U.S.: Associate's or Bachelor's degree in a related field preferred; minimum high school diploma or equivalent required
Netherlands: MBO, level 3 or 4 in a science-related field or equivalent
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
Ability to maintain professional relationships with management and co-workers
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 (safety shoes, glasses, aprons, face shields, PAPR, lab coats, full body gowns, hairnets, gloves, and hearing protection)
Must be able to lift/carry up to 30 lbs / 15 kg and push/pull up to 50 lbs / 25 kg 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
This job description describes the general nature of the role. Additional duties may be assigned as needed by management.
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:
Summit West - NJ - US: $27.83 - $33.72per hour
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial
Benefits
Health insuranceDental insuranceVision insuranceFlexible scheduleEquity / stock options
Additional Information
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
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.
Duties & Responsibilities
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
Bristol-myers Squibb · Summit West, NJ