- Olympus Corporation of the Americas (Center Valley, PA)
- …of 6 years of experience. + Prior experience in a sponsor, CRO, or medical device company. In-depth knowledge and experience with FDA regulations and familiarity ... and GCDMP. + Strong expertise in implementing and maintaining systems for global medical device trials (Class II/III or combination products). + Excellent… more
- WellSpan Health (Chambersburg, PA)
- …leadership roles and identifies Manager on Call. 8. Participates in MOCK, medical emergencies and/or RRT. 9. Demonstrates ability to perform CIWA, AIMS, DAST/AUDIT, ... staff by: complying with all applicable safety regulations; learning the impact of medical errors and methodology that will lead to reduction of errors; reporting… more
- Hologic (Marlborough, MA)
- …concept through to production and manufacturing transfer. + Exposure to regulatory and quality requirements within the medical device industry is ... practices relevant to biomedical or mechanical product development, particularly in the medical device industry. + Knowledge of manufacturing processes such as… more
- Actalent (San Clemente, CA)
- …+ Advanced degree (Master's or Ph.D.) preferred. + 5+ years in the medical device industry focusing on biocompatibility, regulatory compliance, or quality ... The Quality Assurance Specialist will lead the evaluation of medical devices against biological evaluation standards. This role involves reviewing real-world… more
- ManpowerGroup (Peachtree Corners, GA)
- Our client, a leading medical device company, is seeking a Material Handler I to join their team. As a Material Handler I, you will be part of the Warehousing ... + Possess high school degree or GED. + Strong interpersonal skills. + Medical device experience preferred. + Experience and/or certification in operating… more
- ManpowerGroup (Cypress, CA)
- Our client, a leader in the medical device industry, is seeking a 2nd Shift Medical Device Assembler to join their team. **Job Title:** 2nd Shift ... Medical Device Assembler **Location:** Cypress, CA **Pay...OSHA standards. + Comply with company policies, procedures, and quality standards. + Communicate any stoppages on the line… more
- Terumo Neuro (Aliso Viejo, CA)
- …Responsible for leading and managing complex chemistry related projects in medical device product development, production, and maintenance. Design and ... + Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as...of six (6) years of relevant chemical, pharmaceutical, and/or medical device manufacturing experience. 3. Strong written… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- …threats and advises relevant stakeholders on appropriate courses of action. + Evaluate medical device security protocols, including IoT and biomedical device ... Leadership and/or CISO role. + Strong background in healthcare cybersecurity, especially medical device ecosystems + Experience with developing, socializing, and… more
- US Tech Solutions (Waco, TX)
- …European Community (EC), ISO 13485 - Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations ... (7) years of experience in either ** Quality Control/ Quality Assurance** functions within the ** device , food, or cosmetic industry.** **What are the top 3-5… more
- Cordis (Miami Lakes, FL)
- …team. This role will focus on polymer and fluoropolymer extrusion for critical medical device components and catheter shaft assemblies. The ideal candidate has ... with extrusion process development, optimization, and validation in a regulated medical device environment. **Key Responsibilities** + Develop and optimize… more
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