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Biomedical Assistant - GMP Manufacturing
Company: Cedars-Sinai
Location: West Hollywood, CA
Employment Type: Full Time
Date Posted: 08/10/2026
Job Categories: Biotechnology and Pharmaceutical, Engineering, Finance/Economics, Healthcare, Other, Healthcare, Practitioner and Technician, Human Resources, Information Technology, Manufacturing and Production, Science, Counseling, Executive Management, Medical
Job Description
Biomedical Assistant - GMP Manufacturing

Job Description

With your help, we can change the future of healthcare!

The Cedars-Sinai Biomanufacturing Center (CBC) is a state-of-the art facility that comprises of a cGMP cell manufacturing facility housing multiple cleanroom cell production suites and process development rooms for producing the next generation of cell and gene therapies. With world class expertise in stem cell (iPSC) biology, bioprocessing, translational, regulatory and manufacturing, Cedars-Sinai is committed to pushing the frontiers of medicine and discovering new technologies and innovations that will impact how we diagnose and treat disease. To learn more about the CBC, please visit Home - CSBIO (csbiomfg.com).

Are you ready to be a part of groundbreaking research?

The Biomedical Assistant performs activities associated with the maintenance of controlled areas or shared lab resources in accordance with company policies and procedures. May perform laboratory tests, assist with lab work and experiments, and conduct analysis under supervision of manager, and/or scientist. Follows standard operating procedures (SOPs). Ensures all laboratory equipment and work areas are clean, sterile, and in proper working order. May be responsible for calibration of instruments. Performs general tasks and completes routine assignments. Receives assistance in the completion of more complex assignments.

Primary Duties and Responsibilities:

  • Prepares sterile and non-sterile stock and working solutions.
  • Cleans and maintains laboratory area(s), equipment and glassware.
  • Supports occasionally experimentation and production activities as directed.
  • Documents information by maintaining daily logs, equipment record books and/or computer database(s). Drafts standard operating procedures.
  • Maintains daily lab equipment operations by following operating instructions, troubleshooting breakdowns, maintaining supplies, performing preventive maintenance and calling for repairs, as needed.
  • Administers laboratory supplies ready by inventorying stock, placing orders and verifying receipt.

Qualifications

Education:

  • High School Diploma/GED, required.

Experience and Skills:

  • One (1) year of experience in a lab or biotech setting.
  • Knowledge of regulatory requirements including Federal, FDA, State, GLP, and accrediting agency requirements.
  • Ability to record log samples, test results from experiments, and project records.
  • Ability to help scientists with handing instruments and materials with knowledge of equipment or assist in performing tasks in the lab.
  • Ability to multi-task in a high impact and demanding environment.
  • Understanding of general research objectives.
  • Working knowledge of database management, personal computers, and presentation and imaging software.
  • Understanding of general research objectives. Familiar with routine laboratory procedures and experimental protocols.
  • Must possess computer skills to include, but not limited to, Excel and Word.
Contact Information
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