- ThermoFisher Scientific (Ward Hill, MA)
- …Proven ability in a Quality Assurance position within the Chemical, Medical Device or Pharmaceutical Industries supporting Regulated Products. + Minimum 2-3 ... **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** Quality Manager US Full-Time Internal/External When you join Thermo… more
- Medtronic (Billerica, MA)
- …metal precision processing, and adhesives for the Catheter/Disposable SQE position. + Medical device manufacturing industry experience, preferably ISO 13485. + ... skills and ability to lead cross-functional teams. + In-depth knowledge of quality systems, standards, and regulatory requirements. + Excellent communication and… more
- Consolidated Precision Products (Burlington, MA)
- …materials and escalate findings according to Standard Operating Procedures (SOPs) and regulatory or customer quality standards. + Perform visual inspections ... We deliver high-performance products that meet the rigorous demands of quality , durability, and precision required for next-generation turbine engines while helping… more
- Curia (Hopkinton, MA)
- …to 8 years' experience in Quality Assurance in the pharmaceutical/biotechnology or medical device industry experience, including 2 years in a leadership role ... SUPERVISOR, QUALITY ASSURANCE in Hopkinton, MA Build your future...inspections and registrations + Participate in client audits and regulatory inspections, implement audit commitments + Participate in client… more
- ICON Clinical Research (Boston, MA)
- …for the conduct of research involving human subjects is required in the medical device industry. + Helps to review project documentation and deliverables ... of Clinical Research or equivalent. + Minimum 3 years of experience in Medical device , pharmaceutical industry, or other regulated environment experience is… more
- Takeda Pharmaceuticals (Boston, MA)
- …communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs, Quality Assurance, Medical Affairs, Marketing, ... the Company-wide patient safety expert for assigned pharmaceutical / biological / drug- device combined products, accountable for the safety strategy and major safety… more
- Fresenius Medical Center (Lawrence, MA)
- …geometric tolerance analysis, and documentation is preferred + Strong understanding of medical device development processes + Able to communicate effectively, ... and/or testing of complex electro-mechanical products preferred + Prior medical device experience strongly preferred EO/AA Employer:… more
- Fresenius Medical Center (Lawrence, MA)
- …accountable for staffing and leading a team of software developers to deliver high quality medical device software. Develop and drive a long-term strategic ... + Experience in software development, verification, and standards necessary to meet global medical device regulatory requirements. + Clear understanding of… more
- Bausch + Lomb (Boston, MA)
- …Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and Clinical ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… more
- Beth Israel Lahey Health (Watertown, MA)
- …protocols and CAP regulatory requirements. Performs, evaluates and documents Quality Control activities and device calibration. (essential) 2. Communicates ... Also performs an array of moderate complex laboratory tests, performs daily quality controls on all lab devices, confirms accurate results, reports results to… more