Biotech GMP Manufacturing Associate I — Cell Culture

Capricor Therapeutics, Inc.

San Diego (CA)

On-site

USD 65,000 - 90,000

Full time

11 hours ago
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Benefits offered by this job

Medical, dental, vision coverage
401(k) with company match
Paid time off and holidays

Job summary

Capricor Therapeutics is seeking a Manufacturing Associate I to join a GMP-compliant team in a cGMP cleanroom environment. You will perform routine cell culture and manufacturing tasks while ensuring precise documentation and data integrity across batch records and SOPs.

The role supports critical clinical trials and exosome development, with a rotating 12-hour schedule and potential weekend work. Capricor offers a competitive benefits package and growth opportunities.

Qualifications

  • 1-3 years of experience in a cGMP/cGTP manufacturing environment.
  • Experience with mammalian tissue culture and aseptic techniques.
  • Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries.
  • Strong organizational skills and acute attention to detail in a fast-paced setting.
  • Basic molecular biology and flow cytometry skills are a plus.
  • Adaptability to weekend/holiday schedules as needed.

Responsibilities

  • Perform routine manufacturing tasks including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing.
  • Complete and ensure timely, accurate GMP documentation across batch records, forms, and protocols.
  • Mentor fellow team members on cGMP documentation protocols.
  • Plan, collect, analyze, and report on production data with comprehensive records.
  • Author, revise, and maintain SOPs in Capricor’s document system.
  • Oversee inventory, material transfers, and cleanroom procedures.
  • Prepare technical summaries, protocols, and reports of production activities.
  • Lead moderate-complexity CAPAs and assist with deviations and investigations.
  • Take on special projects in manufacturing and development as required.

Skills

cGMP knowledge
Cell culture
Documentation
Regulatory awareness
Attention to detail

Tools

Flow cytometry
Molecular biology basics

Job description

Capricor Therapeutics is seeking a Manufacturing Associate I to join a GMP-compliant team in a cGMP cleanroom environment. You will perform routine cell culture and manufacturing tasks while ensuring precise documentation and data integrity across batch records and SOPs.

The role supports critical clinical trials and exosome development, with a rotating 12-hour schedule and potential weekend work. Capricor offers a competitive benefits package and growth opportunities.

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