Not specified; not specified; competitive benefits...
Hybrid (50% onsite)
8-10+ years pharmaceutical industry experience
In-depth knowledge of cgmp and gdp regulations
Direct experience with external manufacturers cmos
Bristol Myers Squibb is seeking a Senior Manager of Quality Compliance for External Manufacturing on a 12-month fixed-term contract. The role involves ensuring compliance with quality standards and regulations in pharmaceutical and biologics external manufacturing while providing oversight and support for quality operations
Job Summary
The Senior Manager provides quality compliance oversight for pharma and biologics CMOs within the Global External Manufacturing network.
Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs to support employee goals at work and in personal lives.
This role requires serving as the subject matter expert for audits, inspections, and regulatory alignment across international markets.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking a Senior Manager of Quality Compliance for External Manufacturing on a 12-month fixed-term contract. The role involves ensuring compliance with quality standards and regulations in pharmaceutical and biologics external manufacturing while providing oversight and support for quality operations.
Salary
Not specified; Not specified; Competitive benefits and programs offered
Skills & Requirements
Must-have
8-10+ years pharmaceutical industry experience
In-depth knowledge of cGMP and GDP regulations
Direct experience with external manufacturers CMOs
Experience leading Health Authority inspections
Expertise in Quality Systems Change Control CAPA
Nice-to-have
Strong negotiation and interpersonal skills
Ability to lead geographically dispersed teams
Experience with biologics manufacturing operations
Proactive continuous improvement mindset
Confidence in public speaking and presentations
Key Requirements
BSc or equivalent in Natural Sciences, Chemistry, Microbiology, Biology, or Pharmacy
8-10+ years' experience in pharmaceutical Quality, Manufacturing Technology, or Regulatory Affairs
Direct experience interacting with FDA, EMA, and other Health Authorities