- Hologic (Marlborough, MA)
- …minimum of 8 years of experience in Regulatory Affairs within the Medical Device industry. + Experience authoring/supporting/maintaining SOPs. + Deep ... in regulatory practices. This role will execute in the development and implementation of global regulatory systems, support regulatory...understanding of global medical device and/or IVD regulations. + Experience… more
- Bausch + Lomb (Boston, MA)
- …areas of Responsibility** **:** Clinical Operations: + Manage and/or oversee the development process for critical study documents (eg, protocol, amendments, IB, ... over our 170-year history. We have a significant global research, development , manufacturing and commercial footprint of approximately 13,000 employees and a… more
- RTX Corporation (Andover, MA)
- …have the opportunity to work closely with engineers from multi-disciplined teams to analyze device , process , and circuit data from our GaN and GaAs foundry. Some ... monitoring data + Analysis of integrated circuit or device performance data + Tracking of process ...Support the wafer foundry team including both production and development efforts + Support the design, development ,… more
- Teradyne (North Reading, MA)
- …and presentation skills. + Comfortable and familiar with peer reviewed software development process . + Comfortable working with open source communities (Linux ... powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device… more
- Fujifilm (Boston, MA)
- …and advertising regulations and other regulations specific to Life Sciences/Pharma and Medical Device companies. + Perform other duties as assigned. **Required ... corporate law firm and/or in-house legal department, preferably in the Life Sciences/Pharma, Medical Device or health care field. + Solid commercial contract… more
- Tecomet (Woburn, MA)
- …root cause elimination is completed for identified issues. + Manage the Complaint Handling process and Medical Device Reporting activities. + Oversee the ... and standards requirements and support RA staff in filing process . + Review, analyze and approve technical data generated...development of quality systems for a highly regulated medical device , aerospace, defense industries to achieve… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of current global Good ... Japanese arm. + Previous experience of working in the global pharmaceutical and medical device industry. + Experience working with external service providers. +… more
- Teleflex (Chelmsford, MA)
- …and audit participation. A strong background in quality assurance within the medical device industry, along with excellent organizational and communication ... 10% **Requisition ID** :12481 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health… more
- Medtronic (Boston, MA)
- …Sales, Marketing, Strategy or Business Development in a highly regulated industry ( Medical Device , Aerospace, etc.) + 7+ years of experience working in the ... support the establishment of Customer Success initiatives, inclusive of process , metrics, and communication in US This position will... medical device industry in a role that… more
- Hologic (Marlborough, MA)
- …+ MBA preferred. **Experience** + 7+ years of experience in marketing within the medical device , diagnostics, or healthcare field required + 3+ years of direct ... strategy. The ideal candidate brings extensive product management experience in med device , and will be responsible for both product lifecycle activities and US… more