- Cognizant (Boston, MA)
- …cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the ... program Awareness of Electronic Lot History Records using Camstar Software for Medical Device / Pharma industries Implement and execute the shopfloor transaction… more
- Hologic (Marlborough, MA)
- …R&D Clinical Affairs team and contribute to the development of groundbreaking medical device technologies that transform patient care. The successful candidate ... will lead clinical development activities, working cross-functionally to generate high- quality clinical evidence that supports regulatory clearance, market… more
- Veterans Affairs, Veterans Health Administration (Jamaica Plain, MA)
- …handling. Performs assigned clinical procedures, such as; application of External Urinary Device 's (EUD) and colostomy bags, unsterile soaks and compresses, hot and ... Performs assigned technical procedures, such as blood glucose monitoring and quality controls, EKG's, taking and recording blood pressure, temperature, pulse,… more
- Teleflex (Chelmsford, MA)
- …Demonstrated leadership experience. * Familiarity with QSR/ISO regulations and standards for medical device manufacturing. * Proven success in driving employee ... :12539 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to...driven by our purpose to improve the health and quality of people's lives. Through our vision to become… more
- Abbott (Westford, MA)
- …of education and work experience + Manufacturing engineering experience preferred + Medical device experience preferred + Strong analytical, problem solving and ... quality , cost and delivery performance of St. Jude Medical Operations + In conjunction with the Value Stream...Systems (QMS), + Environmental Management Systems (EMS), and other regulatory requirements + Complies with US Food and Drug… more
- Medtronic (Boston, MA)
- …to meet deadlines. + Advanced degrees including MS, PhD or MBA. * Specific medical device experience in the electrophysiology field. * Previous clinical support, ... + Serve as liaison between cross functional partners (supply chain, R/D, regulatory ) and local in-market marketing organizations. + Manage and monitor regional… more
- J&J Family of Companies (Danvers, MA)
- …of 5 years of experience in equipment engineering, preferably in the medical device manufacturing industry. + Extensive experience with production manufacturing ... Manufacturing Practices (GMP) and ensure that all activities align with company quality standards and regulatory guidelines. + Develop and maintain documentation… more
- Cramer (Norwood, MA)
- …you need a strict eye for detail to ensure our work adheres to regulatory , legal, and medical guidelines. Your day-to-day will include researching, creating, ... who can take direction and work independently-a creative thinker who never forgets regulatory rules-and excited to work closely with internal and external teams to… more
- Danaher Corporation (Shrewsbury, MA)
- …plus if you also possess previous experience in: + Experience in the Bio-Science, Medical Device , or Pharma industries. + Ability to read and understand ... issues, implementing cost-effective solutions, and providing customer-focused support. + Quality and Regulatory Compliance: Align manufacturing processes with… more
- Medtronic (Boston, MA)
- …+ Knowledge in product development, project management, and commercialization in the medical device industry + Strong communication and teamwork skills; must ... Anticipate and mitigate risks, balancing time, schedule, cost, and quality , while adhering to safety and regulatory ...commercial new product delivery in a regulated industry (eg medical , automotive, aerospace, etc.) + High degree of competency… more