Interested in a challenging and rewarding career where you can make a difference?

Then Bristol-Myers Squibb is the place for you.

Ignite your inner passion and achieve your greatest potential
by joining Bristol-Myers Squibb.

We are a team dedicated to discovering, developing and delivering innovative medicines
that help patients prevail over serious diseases. Our commitment is to foster a globally
diverse and inclusive workforce with a high-performing culture that is agile,
entrepreneurial and accountable. This enables our business strategy while
encouraging excellence, growth, achievement, innovation and a balance between our
personal and professional lives.

By combining the reach and resources of a global pharmaceutical company with the can-do spirit and agility of a biotechnology company, we are becoming a leader for the future – a next-generation BioPharma leader.

Our vision requires bold leaders. People like you.

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Recent Job Openings

Senior Validation Engineer - Mount Vernon, IN
Description: Supports validation lifecycle for systems including, but not limited to, cleaning and/or process validation.  Supports validation lifecycle for new and existing systems including, but not limited to, cleaning and/or process validation.  Support process and packaging cleaning validation projects from concept and development through full execution of protocol with focus on quality, robust, and efficient processes.  Suppo...
Reference Code: 24168
TPM QA MGR BIOLOGICS - New Brunswick, NJ
Description: Monitor the quality operations and compliance activities of a third party manufacturer of BMS drug substance and drug products. Perform product disposition activities which are aligned with BMS operations functions to ensure the timely supply of drug substance meet clinical and commercial customer requirements while ensuring compliance with testing standards, SOPs, validation guidelines and regulatory filings. Review and...
Reference Code: 24215
Quality Engineer - Devens, MA
Description: 1.Primary responsibility is to ensure that all biotechnology validationdocumentation meets external regulatory and internal WWQC guidelines and requirements. 2.Provide document review and approval for Process, Equipment, Computer and Analytical Validation commissioning and qualification documentation from both technical and compliance perspectives. 3.Act as champion for and participate in local and global change control...
Reference Code: 24142