Capricor Therapeutics
Manufacturing Supervisor
San Diego, CA
Sponsorship not specified$100k-$118kDetected 41 days ago
Data AnalysisComplianceProcess ImprovementInventory ManagementRecruitingGMPCell CultureLeadershipCommunicationCollaborationProblem SolvingMentoringPublic Speaking
About the role
- Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases.
- 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 Supervisor, you will oversee the manufacturing team, ensuring cGMP-compliant production of biologic products for clinical trials.
Responsibilities
- Supervise the manufacturing team, including Technicians, Associates (I-II, III, III-Lead), to ensure seamless execution of production tasks such as cell culture, media preparation, formulation, centrifugation, and freezing.
- Coordinate with the Associate Director of Manufacturing to develop production schedules, allocate resources, and address operational challenges.
- Lead training and mentoring of manufacturing staff, ensuring team competency in aseptic techniques, cGMP standards, and manufacturing procedures.
- Author, review, and update standard operating procedures (SOPs) and other manufacturing documentation using the document change system.
- Manage inventory, material transfers, and cleanroom setup/shutdown activities to support continuous manufacturing operations.
- Lead special manufacturing and development projects as assigned by the Associate Director of Manufacturing.
- Perform other duties as assigned to support manufacturing operations and company goals.
- At the forefront of our innovation is Deramiocel ( CAP-1002 ), our lead cell therapy in late-stage development for Duchenne muscular dystrophy.
- You will supervise daily operations, mentor staff, and collaborate with the Associate Director of Manufacturing to drive efficiency, quality, and regulatory adherence.
Requirements
- 6+ years of experience in a cGMP manufacturing environment, with at least 2-3 years in a supervisory or leadership role.
- In-depth knowledge of cell culture, aseptic techniques, cGMP standards, and regulatory compliance in a biotech/pharma setting.
- Proven expertise in Good Documentation Practices (GDP) and managing manufacturing documentation.
- Experience leading deviation investigations, CAPAs, and process improvement initiatives.
- Proficiency in data analysis, technical report writing, and presenting production metrics.
- Ability to gown and work in classified cleanroom areas, ensuring compliance with ISO 7 standards.
- Primarily cleanroom-based with required time in GMP spaces overseeing manufacturing operations and team activities.
- Ability to navigate cleanroom and GMP environments for production oversight and staff training.
Nice to have
- advanced degree preferred.
- Bachelor's degree in Biological Sciences, Biomedical Engineering, or related field
Compensation
- $100k-$118k
Company info
- We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology.
Apply directly at Capricor Therapeutics →Create a free account for alerts like thisView Capricor Therapeutics immigration profile
This listing is sourced directly from Capricor Therapeutics's careers page and normalized into a canonical job model.