4 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
Senior Supplier Quality Engineer
Medtronic
Full-time · 2 locations · $99,200 – $148,800
This role manages supplier quality and component qualification for new cardiac surgery devices at Medtronic, working across engineering, regulatory, and sourcing teams to ensure devices meet quality and regulatory standards. It suits someone with medical device manufacturing experience who can lead supplier audits, resolve quality issues, and coordinate development activities within tight program timelines.
Listed on Medtronic’s careers site · Apply there ↗
Choose a location to apply
Executive Director, Program and Study Management, Infectious Diseases and Vaccines
Merck
Full-time · $255,800 – $402,700
This executive role oversees clinical trial operations and program management for infectious disease and vaccine programs at a major pharmaceutical company, with accountability for strategy, delivery, budgets exceeding $1B, and leadership of approximately 500 staff across multiple countries. It suits an experienced clinical development leader with strong regulatory knowledge, executive presence, and proven ability to modernize operations through digital and AI-enabled solutions.
Clinical TrialsRegulatory RequirementsStrategic LeadershipArtificial IntelligenceGood Clinical Practice
Listed on Merck’s careers site · Apply there ↗
Director, Medical Safety Assessment Physician
Bristol Myers Squibb
Full-time · $255,860 – $310,040
Lead medical safety strategy and oversight for assigned pharmaceutical compounds across development and postmarketing phases, managing benefit-risk evaluations and regulatory submissions. Suited for physicians with pharmacovigilance experience who want to direct patient safety strategy at a major pharmaceutical company.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Distinguished Scientist, Clinical Research, Thoracic Malignancies
Merck
Full-time · $310,900 – $489,400
This senior pharmaceutical leadership role oversees the full lifecycle of clinical trials for thoracic cancer drugs, from early development through regulatory approval and publication. It suits an MD or MD/PhD with deep oncology expertise who has managed drug development in industry and can lead cross-functional teams while maintaining current scientific knowledge in their field.
Listed on Merck’s careers site · Apply there ↗