- Pfizer (Kalamazoo, MI)
- …directly impact patients. **ROLE SUMMARY** Responsible for implementation of Kalamazoo site Quality Systems for Medical Device /Combination Products. Supports ... for medical devices and combination products. Ensures inspection readiness and compliance with all applicable medical device and combination product… more
- Abbott (Maple Grove, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...to manage implementation projects for emerging regulations and lead/drive quality compliance metrics for the Regulatory shared… more
- AbbVie (North Chicago, IL)
- … Assurance, Regulatory, Operations, or Technical Support in a pharmaceutical or medical device setting required. Experience working in a regulatory agency ... Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose The Associate Director, Global Quality and Compliance Excellence uses advanced subject matter… more
- Integra LifeSciences (Braintree, MA)
- …in Engineering, Life Science, or a related field with 5+ years' experience in QA/ Compliance within the medical device or similar industry or equivalent ... and making headway to help improve outcomes. The Senior Quality Compliance Specialist -Training will create and...enhance the skills and competencies of employees in a medical device -regulated environment. The Senior Training Specialist… more
- Abbott (Maple Grove, MN)
- …Registration support + Ad and Promotional Material - Regulatory Review + EU and US medical device compliance + Project management skills - organize and host ... for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more… more
- J&J Family of Companies (Santa Clara, CA)
- …on projects while staying in compliance with FDA, ISO, EU, and other applicable medical device regulations as well as SWMI Quality System requirements. + ... improvement opportunities. + Audit production lines to ensure QSR/GMP compliance as assigned. + Maintain audit readiness of the...**Requirements** + 2+ years of supervisory experience in the Quality function in the medical device… more
- Terumo Medical Corporation (Somerset, NJ)
- …Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad range of applications ... Healthcare Compliance Contract Specialist Date: Jul 23, 2025 Req...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
- Philips (Plymouth, MN)
- …**You're the right fit if:** + Experience in regulatory affairs, quality compliance , product development or equivalent in the medical device industry ... Devices business by coordinating regulatory activities and ensuring products meet relevant medical device standards and requirements. **Your role:** + Assists in… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …3 years in Quality Assurance in the pharmaceutical, biopharmaceutical, or medical device industry, or a combination of education and experience. Knowledge ... Quality Compliance Specialist Department: Quality Location: Monroe, NC START YOUR APPLICATION… more
- US Tech Solutions (San Bruno, CA)
- … System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation and ... and support CAPA, complaints, audits, and overall QMS functions. **Experience:** ** Medical Device Software Experience:** 1. Proven experience in software… more
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