Process Validation

Hims and Hers

Full-time · Menlo Park, CA · $130,000 – $155,000

This role leads the establishment and scaling of quality systems for a newly built peptide API manufacturing site with early-phase development capabilities. The ideal candidate is a hands-on quality leader who thrives in startup environments, can build practical GMP-compliant systems from the ground up, and works closely with operations and technical teams to ensure inspection readready manufacturing and development operations.

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

Beckman Coulter

Indianapolis, IN

This role involves overseeing the transition of reagent products from development to manufacturing and optimizing existing production processes at a life sciences company. It suits engineers with a regulated manufacturing background who want to bridge product development and operations in a diagnostics environment.

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 ↗

Medtronic

Full-time · Danvers, MA · $103,200 – $154,800

This Senior Process Engineer role focuses on developing and optimizing manufacturing processes for medical devices, with responsibility for driving automation, process validation, and cross-functional collaboration. The position suits experienced engineers with a background in regulated manufacturing who want to influence product scale-up and lead technical teams in a fast-paced healthcare environment.

Listed on Medtronic’s careers site · Apply there ↗

Merck

Full-time · Elkton, VA · $142,400 – $224,100

This role leads technical operations for a biopharmaceutical manufacturing site producing oral solid dose medications, overseeing process scale-up, technology transfer, and commercial production. It suits experienced pharmaceutical engineers and process specialists ready to manage manufacturing transitions from development to market while building team leadership capabilities.

Listed on Merck’s careers site · Apply there ↗

Moderna

Full-time · $109,200 – $174,600

This role oversees the transfer and optimization of Moderna's mRNA manufacturing processes to external contract manufacturers, ensuring quality and compliance across chemical and biologic production. It suits experienced pharmaceutical or biotech engineers with strong GMP expertise who thrive managing complex technical relationships and data-driven improvements across manufacturing networks.

Listed on Moderna’s careers site · Apply there ↗

Bristol Myers Squibb

Full-time · Indianapolis, IN · $124,449 – $150,803

This role leads validation and commissioning activities for a radiopharmaceutical manufacturing facility, ensuring GMP compliance as the operation transitions from construction to clinical and commercial production. It suits someone with deep manufacturing validation expertise who can independently manage complex programs while guiding a technical team through regulatory requirements and process improvements.

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

Gilead Sciences

United States - California - Foster City · $126,820 – $164,120

A technical leadership role designing and operating a new biologics manufacturing facility from the ground up, combining strategic facility design with hands-on floor execution. Ideal for experienced manufacturing professionals who want to architect cutting-edge single-use systems while directly managing their startup and ongoing operations.

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

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 ↗

Beckman Coulter

Full-time · West Sacramento, CA · $74,000 – $90,000

This is a manufacturing problem-solving role at a diagnostics company where you'd investigate production issues, lead corrective actions, and support pilot manufacturing for medical devices. It suits someone with a science degree and regulated manufacturing experience who can combine lab skills with quality troubleshooting.

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