Quality Management Systems

Biogen

Cambridge, MA · $138,000 – $185,000

This senior leadership role focuses on ensuring quality and regulatory compliance for medical devices and combination products throughout their lifecycle. It suits experienced quality engineers who are comfortable guiding cross-functional teams, managing supplier relationships, and driving continuous improvement in highly regulated environments.

Listed on Biogen’s careers site · Apply there ↗

Adient

Lead quality management and continuous improvement for automotive seat cover manufacturing across multiple plants, overseeing compliance with IATF 16949 standards, customer requirements, and supplier quality programs. This role suits experienced quality professionals who can drive operational excellence through Lean and Six Sigma methodologies while managing cross-functional teams and customer relationships.

Listed on Adient’s careers site · Apply there ↗

The Hershey Company

Bluffton, IN

This role leads sanitation and cleaning operations across a food manufacturing facility, ensuring compliance with food safety certifications and regulatory standards. It suits supervisory professionals with food safety knowledge who can manage teams, drive process improvements, and maintain strict hygiene and quality protocols in a production environment.

Listed on The Hershey Company’s careers site · Apply there ↗

Medtronic

Lead quality assurance for Medtronic's medical device distribution operations across Korea, India, and Southeast Asia, managing a team of five QA professionals and ensuring compliance with regulatory and internal standards. This role suits experienced quality professionals in regulated industries who can oversee complex supply chain compliance and drive process improvements across multiple regions.

Listed on Medtronic’s careers site · Apply there ↗

Merck

Full-time · $156,900 – $247,000

This role leads quality and standards initiatives across a pharmaceutical company's medical affairs and outcomes research division, working in a global matrix environment to create, maintain, and align operational standards with regulatory and compliance requirements. It suits experienced professionals with healthcare or life sciences backgrounds who excel at cross-functional project leadership and thrive in complex, ambiguous settings.

Listed on Merck’s careers site · Apply there ↗

Bristol Myers Squibb

Full-time · Indianapolis, IN · $141,515 – $171,483

This senior operations quality assurance role oversees compliance and quality activities across manufacturing and supply chain functions at a radiopharmaceutical manufacturing site, managing up to 8 staff members. The position suits experienced quality professionals with deep FDA/EMA regulatory knowledge and hands-on shop-floor expertise who can lead teams through complex manufacturing challenges in a fast-paced biotech environment.

Listed on Bristol Myers Squibb’s careers site · Apply there ↗

Moderna

Full-time · $224,900 – $404,600

This executive role leads Moderna's quality assurance strategy across all research and development phases, from early research through late-stage clinical trials. It suits seasoned quality leaders with deep regulatory expertise who want to shape organizational culture and modernize QA practices at a pioneering mRNA medicines company.

Listed on Moderna’s careers site · Apply there ↗

Gilead Sciences

Full-time · United States - California - Foster City · $157,590 – $203,940

This role manages Gilead's global quality agreement program as a subject matter expert, handling template development, regulatory compliance, and stakeholder collaboration across manufacturing partnerships. It suits experienced quality professionals with strong regulatory knowledge who can lead complex cross-functional initiatives in a highly regulated pharmaceutical environment.

Listed on Gilead Sciences’s careers site · Apply there ↗

Arianespace / ArianeGroup

Full-time · Taufkirchen

This quality inspector role involves inspecting aerospace components and systems during manufacturing and accepting them for delivery at ArianeGroup's Ottobrunn facility. It suits someone with technical training and several years of quality assurance experience who is comfortable with documentation, standards compliance, and working in a precision manufacturing environment.

Listed on Arianespace / ArianeGroup’s careers site · Apply there ↗

Eight Sleep

Full-time · San Francisco, CA

Eight Sleep is hiring a Director of Regulatory Affairs and Quality Assurance to lead compliance, risk management, and FDA regulatory strategy for their medical-device sleep technology platform. This role suits experienced medical device professionals ready to shape regulatory practices at a growth-stage company with direct access to leadership and R&D.

Listed on Eight Sleep’s careers site · Apply there ↗