. Significant Work Activities Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

Process Engineer - Injection Molding Salary Up to $110,000 + Bonus & Benefits & Paid Relocation to the USA Mid-West This Process Engineer position requires a hands-on team player who will provide their technical expertise for instructing and guiding others on the processes and procedures. You'll analyze systems to solve production problems and will take action to maximize manufacturing process and improve efficiencies, quality, and timeliness of product. In this position, you would make recommendations on tooling size, design, and shape. Support production facilities with cycle time improvements. Utilize LEAN Manufacturing, statistics, SPC, Six Sigma, 5S, problem solving, and root cause analysis. Implement Preventative maintenance planning procedures. Work closely with the design team on concept design and improvements. Consults on business process engineering, process measurements, change management, education and training and identifies opportunities for business process improvement. Salary Up to $110,000 + Bonus & Benefits & Paid Relocation to the USA Mid-West This opportunity is in the heart of the Midwest. You'll be in a bustling town located in beautiful countryside with lush greenery and rivers. Picturesque in every season and temperate weather - a beautiful White Christmas that melts into spring! The area boasts one of the best downtowns around, college & pro sports, state fairs, local festivals, access to higher education, fabulous food, shopping & entertainment for the whole family! Wonderful area to raise a family and jump your career into overdrive. Job Requirements: Requirements for this Process Engineer position: ● Technical, AAS, or BS degree in Engineering, OR equivalent experience ● At least 5 years' process engineering experience, preferably in plastics ● Husky injection experience would be a plus ● Experience with Polyethylene Terephthalate (PET, PETE, or polyester) is a plus. TO APPLY: Email your resume OR jeannieATaustinallenDOTcom in MS Word or PDF ( please remove the capital letters and replace with proper symbols ) . * All Interview, relocation, & fee expenses paid by hiring companies. Hiring companies offer excellent compensation packages, benefits, and generous relocation assistance or packages. Areas of Specialization... * Engineering * Six Sigma Black Belts * Accounting * Distribution * Human Resources * Materials / Purchasing * Quality Engineers & Managers * Manufacturing Management

Position Summary The Senior Development and Sustaining Engineer is responsible for the development and maintenance of respiratory, anesthesia, and/or urological products. Under minimal direction, the incumbent will organize and manage multiple projects and ensure they are completed in a timely manner, create design ideas for new products, and develop creative solutions to existing products when problems arise or modifications are requested. Principal Responsibilities Conduct research and/or development projects associated with the design and/or modification of medical devices, components, models, or mechanisms. Prepare or coordinate formal documentation of the product designs, risk analysis, product specifications, market specifications, etc. according to established product development procedures. Initiate formal reviews to get approvals per procedures. Develop, maintain and publish product development plans for assigned projects with critical milestones and timelines. Develop and coordinate the running protocols for the validations of new or modified devices or components, including validations of the design, manufacturing process, assembly, packaging, and sterilization where applicable. Investigate and resolve technical problems involving product performance, production equipment, or facility systems affecting production. Coordinate the product design and development process with appropriate support departments such as engineering, regulatory, documentation, tooling, and manufacturing. Serve as project leader for assigned projects and follow up on all aspects of projects, including conducting reviews with support groups and outside resources where applicable. Prepare or follow up on preparation of design drawings, specifications, estimates of costs, mainframe updates, etc. Discuss and consult with sales staff or customer on product requirements and specifications where design or manufacturing problems are involved. Work with manufacturing in the justification and the selection of the manufacturing process. Assign projects and establish priorities to ensure datelines and goals are achieved. Develop assembly methods and procedures. Create engineering draws and specifications. Coordinate changes in process, tolling, and equipment identified to positively impact the manufacturing process, while staying within GMP guidelines. Coordinate the reporting on project status for all responsible projects. Direct reports in formal periodic project review meetings, to include cost reduction progress, capital spending, and expense status. Enhance personal growth and development through participation in education programs, current literature, training meetings and workshops. Participate actively in continuous quality improvement activities through compliance with safety standards. Demonstrate professional responsibilities by cooperating with other personnel to achieve department and interdepartmental goals and objectives and maintain good employee relations. Organize, evaluate, and coordinate engineering studies with professional, technical, and clerical staff of a product evaluation department. Analyze complex, technical and administrative problems and adopt an effective course of action. Conduct comprehensive studies and preparation of reports including recommendations. Make effective presentations to, and participate in, a variety of meetings and conferences with other companies and the public. Prepare clear and concise statements and reports. Education / Experience Requirements Bachelor s degree in Biomedical Engineering or closely related field. Possession of BS degree may be substituted for six (6) additional years of work experience in the design and/or modification of plastic components for the medical industry 5+ years experience in product development 3+ years experience leading medical device engineering projects Experience with injection molding, plastic extrusion and plastic part assembly process and methods required Experience with CAD (design/drafting) programs, including SolidWorks, preferred Specialized Skills / Other Requirements Solid understanding of and experience with: U.S. FDA GMP and ISO requirements for the design, validation, manufacturing processes, secondary operations and assembly of medical components and devices. ISO and ASTM testing methods for medical devices and general plastic components Principles and practices of professional engineering. Regulations pertaining to medical device design and design modifications. Demonstrated creativity and ingenuity in applying engineering principles and practices and drawing solutions from a wide range of experience. Effective written and oral communication skills and ability to present information to, and respond to questions from, various audiences. Ability to interpret and follow instructions furnished in written, oral, diagram, or schedule form. Intermediate knowledge of Microsoft Office Suite (Project, Word, Excel, and Access) Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Proven ability to establish and maintain effective working relationships with peers. Working Conditions / Physical Demands Typical research lab and office environment; occasional work in manufacturing areas and some field work. Some exposure to the electrical/mechanical/power manufacturing or testing equipment, with occasional heat and noise exposure and exposure to dust. May visit domestic and international (Mexico, Asia) manufacturing sites. Travel required up to 10%. Associated topics: boiler, catia, mechanical, mechanism, motor, powertrain, proe, rotordynamic, turbine, vibration

