More jobs:
Manufacturing Associate
Job in
Bend, Deschutes County, Oregon, 97707, USA
Listed on 2026-07-21
Listing for:
Bristol-Myers Squibb
Full Time
position Listed on 2026-07-21
Job specializations:
-
Manufacturing / Production
Manufacturing & Industrial Operations, Production Associate / Production Line, Production QC/QA, Quality Engineering
Job Description & How to Apply Below
Overview
Join Bristol Myers Squibb as a Manufacturing Associate, Cell Therapy. Work in a cGMP cleanroom environment to manufacture human blood-derived components per Batch Record and Standard Operating Procedures under supervision. The role supports production, deviation investigations, and quality investigations within a team-based schedule.
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 assigned CAPAs within the designated shift.
- Adhere to aseptic technique for tube-related activities (welding, connections, transfers) and maintain aseptic qualification.
- Weigh and measure in-process materials to ensure proper quantities are added/removed.
- Adhere to production schedule to ensure on-time internal production logistics.
- Record production data in a clear, concise format according to GDPs.
- Perform tasks in alignment with site safety policies, quality systems, and GMP requirements.
- Work in a cross-functional, team-based environment to complete shift-based production tasks.
- Develop expertise within designated function and pursue training to become a SME and qualified trainer; maintain on-time completion of training assignments.
- Perform other tasks as assigned (e.g., continuous improvement projects, inspection readiness, right-first-time initiatives).
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab techniques.
- Knowledge of cGMP/FDA regulated industry.
- Basic mathematical skills and general understanding of cGMPs.
- Technical writing capability.
- Proficiency in MS Office applications.
- High School Diploma required;
Bachelor’s or associate degree preferred. - 0-1 years of cGMP cell therapy manufacturing or bioprocessing experience.
- Intermittent walking, standing, and sitting; ability to stand for extended periods may be necessary.
- Comfortable working with contained human blood components; ability to lift up to 25 pounds.
- Work in laboratories and controlled, enclosed, restricted areas with cleanroom garments and PPE as required.
- Restricted areas prohibit food and outside materials; PPE must be worn in designated areas.
- Clean room environment with specific pressure and temperature controls; routine exposure to sanitization agents and human blood components.
- Compensation:
Summit West, NJ, US: $27.83 - $33.72 per hour; additional incentive cash and stock opportunities may be available. - Benefits include health coverage, wellbeing programs, 401(k), disability and life insurance, and paid time off; eligibility may vary by job and location.
- On-site protocol and disability accommodations information available; visit the company site for Equal Employment Opportunity statements and data privacy information.
For more information about working at BMS, refer to official careers pages. This description preserves the essential duties, qualifications, and expectations of the role without altering its context.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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