- Amgen (Cambridge, MA)
- …various global manufacturing sites. This role requires a deep understanding of medical device design, manufacturing processes, and regulatory requirements. Key ... years of progressive experience as an engineer or scientist in relevant fields ( medical device development, manufacturing, etc.) + Proven track record of… more
- Fresenius Medical Center (Lawrence, MA)
- …REQUIRED SKILLS** + Minimum 7+ years' experience in electrical product development, medical device or highly regulated product development preferred. + ... such as FTA and FMEA to ensure design and process shortcomings are identified and appropriately addressed. + Support...including specification, documentation, and quality assurance + Experience in medical device safety and EMC compliance (IEC… more
- Amgen (Cambridge, MA)
- …automate model creation and post/processing. + Experience with combination products and device regulatory requirements, medical device development and design ... the world. In this vital role you will apply engineering principles to develop efficient and trustworthy models addressing...to create models capturing the inherent variability in the process and device dimensions. + Skilled in… more
- …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... looking for a Motivated Engineer to join our Semiconductor Process Team in North Reading, Massachusetts to develop, qualify,...minimum criteria for the position. + Bachelor's degree in EE/ engineering technology/Optical, or a related field + 1 to… more
- Fresenius Medical Center (Lawrence, MA)
- …alignment across the organization. + Provide planning and project management support for medical device product launches. + Assist in the development and ... years of experience as a Product Manager in a medical device field or (ii) Master's degree...device field or (ii) Master's degree in Biomedical Engineering or Bioengineering. Must also have had experience (which… more
- Abbott (Burlington, MA)
- …types of product complaints. Independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory ... on product complaints to various teams (eg Regulatory, Quality Engineering ). The other role of the Post Market Surveillance...work experience **Preferred Qualifications** + 3+ years in MDR ( Medical Device Reporting) + Knowledge of the… more
- Fresenius Medical Center (Lawrence, MA)
- …Quality Business Partner for Software as a Medical Device and Non- medical software device engineering teams to ensure compliant products, ... compliance. . Reviews and approves design control deliverables along the product development process as well as design changes . Partners with and/or guide software… more
- Capgemini (Burlington, MA)
- …verification strategies, manage a team of engineers, and ensure compliance with medical device regulations. **Your Role** . Lead Verification Strategy: Develop ... & Standards: Ensure all verification activities align with relevant medical device regulations such as ISO 13485,...a plus. . Bachelor's or master's degree in computer engineering , Electrical Engineering , Biomedical Engineering ,… more
- Fresenius Medical Center (Lawrence, MA)
- …for staffing and leading a team of software developers to deliver high quality medical device software. Develop and drive a long-term strategic vision for the ... in software development, verification, and standards necessary to meet global medical device regulatory requirements. + Clear understanding of Software… more
- RTX Corporation (Andover, MA)
- …/tool outputs and device /product performance and yield. + Teaming with materials, process , equipment, design, and layout engineering teams to solve a wide ... teams. + Engagement in technical communities related to semiconductor manufacturing and device engineering **What We Offer** Our values drive our actions,… more