22 open listings
Roles posted by organizations here, alongside roles we found on employers’ own careers sites. Crawled roles say so on the card and send you to the employer to apply. Only show organizations on Career App
HH
Sr. Process & Operations Engineer
Hims and Hers
Full-time · Minnetonka, MN · $130,000 – $150,000
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 ↗
Staff Quality Assurance Engineer
Beckman Coulter
Full-time · Indianapolis, IN
This role leads quality assurance processes for medical device manufacturing at a major diagnostics company, managing compliance with regulatory standards and guiding teams through the quality lifecycle. It suits experienced quality engineers who want to influence manufacturing operations and drive process improvements in a regulated industry.
Listed on Beckman Coulter’s careers site · Apply there ↗
Head of Quality, Device and Combination Products
Biogen
Cambridge, MA
Lead the quality strategy and global team for medical devices and combination products at a major biotech company, from design through lifecycle management. This role suits an experienced quality professional with deep regulatory knowledge and demonstrated leadership in device manufacturing compliance.
Listed on Biogen’s careers site · Apply there ↗
A
Manager, Quality Assurance
A-dec
Newberg, OR
This role leads a quality assurance team at a dental equipment manufacturer, overseeing compliance with regulatory standards and driving continuous improvement across the organization. It suits experienced quality professionals with a track record managing teams and implementing quality systems in regulated manufacturing environments.
Listed on A-dec’s careers site · Apply there ↗
Sr. Software Product Owner
Medtronic
Full-time · Boston, MA · $149,000 – $177,600
This role leads product strategy and development for a surgical robotics platform, managing stakeholder coordination and technical requirements across hardware-software systems in a heavily regulated medical device environment. It suits experienced product owners with deep expertise in embedded systems, regulatory compliance frameworks, and scaled agile methodologies who want to shape complex, safety-critical medical technology.
Listed on Medtronic’s careers site · Apply there ↗
Director - Product Quality Complaints
Gilead Sciences
Full-time · United States - California - Foster City · $191,250 – $247,500
This director-level role oversees Gilead's global product quality complaints program, serving as the Global Process Owner for complaint handling across clinical and commercial products. It suits experienced quality leaders in pharma or medical devices who can drive regulatory compliance, process standardization, and cross-functional collaboration in a complex, highly regulated manufacturing environment.
Listed on Gilead Sciences’s careers site · Apply there ↗
AR
Senior Manager, SQE
Agility Robotics
Full-time · Salem, OR · $146,000 – $189,000
Lead supplier quality and incoming material control for a robotics manufacturer, overseeing a team of engineers and technicians while managing global supplier qualifications, audits, and quality systems. This role suits an experienced quality leader with deep expertise in supplier management, advanced product quality planning, and manufacturing operations who can scale operations across complex hardware supply chains.
ISO 13485Failure Mode and Effects Analysis (FMEA)IATF 16949Statistical Process Control (SPC)8D Problem SolvingISO 9001
Listed on Agility Robotics’s careers site · Apply there ↗
ES
Director of Regulatory Affairs and Quality Assurance (RA / QA)
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 ↗
HH
Sr. Product Development Engineer
Hims and Hers
Full-time · Minnetonka, MN · $130,000 – $150,000
This role designs and develops FDA-regulated medical devices and their packaging systems, from initial concept through manufacturing transfer. It suits experienced mechanical or biomedical engineers who are comfortable with regulatory compliance, design documentation, and cross-functional collaboration in a fast-moving healthcare setting.
Listed on Hims and Hers’s careers site · Apply there ↗
Staff Quality Assurance-Supplier Quality Engineer
Beckman Coulter
Full-time · Chaska, MN · $140,000 – $160,000
This is a senior quality engineering role managing supplier transitions and cost-reduction design changes for medical diagnostic equipment at a life sciences company. It suits someone with 12+ years in quality engineering who wants to drive product improvements and supplier qualification in a regulated manufacturing environment.
Listed on Beckman Coulter’s careers site · Apply there ↗
Principal Manufacturing Engineer - Implantable Device Unit
Biogen
Full-time · Cambridge, MA · $159,000 – $219,000
This role leads manufacturing strategy and execution for implantable drug delivery systems, working across development and commercialization phases to establish scalable processes and best practices. It suits an experienced medical device engineer who can influence cross-functional decisions, manage external partnerships, and drive innovation within strict regulatory frameworks.
Listed on Biogen’s careers site · Apply there ↗
A
Quality Assurance Specialist, Sr
A-dec
Newberg, OR
This role manages quality management systems and regulatory compliance for a medical device manufacturer, ensuring adherence to FDA and international standards through internal audits, corrective action programs, and cross-functional coordination. It suits someone with quality assurance experience in regulated industries who is comfortable with compliance documentation and comfortable leading others.
