Capricor Therapeutics
Facilities Associate II / III
San Diego, CA · Mid
Sponsorship not specified$75k-$95kDetected 78 days ago
ExpressRecruitingGMPCommunicationCollaborationOrganizational Skills
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.
- The ideal candidate brings hands-on GMP experience, demonstrates sound judgment in a regulated environment, and takes initiative in solving operational issues.
Responsibilities
- Own and manage the calibration and preventive maintenance program for GMP-critical equipment, ensuring accuracy, compliance, and timely execution.
- Lead the induction of new controlled assets into the inventory and maintenance tracking systems.
- Independently execute and improve daily, weekly, and monthly facilities operations to support manufacturing and laboratory readiness.
- Develop, revise, and optimize calibration and preventive maintenance schedules in alignment with operational needs and regulatory standards.
- Create and maintain accurate equipment documentation, including maintenance logs, procedures, and records.
- Drive vendor qualification processes in partnership with Quality Assurance, including documentation review and audit support.
- Collaborate with Quality Engineering to ensure timely completion and closure of equipment work orders, deviations, and change controls.
- Initiate and support quality records, including deviations, CAPAs, and change controls that impact GMP operations and facilities infrastructure.
- At the forefront of our innovation is Deramiocel ( CAP-1002 ), our lead cell therapy in late-stage development for Duchenne muscular dystrophy.
Requirements
- 3+ years of experience in a highly regulated facilities (GMP/ISO) or equipment maintenance role, ideally in biotech or pharmaceutical manufacturing.
- Strong understanding of GMP compliance, calibration standards, and equipment lifecycle management.
- Proficiency in equipment tracking and maintenance systems
- Must be able to sit and stand for extended periods.
- Must be able to lift/carry reports and materials up to 40 pounds, move about the office, communicate efficiently and effectively on the telephone or in person, and complete required paperwork.
Nice to have
- High school diploma or GED required.
- Bachelor's degree preferred, or equivalent relevant GMP experience in lieu of a degree
- experience with CMMS or QMS software a plus.
Compensation
- $75k-$95k
Company info
- We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology.
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This listing is sourced directly from Capricor Therapeutics's careers page and normalized into a canonical job model.