Quality Jobs

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Sr. Quality Engineer Post Market Surveillance
GermantownUS$110000 - US$127000 per year

Join a globally renowned innovator in medical devices who is seeking an expert senior quality engineer to join their team. Recently, the company received FDA approval for its latest device focusing on diabetes, which offers unparalleled accuracy and convenience for glucose management. Be part of a team that is creating breakthrough technology to tr...

Director of Quality (GLP/GCLP)
Pleasanton, CaliforniaUS$150000 - US$200000 per year

A rapidly growing bioanalytical CRO to support their search for a Director of Quality Assurance. This is a leadership role where you'll drive the development and continuous improvement of GLP and GcLP quality systems supporting both nonclinical and clinical testing. You'll be the face of Quality during client and regulatory inspections, help shape ...

Sr. Manager, Supplier Quality
TrumbullUS$121000 - US$175000 per annum

🚀 Now Hiring: Senior Manager, Supplier Quality | Lead the Future of Women's Health InnovationAre you a seasoned quality leader ready to make a meaningful impact in the medical device and fertility space? We're looking for a Senior Manager, Supplier Quality to join a mission-driven organization that's transforming women's healthcare and assisted re...

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Selby Jennings Start Your Career In Recruitment
Director of Laboratory Services
San AntonioUS$125000 - US$160000 per year

Director, Laboratory Services - Infectious Disease TestingLocation: San Antonio, TexasSalary: $145,000 - $170,000 + bonus + excellent benefits + relocation assistance Position Overview: Lead and manage laboratory services to ensure efficient operations that meet or exceed quality standards. Implement Lean Six Sigma or other methodologies to drive p...

MES Validation Engineer
PhiladelphiaNegotiable

This role will be working across global manufacturing sites, ensuring quality and compliance is fully embedded into the MES through standardizing quality processes, validation approach and digital batch record structures. The ideal candidate will have strong quality and compliance expertise with a deep understanding of MES systems. Key Responsibili...

Quality CAPA Consultant
HuntersvilleNegotiable

Key Responsibilities: Develop, implement, and maintain CAPA processes in compliance with FDA 21 CFR Part 820 and ISO 13485 standards.Conduct thorough investigations to identify root causes of nonconformities and quality issues.Collaborate with cross-functional teams to develop and implement effective corrective and preventive actions.Monitor and an...