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Associate II, Quality Assurance Shop Floor

Bristol Myers Squibb
Devens - MA, United States, United Statesfull_timeVerifiedPosted 26 Jan 2026
💰 $84,000/yr($70,000/yr$84,000/yr)

About the role

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Position Summary

The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Supply Chain Operations. 

This position will oversee and partner with operational areas, to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP. 

Shift: NIGHT shift available, Panama schedule (12-hour shift patterns with a 2-2-3 work cycle including weekends and holidays)

  • 6pm to 6am

Duties/Responsibilities

  • Provide Quality on-the-floor oversight to Manufacturing/ QC/ Supply Chain Operations & responding to minor issues or escalating to senior members. 

  • Perform and document operational verification per approved procedures. 

  • Observe manufacturing operations and identify departures from clean room behaviors and aseptic techniques.  

  • Provide quality oversight to maintenance operations and support pre-approved return to service plans. 

  • Perform area walkthroughs to identify quality issues and support remediation to ensure the floor and operations are in adherence with cGMP and approved procedures. 

  • Review manufacturing or testing records to ensure compliance with approved procedures. Communicate and resolve discrepancies and escalate as required.  

  • Identifies improvement opportunities and supports execution of site/team continuous improvement goals and projects.  

  • Maintain compliance with assigned learning plan. 

  • Support internal and external inspections as required.  

  • Contribute to the assessment of discrepancies and initiation of quality events. 

  • Participate in cross-department and cross-functional meetings, communicate in professional manner and share data/ knowledge within team.  

  • Build relationships within direct team and partner functions. 

Qualifications

Specific Knowledge, Skills, Abilities:

  • Ability to understand, follow, and apply approved procedures 

  • Possess basic computer skills with knowledge of MS Office 

  • Ability to understand problems and propose practical solutions 

  • Ability to communicate effectively with cross functional peers and direct management through written and verbal skills 

  • Ability to work in a fast-paced team environment with changing priorities. 

  • Detail oriented and task focused, with the ability to meet deadlines and prioritize assigned work. 

  • Ability to recognize the need for escalation of issues. 

  • Self-motivated and willingness to learn 

Education/Experience/ Licenses/Certifications:

  • Bachelor's degree in STEM field preferred. High school diploma/ Associates degree with equivalent combination of education and work experience may be considered. 

  • 0-2 years of relevant cGMP experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.  

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Devens - MA - US: $35.45 - $42.95per hour

The starting compensation range(s) for this role are listed a

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Company

Bristol Myers Squibb

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