Bristolmyerssquibb
Manufacturing Associate, CAR-T
Summit West - NJ - US · Part-time
Sponsorship not specified$28k-$34kDetected 1 day ago
AccessibilityExcelClinical TrialsGMPFDA RegulatoryCell CultureCommunicationCollaborationWritingMicrosoft Office
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odds of building a lasting career here
15Unrated
Cap-exempt (no lottery)0
Sponsors this role0
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70
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About the role
- Additional incentive cash and stock opportunities (based on eligibility) may be available.
- Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment.
- Medical, pharmacy, dental, and vision care.
Responsibilities
- Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
- Support deviation investigations and write ups as needed. Support on time closure of any assigned CAPAs within the designated shift.
- Perform all tasks in a manner consistent with site safety policies, quality systems, and GMP requirements.
- Supervision will be managed by the shift Supervisor or designated Team Lead.
- Maintain on time completion of training assignments to maintain the necessary technical skills and process knowledge.
- Performs other tasks as assigned: continuous improvement projects, inspection readiness, right first-time initiatives, etc.
Requirements
- 0-1 years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience.
- however, ability to stand for extended periods of time may be necessary.
- Must be comfortable working with contained human blood components.
- Ability to lift 25 pounds.
- Must have the ability to work in laboratories and controlled, enclosed, restricted areas.
- Cleanroom garments and personal protective equipment will be required in designated areas which cover head, parts of the face, core body, and legs/feet.
- Aseptic technique is required for tube most activities: welding, connections, and transfers, at minimum.
- Aseptic qualification is required.
- Works in a team based, cross-functional environment to complete production tasks required by shift schedule.
Nice to have
- High School Diploma required.
- Bachelor's or associate degree preferred.
Skills
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique.
- Knowledge of cGMP/FDA regulated industry.
- Basic mathematical skills.
- General understanding of cGMPs.
- Technical writing capability.
- Proficient in MS Office applications.
- Background to include an understanding of biology, chemistry, medical or clinical practices
Compensation
- Compensation Overview:
Benefits
- Sufficient vision and hearing capability to work in job environment.
Company info
- At Bristol Myers Squibb we are reimagining the future of cell therapy.
- With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure.
- 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.
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