Bristol Myers Squibb
Senior Bioprocess Associate
Devens - MA - US, USA · Senior · Full-time
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About the role
- The starting pay range(s) listed above is for full-time employees (FTE).
- You may also be eligible for additional discretionary incentive cash and stock opportunities.
- The Senior Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease.
Responsibilities
- Revise and create process documents and assist with process related investigations
- Lead in maintaining material and components inventory level
- Support a safe work environment and contribute to area specific initiatives associated with work safety
- Completes work instructions and maintains a clean room environment to comply with regulatory requirements.
- Effectively uses in process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo, etc.) to maintain production records.
- Assist in revising and creating process documents (i.e., SOPs and Batch Records) and assist with process-related investigations.
- Maintains a professional and productive relationship with area management and co-workers.
- BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.
Requirements
- If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.com with the Job Title and Requisition number.
- Works on routine manufacturing assignments per written procedures that are moderately complex with minimal instructions, where the ability to recognize deviation from accepted practice is required.
- Train for proficiency in process automation and supporting business systems and in the operation of primary production equipment within the assigned functional area.
- High school diploma is required.
- Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry or related discipline, or its equivalent is desired but not required.
- Demonstrated proficiency in common computer tools such as word processing, spreadsheet, and web-based applications.
Compensation
- The starting pay range(s) listed above is for full-time employees (FTE).
- Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.
Benefits
- U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.
- Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.
- U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits
- Final compensation is guided by pay equity principles and applicable employment laws.
Company info
- If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com.
- Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.
Equal opportunity
- Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.
- Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
This listing is sourced directly from Bristol Myers Squibb's careers page and normalized into a canonical job model.