Bristol Myers Squibb
The Validation Engineer I supports the Radiopharmaceutical facility and GMP operations by assisting with the drafting and execution of commissioning, qualification, and validation documents. Working under senior guidance, the role contributes to validation activities that support the transition from construction to clinical development and ongoing commercial operations. Additional duties include supporting new technology onboarding, deviation investigations, and facility expansion projects.
Headquarters
Lawrence Township, New Jersey, United States
Company Size
10001+ employees
Founded
1887
Bristol Myers Squibb is a global biopharmaceutical company that discovers, develops, and delivers prescription medicines for serious diseases, with a focus on oncology, hematology, immunology, cardiovascular, neuroscience, and other therapeutic areas. The company operates in the pharmaceutical and biotechnology industry, serving patients worldwide through research, development, manufacturing, and commercialization of innovative therapies.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Bristol Myers Squibb.
21% above the average for this role
Sr. Engineer, Commissioning, Qualification, and Validation
Moderna
Validation Engineer
Syner-G
Intern - Validation Engineering
Roche
Sr. Commissioning, Qualification and Validation (CQV) Engineer
VTI Life Sciences
Senior Validation Engineer, CQV Sterility Assurance
RayzeBio
Validation Engineer II
Civica Infrastructure