Amick Brown is seeking an experienced Mechanical Engineering Drafter/Designer for our direct client. Location : Sunnyvale, CA Duration : 6 Months Job Role The Mechanical Engineering drafter/designer will assist product engineering, manufacturing engineering, and other engineering teams by providing CAD drafting and design support to create/revise drawings for new/legacy custom parts, designing and/or modifying new/legacy custom components in CAD, and by reviewing dimensions and tolerances on drawings to ensure their suitability for the intended production process. The successful candidate will have the technical depth and proven experience to create and review drawings to ASME Y14.5 standards. Candidate must have experience with Windchill for CAD data management. Candidate will demonstrate knowledge of GD&T and the use of CAD tools to create/refine designs and drawings for assemblies and custom parts made of sheet metal, weldments, various plastics - some with complex surfaces, castings, electrical cables/components, and machined parts. The candidate will be a team player, collaborate with engineering teams, and have a strong sense of responsibility and commitment towards producing accurate drawings. Job Responsibilities Work with various teams to identify drafting/design support needs and schedule workload based on priorities set by management Identify scope of design/drafting support needs requested by engineering teams Estimate time required to complete support activities Provide CAD design/drafting support as needed Communicate with vendors to determine process capabilities to verify manufacturability of part to tight dimensions/tolerances Support Product Engineering with creation and submission of ECOs Communicate with engineering teams to review drawing changes to suit manufacturing process capabilities Communicate designs and design changes with vendors and assist with DFM updates Work from rough sketches and specifications created by engineers to design static aids and dynamic fixtures used in testing and manufacturing of product Assist in creating engineering BOMs on drawings and in MRP systems Assist in lifecycle changes and production release of drawings via ECOs Provide mechanical engineering support for resolution of field and manufacturing issues via drawing changes Establish individual goals consistent with team goals and project schedules Required Skills Associates degree in Mechanical and/or Industrial engineering required Minimum of 5 years of experience in creating drawings for mechanical parts, electro-mechanical assemblies, tooling components, and electrical cable assemblies Some experience in creating parametric shapes using surface modelling Experience in creating assembly drawings of mechanisms and drawing BOMs Experience with drawing reviews/checking Understanding of dimensional tolerance capabilities of process such as injection molding, castings, machine parts, and sheet metal components. Proven experience in a fast paced, high transaction environment Proven ability to work well in a team environment Proficiency using CAD to design and document mechanisms in SolidWorks Proficiency using Windchill PDM for file management Knowledge of ProE is beneficial Knowledge of component finishing processes such as electro-polishing, plating, heat treatment, paint/powder coating) Amick Brown is an Information Technology consulting company specializing in ERP, Data Analytics, Information Security, Application Development, Networking, and Cloud Computing. The company was founded in 2010 and is headquartered in San Ramon, California. Regular full-time employees are eligible for the following Amick Brown provided benefits: Health Vision Dental 401k with company match Paid time off Sick Leave Short-Term Disability Life Insurance Wellness & Discount Programs - provided by Dice