Bristol Myers Squibb
Upstream Senior Bioprocess Associate
Location: Devens, MA
Shift: Rotating 5am-5pm (eligible for 5% shift differential)
Overview Challenging, meaningful, and life‑changing work. In this role you’ll help optimize a production line and contribute to breakthroughs in cell therapy, transforming patients’ lives and your career. You’ll work on a variety of manufacturing tasks across the bioprocess chain and will be part of a high‑achieving team dedicated to continuous improvement.
Key Responsibilities
Execute routine manufacturing assignments per written procedures that are moderately complex with minimal instructions.
Adhere to Good Manufacturing Practices and standard operating procedures.
Weigh and check raw materials; assemble, clean, and sterilize process equipment; monitor processes.
Complete electronic work instructions and maintain a clean room environment to comply with regulatory requirements.
Operate primary production equipment (bioreactors, chromatography skids, media or buffer preparation equipment, etc.).
Use in‑process automation systems (Delta V, Syncade Interactions, Pi Vision) and supporting business systems (SAP, Infinity, Maximo, etc.) to maintain production records.
Revise and create process documents with little instruction; assist with process‑related investigations.
Help maintain material and components inventory level.
Review batch and exception reports for each manufacturing lot in collaboration with supervisor and Quality representative.
Assist with area‑specific initiatives related to work safety.
Qualifications & Experience
High school diploma required; knowledge of science (B.S. in science, engineering, biochemistry, or related discipline) desirable but not required.
Minimum 2+ years of process operations experience in a highly automated biotechnology manufacturing facility under GMP regulations.
Practical knowledge of GMP and company SOPs.
Evidence of successful participation on work teams requiring collaboration and results.
Proficiency with common computer tools: word processing, spreadsheet, and web‑based applications.
Prior experience where attention to detail and personal accountability were critical.
Good interpersonal skills; attentive and approachable.
Professional and productive relationship with area managers and co‑workers.
Compensation Overview Devens, MA – $26.44–$32.04 per hour (full‑time). Additional incentive cash and stock opportunities may be available. Final compensation based on demonstrated experience.
Benefits Medical, pharmacy, dental, and vision care; wellbeing programs; 401(k); short‑ and long‑term disability; life insurance; supplemental health insurance; travel protection; paid national and optional holidays; up to 120 hours of paid vacation; 2 paid days to volunteer; sick time; summer hours flexibility; parental, caregiver, and military leave; family care services; tuition reimbursement; recognition program; and more.
Equal Employment Opportunity & Accessibility BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws. BMS is dedicated to ensuring that people with disabilities can excel; reasonable workplace accommodations can be requested before accepting an offer by contacting adastaffingsupport@bms.com. For our full Equal Employment Opportunity statement visit careers.bms.com/eeo-accessibility.
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Overview Challenging, meaningful, and life‑changing work. In this role you’ll help optimize a production line and contribute to breakthroughs in cell therapy, transforming patients’ lives and your career. You’ll work on a variety of manufacturing tasks across the bioprocess chain and will be part of a high‑achieving team dedicated to continuous improvement.
Key Responsibilities
Execute routine manufacturing assignments per written procedures that are moderately complex with minimal instructions.
Adhere to Good Manufacturing Practices and standard operating procedures.
Weigh and check raw materials; assemble, clean, and sterilize process equipment; monitor processes.
Complete electronic work instructions and maintain a clean room environment to comply with regulatory requirements.
Operate primary production equipment (bioreactors, chromatography skids, media or buffer preparation equipment, etc.).
Use in‑process automation systems (Delta V, Syncade Interactions, Pi Vision) and supporting business systems (SAP, Infinity, Maximo, etc.) to maintain production records.
Revise and create process documents with little instruction; assist with process‑related investigations.
Help maintain material and components inventory level.
Review batch and exception reports for each manufacturing lot in collaboration with supervisor and Quality representative.
Assist with area‑specific initiatives related to work safety.
Qualifications & Experience
High school diploma required; knowledge of science (B.S. in science, engineering, biochemistry, or related discipline) desirable but not required.
Minimum 2+ years of process operations experience in a highly automated biotechnology manufacturing facility under GMP regulations.
Practical knowledge of GMP and company SOPs.
Evidence of successful participation on work teams requiring collaboration and results.
Proficiency with common computer tools: word processing, spreadsheet, and web‑based applications.
Prior experience where attention to detail and personal accountability were critical.
Good interpersonal skills; attentive and approachable.
Professional and productive relationship with area managers and co‑workers.
Compensation Overview Devens, MA – $26.44–$32.04 per hour (full‑time). Additional incentive cash and stock opportunities may be available. Final compensation based on demonstrated experience.
Benefits Medical, pharmacy, dental, and vision care; wellbeing programs; 401(k); short‑ and long‑term disability; life insurance; supplemental health insurance; travel protection; paid national and optional holidays; up to 120 hours of paid vacation; 2 paid days to volunteer; sick time; summer hours flexibility; parental, caregiver, and military leave; family care services; tuition reimbursement; recognition program; and more.
Equal Employment Opportunity & Accessibility BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws. BMS is dedicated to ensuring that people with disabilities can excel; reasonable workplace accommodations can be requested before accepting an offer by contacting adastaffingsupport@bms.com. For our full Equal Employment Opportunity statement visit careers.bms.com/eeo-accessibility.
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