Listed on A-dec’s careers site · Apply there ↗
Sr Quality Engineer
Medtronic
3 locations
This role supports quality assurance in a regulated medical device manufacturing environment, managing investigations, compliance documentation, and continuous improvement across production processes. It suits engineers with healthcare manufacturing experience who are comfortable with FDA/ISO systems and can work cross-functionally to resolve quality issues.
Listed on Medtronic’s careers site · Apply there ↗
Choose a location to apply
Device Engineer III
Gilead Sciences
United States - California - Foster City · $117,895 – $152,570
This role supports the commercial lifecycle of combination drug-device products, handling design transfer, regulatory compliance, and post-launch engineering activities. It suits engineers with medical device manufacturing experience who want to work on established products rather than early-stage development.
Listed on Gilead Sciences’s careers site · Apply there ↗
Senior Quality Engineer (Sunday-Thursday)
Beckman Coulter
Full-time · Pensacola, FL
A quality engineering role overseeing membrane and medical device manufacturing operations at a life sciences company, ensuring regulatory compliance and driving continuous improvement across production. Suited for experienced quality engineers who want to lead complex problem-solving in a regulated, high-volume manufacturing environment.
Listed on Beckman Coulter’s careers site · Apply there ↗
Quality Technician III
Medtronic
Full-time · Mounds View, Minnesota, United States of America · $56,000 – $84,000
This role involves inspecting and testing returned medical devices as part of Medtronic's complaint handling process for cardiac ablation products, with responsibility for identifying failures and generating analysis reports. It suits someone with 3+ years of relevant experience who is comfortable working independently with technical equipment and documentation in a medical device environment.
Listed on Medtronic’s careers site · Apply there ↗
Associate Director, Quality Assurance Compliance
Gilead Sciences
Full-time · $165,495 – $235,620
This role leads quality assurance and regulatory inspection operations for a pharmaceutical manufacturing site, managing inspection readiness, compliance procedures, and digital quality systems. It suits experienced QA professionals in biotech or pharma who have managed regulatory agency interactions and can oversee complex inspection logistics across global operations.
Listed on Gilead Sciences’s careers site · Apply there ↗
Senior Plant Manager
Beckman Coulter
Full-time · Loveland, CO · $175,000 – $200,000
Lead manufacturing operations for a Colorado-based facility producing life sciences instruments and consumables, overseeing safety, quality, scheduling, and supply chain while driving continuous improvement across a large operations team. This role suits experienced operations leaders comfortable with complex, matrixed organizations who want to apply lean manufacturing expertise in a regulated, high-stakes industry.
Listed on Beckman Coulter’s careers site · Apply there ↗
Senior Quality Assurance Engineer
Beckman Coulter
Full-time · $116,000 – $159,500
This role develops quality systems and manages compliance for medical device manufacturing, ensuring products meet regulatory standards through design controls, risk assessment, and process validation. It suits experienced quality engineers who want to drive innovation in life sciences diagnostics while working on high-impact healthcare solutions.
Listed on Beckman Coulter’s careers site · Apply there ↗
Sr. Microbiology Quality Engineer
Beckman Coulter
Full-time · Hauppauge, NY · $112,000 – $125,000
This role leads complaint and defect tracking for medical device products in a regulated environment, working with cross-functional teams to resolve post-market quality issues and author investigation reports. It suits experienced microbiology professionals with a background in pharmaceutical or medical device quality assurance who want to take on broader leadership and strategic quality responsibilities.
Listed on Beckman Coulter’s careers site · Apply there ↗
Technical Project Manager, Global Operations (Reagent Assay/Hardware Development, NPI)
Beckman Coulter
Full-time · $135,000 – $145,000
This role manages multi-disciplinary projects and portfolios within Beckman Coulter's global operations, overseeing technology transfer and new product introduction initiatives for medical diagnostics hardware. The position suits experienced project managers with a background in manufacturing or medical device environments who can lead cross-functional teams through complex regulatory compliance requirements.
Sr. Manager, Quality Excellence
Beckman Coulter
Full-time · Hauppauge, NY · $155,000 – $175,000
This role leads quality management and regulatory compliance for a life sciences manufacturing site, overseeing quality assurance, control, and laboratory functions. It suits experienced quality professionals with deep knowledge of FDA regulations and ISO standards who want to drive operational excellence in a regulated biotech environment.
Listed on Beckman Coulter’s careers site · Apply there ↗