Corrective And Preventive Action (CAPA)

AST SpaceMobile

Midland, TX

This role involves designing and implementing a unified quality management system across an aerospace manufacturer's multiple locations, with a focus on achieving AS9100 certification. It suits experienced compliance professionals who have led initial QMS implementations in regulated industries and want to build quality infrastructure from the ground up rather than maintain existing systems.

Listed on AST SpaceMobile’s careers site · Apply there ↗

Crusoe

Full-time · Brighton, CO · $190,000 – $215,000

This role oversees the design and operation of a Quality Management System across Crusoe's manufacturing facilities, ensuring compliance with standards like ISO 9001 and driving continuous improvement as the company scales. It suits someone with deep QMS expertise and audit experience who can translate quality frameworks into practical controls and lead cross-functional teams in a fast-growing manufacturing environment.

Listed on Crusoe’s careers site · Apply there ↗

Jabil

Full-time · Florence, KY

A quality engineer role at a major manufacturing company focused on ensuring product compliance and driving continuous improvement through audits, corrective actions, and risk management. This suits experienced quality professionals ready to work night shifts and lead quality initiatives in a high-volume production environment.

Listed on Jabil’s careers site · Apply there ↗

KLA-Tencor

Full-time · Ann Arbor, MI · $86,700 – $147,400

This role supports quality consistency across KLA's global supplier network by monitoring performance, conducting audits, and driving continuous improvement in precision manufacturing environments. It suits engineers with supplier quality or manufacturing quality experience who want to influence product reliability and supplier relationships at a leading semiconductor equipment maker.

Listed on KLA-Tencor’s careers site · Apply there ↗

Hims and Hers

Full-time · Minnetonka, MN · $130,000 – $170,000

This role oversees contract manufacturing operations for FDA-regulated medical devices, serving as the technical liaison between internal teams and external manufacturers. It suits experienced process engineers with deep medical device manufacturing expertise who can manage complex regulatory compliance and drive operational excellence across suppliers.

Listed on Hims and Hers’s careers site · Apply there ↗

Crane Co.

Piqua, OH

This role owns the quality management system and leads continuous improvement efforts in a manufacturing environment, including CAPA processes, root cause investigations, and supplier quality. It suits someone with 2–3 years of quality or manufacturing experience who wants to grow technical expertise in process control and quality systems.

Listed on Crane Co.’s careers site · Apply there ↗

Beckman Coulter

Full-time · Duncan, SC

This quality engineer role focuses on managing product complaints, non-conformances, and corrective actions in a regulated manufacturing facility. The position suits someone with an engineering background and manufacturing experience who enjoys solving problems across teams and driving continuous improvement.

Listed on Beckman Coulter’s careers site · Apply there ↗

Biogen

Full-time · Cambridge, MA · $188,000 – $259,000

This director-level role leads a team building data systems and intelligence to monitor risks across Biogen's manufacturing and supply network, translating complex operational data into executive guidance for strategic decisions. The position suits experienced analytics leaders with deep pharmaceutical manufacturing knowledge who can combine technical rigor with clear stakeholder communication.

Listed on Biogen’s careers site · Apply there ↗

Moderna

A senior quality assurance role leading pharmaceutical manufacturing oversight at Moderna's Melbourne facility, focused on validation, process compliance, and regulatory readiness for mRNA drug production. Suits experienced pharma quality professionals who thrive in complex, regulated environments and want to drive operational excellence while supporting rapid innovation.

Listed on Moderna’s careers site · Apply there ↗

Bristol Myers Squibb

Full-time · $124,449 – $150,803

This role manages supplier quality and compliance for a biotech company developing radiopharmaceutical therapies, overseeing vendor qualifications, material lifecycle management, audits, and regulatory adherence across manufacturing operations. It suits someone with quality assurance experience in regulated environments who can lead cross-functional teams and navigate complex vendor relationships in a GMP-controlled setting.

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