Manufacturing Associate I
Capricor Therapeutics, Inc.
June 25, 2026
On-site
San Diego, CA
$25 - $30 USD yearly
Operations
Responsibilities:
- Perform routine manufacturing tasks, including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing
- Complete and ensure timely, accurate documentation in compliance with GMP standards across batch records, forms, and protocols
- Mentor fellow team members on cGMP documentation protocols
- Plan, collect, analyze, and report on production data, maintaining comprehensive records and observations
- Author, revise, and maintain SOPs through the document change system
- Oversee inventory, material transfers, and cleanroom procedures to support efficient GMP operations
- Prepare technical summaries, protocols, and reports to fully document production activities
- Lead moderate-complexity CAPAs and assist with deviations and investigations
- Take on special projects in manufacturing and development as required
Requirements:
- Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field
- 1–3 years of experience in a cGMP/cGTP manufacturing environment
- Solid laboratory experience in mammalian tissue culture and expertise in aseptic techniques
- Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries
- Strong organizational skills and attention to detail in a fast-paced environment
- Basic molecular biology and flow cytometry skills (plus)
- Ability to work schedules that may include weekends or holidays as needed
Benefits:
- Employer-sponsored medical, dental, and vision coverage; company-paid basic life and AD&D insurance; 401(k) plan with company match; paid time off and company holidays; paid parental leave; additional voluntary benefits and wellness programs (if available).
- Perform routine manufacturing tasks, including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing
- Complete and ensure timely, accurate documentation in compliance with GMP standards across batch records, forms, and protocols
- Mentor fellow team members on cGMP documentation protocols
- Plan, collect, analyze, and report on production data, maintaining comprehensive records and observations
- Author, revise, and maintain SOPs through the document change system
- Oversee inventory, material transfers, and cleanroom procedures to support efficient GMP operations
- Prepare technical summaries, protocols, and reports to fully document production activities
- Lead moderate-complexity CAPAs and assist with deviations and investigations
- Take on special projects in manufacturing and development as required
Requirements:
- Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field
- 1–3 years of experience in a cGMP/cGTP manufacturing environment
- Solid laboratory experience in mammalian tissue culture and expertise in aseptic techniques
- Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries
- Strong organizational skills and attention to detail in a fast-paced environment
- Basic molecular biology and flow cytometry skills (plus)
- Ability to work schedules that may include weekends or holidays as needed
Benefits:
- Employer-sponsored medical, dental, and vision coverage; company-paid basic life and AD&D insurance; 401(k) plan with company match; paid time off and company holidays; paid parental leave; additional voluntary benefits and wellness programs (if available).