Capricor Therapeutics, Inc.
Capricor Therapeutics, Inc. is advancing cell and exosome‑based therapies for rare diseases. Our lead product, Deramiocel (CAP‑1002), is in late‑stage development for Duchenne muscular dystrophy. We also use the StealthX™ exosome platform for targeted delivery and vaccinology.
Base pay range $55,000.00/yr – $75,000.00/yr
GMP Operations Associate I – Facilities Coordinator This role ensures operational excellence and compliance in Capricor’s GMP environment. Responsibilities include managing equipment calibration, preventing maintenance schedules, coordinating vendor activities, and supporting facilities operations to uphold quality and regulatory standards.
Responsibilities
Maintain and update calibration and preventive maintenance (PM) schedules for GMP‑controlled equipment.
Support induction and documentation of controlled assets in compliance with requirements.
Coordinate daily, weekly, and monthly facilities tasks to ensure uninterrupted operations.
Schedule PM and calibration activities with external vendors and collaborate with internal teams to minimize operational impact.
Partner with Quality Assurance (QA) on vendor qualification and compliance verification.
Work closely with Quality Engineering to ensure timely completion and closure of equipment‑related work orders.
Communicate with vendors for troubleshooting and repair needs, ensuring swift resolution.
Assist in managing quality records, including deviations, CAPAs, and change controls related to GMP operations and facilities.
Contribute to the revision and upkeep of equipment documentation and SOPs.
Ensure all activities adhere to GMP regulations, internal policies, and industry best practices.
Requirements
Bachelor’s degree in Engineering, Life Sciences, or a related field preferred; equivalent experience considered.
Familiarity with GMP regulations and standards governing equipment and facilities operations.
Basic understanding of calibration and maintenance processes for controlled equipment.
Strong organizational and time‑management skills with the ability to prioritize multiple tasks.
Excellent communication and coordination skills for effective vendor and team interactions.
Ability to work independently while maintaining a collaborative approach.
Detail‑oriented with strong problem‑solving capabilities.
Experience with quality management systems or documentation processes is a plus.
Comfortable operating in a fast‑paced, highly regulated environment.
Why Capricor? Capricor Therapeutics is redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient‑centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission‑driven group that’s transforming lives with every breakthrough.
Come Work With Us! At Capricor, you’ll thrive in a collaborative environment that nurtures professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through cutting‑edge therapies.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
#J-18808-Ljbffr
Base pay range $55,000.00/yr – $75,000.00/yr
GMP Operations Associate I – Facilities Coordinator This role ensures operational excellence and compliance in Capricor’s GMP environment. Responsibilities include managing equipment calibration, preventing maintenance schedules, coordinating vendor activities, and supporting facilities operations to uphold quality and regulatory standards.
Responsibilities
Maintain and update calibration and preventive maintenance (PM) schedules for GMP‑controlled equipment.
Support induction and documentation of controlled assets in compliance with requirements.
Coordinate daily, weekly, and monthly facilities tasks to ensure uninterrupted operations.
Schedule PM and calibration activities with external vendors and collaborate with internal teams to minimize operational impact.
Partner with Quality Assurance (QA) on vendor qualification and compliance verification.
Work closely with Quality Engineering to ensure timely completion and closure of equipment‑related work orders.
Communicate with vendors for troubleshooting and repair needs, ensuring swift resolution.
Assist in managing quality records, including deviations, CAPAs, and change controls related to GMP operations and facilities.
Contribute to the revision and upkeep of equipment documentation and SOPs.
Ensure all activities adhere to GMP regulations, internal policies, and industry best practices.
Requirements
Bachelor’s degree in Engineering, Life Sciences, or a related field preferred; equivalent experience considered.
Familiarity with GMP regulations and standards governing equipment and facilities operations.
Basic understanding of calibration and maintenance processes for controlled equipment.
Strong organizational and time‑management skills with the ability to prioritize multiple tasks.
Excellent communication and coordination skills for effective vendor and team interactions.
Ability to work independently while maintaining a collaborative approach.
Detail‑oriented with strong problem‑solving capabilities.
Experience with quality management systems or documentation processes is a plus.
Comfortable operating in a fast‑paced, highly regulated environment.
Why Capricor? Capricor Therapeutics is redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient‑centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission‑driven group that’s transforming lives with every breakthrough.
Come Work With Us! At Capricor, you’ll thrive in a collaborative environment that nurtures professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through cutting‑edge therapies.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
#J-18808-Ljbffr