Manufacturing Associate I
- Location
- San Diego, CA
- Listed
- 2 days ago
About the role
Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.
As a Manufacturing Associate I, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.
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.
Requirements
- 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.
Additional information
- This position follows an AWS/Panama 2-2-3 schedule, which is a rotating shift pattern designed to provide consistent coverage and extended time off.
- Schedule Details: 12-hour shifts
- Week 1: Work Monday & Tuesday, off Wednesday & Thursday, work Friday-Sunday
- Week 2: Off Monday & Tuesday, work Wednesday & Thursday, off Friday-Sunday
- This creates a repeating cycle of 2 days on, 2 days off, 3 days on, then the reverse the following week.
Why Capricor?
Capricor Therapeutics is advancing cell and exosome-based therapies with a focus on serious diseases where patients and families need new treatment options. Our work is grounded in scientific rigor, collaboration, and a shared commitment to moving meaningful therapies forward. Joining Capricor means being part of a mission-driven team working at the intersection of innovation, execution, and patient impact.
Come Work With Us
At Capricor, you’ll join a collaborative environment where employees are encouraged to contribute, grow, and help build the systems, science, and operations needed to support our next stage of growth. We value people who are thoughtful, accountable, hands-on, and motivated by work that can make a real difference.
Recruiting Fraud Notice
Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by someone using an official Capricor email address ending in @capricor.com. Capricor will never ask candidates to send money, deposit a check, purchase equipment, or provide payment for any reason as part of the recruiting or onboarding process.
Notice to Recruiting Agencies
Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without express written approval from Talent Acquisition and a fully executed agreement with Capricor. Agencies that contact hiring managers directly, solicit business, or submit candidates without prior approval will not be considered for engagement. Any unsolicited submissions will become the property of Capricor Therapeutics, and no fees will be paid for candidates hired as a result of such submissions. We appreciate your cooperation and respect for this policy.
From Capricor Therapeutics's careers page, first listed on Rolev.ai on November 7, 2026. Rolev.ai is not the employer.
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Common questions
Where is the Manufacturing Associate I job at Capricor Therapeutics located?
This Manufacturing Associate I position at Capricor Therapeutics is located in San Diego, CA. Always check Capricor Therapeutics's application page for specific state eligibility or relocation policies.
How do I apply for the Manufacturing Associate I position at Capricor Therapeutics?
This listing links directly to Capricor Therapeutics's Lever application page. You can apply directly on Capricor Therapeutics's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Lever application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.