Manufacturing Associate

Manufacturing Associate

Company: Bristol Myers Squibb |
Location: Summit West, NJ

Challenging. Meaningful. Life-changing. 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.

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.

Our Associates play a crucial role in supporting routine Cell Therapy manufacturing operations. We are looking for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs). Successful candidates must be goal-oriented and flexible, with the ability to work effectively on a team while demonstrating safety, quality, and GMP compliance at all times.

• Execute Cell Therapy Manufacturing operations in compliance with Source Governing Documents (SOPs, Work Instructions, Batch Records, Forms)
• Prioritize safety; report safety events within 24 hours and immediately escalate compliance issues
• Complete all documentation contemporaneously and in accordance with GMP requirements, including ALCOA+
• Execute the daily unit operations schedule across multiple shifts, including people, product, and material flow
• Perform aseptic processing and maintain cleanroom environmental conditions as required
• Complete training assignments on time and verify training completion prior to performing any GxP tasks
• Author and/or follow Manufacturing operating procedures in compliance with cGMP requirements
• Execute transactions in all electronic systems and adhere to business continuity processes

Education:

• Associate’s or Bachelor’s degree in a related field preferred; minimum high school diploma or equivalent required

Experience &

Skills:

• 0–1 years of cGMP cell therapy manufacturing, bioprocessing, or relevant experience
• Basic understanding of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing preferred
• Proficiency in common computer tools (word processing, spreadsheets, web-based applications)
• Meticulous attention to detail and strong personal accountability
• Excellent interpersonal skills; collaborative, attentive, and approachable

Working Conditions:

• Must be able to stand/walk for extended periods
• Must be able to work in a cleanroom environment performing aseptic processing in ISO 5 biosafety cabinets, with required PPE
• Must be able to lift/carry up to 30 lbs and push/pull up to 50 lbs multiple times per day
• Must be able to work in a BSL2 / ML1 environment handling human blood components and areas with vapor phase liquid nitrogen exposure
• Must be available to work assigned shifts including Days, Evenings, Nights, Weekends, and/or Holidays

Compensation: $27.83 – $33.72 per hour (Summit West, NJ). Additional incentive cash and stock opportunities may be available based on eligibility. Final individual compensation will be based on demonstrated experience.

Benefits include:

• Health Coverage: Medical, pharmacy, dental, and vision care
• Wellbeing Support: BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP)
• Financial Well-being & Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance
• Paid Time Off: Flexible time off (unlimited, with manager approval) and 11 paid national holidays for exempt employees; 160 hours annual paid vacation for hourly/non‑exempt employees plus 11 national holidays and 3 optional holidays
• Unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence, and an annual Global Shutdown between Christmas and New Year’s Day