Bristol Myers Squibb
Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations
Summit West - NJ - US · Part-time
Sponsorship not specified$28k-$34kDetected 5 days ago
AccessibilityExcelClinical TrialsGMPFDA RegulatoryCell CultureCommunicationCollaborationWritingMicrosoft Office
About the role
- 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.
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.
- Become a SME and qualified trainer within a designated function of manufacturing. 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
- Intermittent walking, standing and sitting to perform job functions; however, ability to stand for extended periods of time may be necessary.
Requirements
- 0-1 years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience.
- If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team.
- Communication of production deviations and assistance with quality investigations are required, as applicable.
- 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.
- Must be comfortable working with contained human blood components.
- 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.
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
- 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
- Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Benefits
- Sufficient vision and hearing capability to work in job environment.
- Medical, pharmacy, dental, and vision care.
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This listing is sourced directly from Bristol Myers Squibb's careers page and normalized into a canonical job model.