What are the responsibilities and job description for the Manufacturing Associate I position at Capricor Therapeutics, Inc.?
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 to ensure the highest standards
- Plan, collect, analyze, and report on production data, maintaining comprehensive records and observations
- Author, revise, and maintain SOPs through Capricor’s document change system
- Oversee inventory, material transfers, and cleanroom procedures to support efficient GMP operations
- Prepare technical summaries, protocols, and reports to ensure full documentation of production activities
- Lead moderate-complexity CAPAs and assist with deviations and investigations to maintain quality assurance
- Take on special projects in manufacturing and development as required
- 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, along with expertise in aseptic techniques
- Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries
- Strong organizational skills and acute attention to detail within a fast-paced, dynamic setting
- Basic molecular biology and flow cytometry skills are a plus
- Adaptability to work schedules that may include weekends or holidays as needed
Salary : $25 - $30