Quality Control Associate II, Controls
Capricor
Job Summary 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. Responsibilities Generate, prepare, and maintain positive and negative control materials used in QC analytical assays. Support the qualification and characterization of control materials to ensure suitability for routine QC testing. Execute analytical assays to support control evaluation, assay troubleshooting, and assay optimization studies. Perform laboratory activities related to control generation, characterization, and assay performance evaluation. Maintain inventory, traceability, and documentation of assay control materials used across QC testing programs. Analyze experimental data, summarize results, and document findings in accordance with GMP and data integrity requirements. Document all laboratory work in GMP‑compliant systems including laboratory notebooks, controlled forms, and electronic records. Support preparation and maintenance of technical documentation including study protocols, reports, SOP updates, and control qualification records. Assist with investigations related to assay performance including deviations, OOS/OOT events, and atypical assay results. Collaborate with QC scientists and cross‑functional teams including Analytical Development, Process Development, Manufacturing, and Quality to support assay readiness and continuous improvement initiatives. Manage multiple laboratory assignments and testing priorities to meet project timelines and QC operational needs. Perform additional QC duties as assigned. Qualifications Bachelor’s degree in Biological Sciences, Biochemistry, Molecular Biology, or related discipline. 2+ years of laboratory experience in biotechnology, pharmaceutical, or GMP‑regulated environments. Hands‑on experience performing analytical assays such as ELISA, PCR/qPCR, flow cytometry, or other biochemical or cell‑based assays. Experience preparing or maintaining assay controls or reference materials. Strong laboratory documentation practices and familiarity with GMP and data integrity expectations. Ability to analyze data and communicate findings clearly. Ability to work independently and manage multiple assignments in a laboratory environment. Strong organizational and time‑management skills. Preferred Qualifications Experience supporting analytical studies related to assay performance or assay optimization. Experience working with mammalian cell culture or cell‑based assays. Experience supporting method qualification or assay performance monitoring activities. Experience supporting deviations, investigations, or technical reports in regulated environments. Experience working with cell therapy, biologics, or exosome‑based products. Laboratory‑based role requiring routine bench work. Work involves analytical instrumentation, laboratory documentation, and computer‑based data analysis. Ability to lift up to 20 pounds. Occasional participation in cross‑functional meetings and technical discussions. 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. #J-18808-Ljbffr
- ...pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most. The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in...Suggested
$75k - $87k
...Responsibilities Generate, prepare, and maintain positive and negative control materials used in QC analytical assays. Support the... ...Analytical Development, Process Development, Manufacturing, and Quality to support assay readiness and continuous improvement initiatives...Suggested$32 - $38 per hour
Quality Control Analyst II or III - Microbiology About this position OrganaBio was founded in 2018 with the mission to become the hub for tissue sourcing, clinical sample processing and contract manufacturing services to support cell and gene therapy developers around...SuggestedHourly payContract workMonday to FridayFlexible hours- ...and families who need them most. Position Summary The Quality Control Associate, Raw Materials is responsible for performing routine testing... ...laboratory or QC experience (academic or industry). ~ Associate II: 1+ years of QC experience in a regulated environment (...SuggestedWork at office
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BioLegend, Inc. is hiring a Quality Control Associate in San Diego, California. The role involves testing high-quality products such as antibodies and proteins while ensuring compliance with SOPs and ISO requirements. The ideal candidate should have lab experience and skills...- USLA BioLegend, Inc. is seeking a Quality Control Associate I for Flow Cytometry on the PM Shift in San Diego. The role involves testing high-quality reagents while following SOPs and ISO requirements. Candidates should be motivated science enthusiasts ready to work in...Shift work
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The Quality Control Associate III, Sample Management is responsible for the receipt, tracking, storage, distribution, and disposal of samples in a controlled laboratory or regulated environment. This role ensures sample integrity, accurate documentation, and compliance...$40 - $60 per hour
Abzena Inc. is looking for a Quality Control Associate I / II in San Diego, California. This role focuses on analytical testing and laboratory activities for biologics in a cGMP-regulated environment. The candidate will ensure compliance with regulatory requirements and...Hourly pay$83.5k - $133.5k
...results, and observations in laboratory notebooks and designated quality management systems in a clear, concise, and timely manner.... ...testing. Contribute to the continuous improvement of quality control processes and procedures. Adhere to all safety regulations and...- ...need them most. The QC Specialist, Analytical supports the quality and compliance of cell therapy programs through a focus on data... ...scientifically sound and fit for purpose. Contribute to change control activities and assess potential impact to product quality and...Work at officeShift work
$32 - $38 per hour
OrganaBio, based in San Diego, is seeking a Quality Control Analyst II or III for microbiology to perform QC testing and contamination control for cell therapy manufacturing. The successful candidate will execute environmental monitoring, microbiological assays, and ensure...Hourly pay- Performance Label International Inc in San Diego is seeking a Rewinder/Quality Control Assistant to join their dynamic team. This role is essential for ensuring high-quality products in an innovative environment. Candidates should have a strong attention to detail, basic...
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...results, and observations in laboratory notebooks and designated quality management systems in a clear, concise, and timely manner.... ...testing. Contribute to the continuous improvement of quality control processes and procedures. Adhere to all safety regulations and...- MillenniumSoft Inc is seeking a Quality System Specialist I in San Diego, CA. This role... ...with regulations, and managing document control processes. The ideal candidate will have... ...or GED, with a strong preference for an Associate's or Bachelor's Degree, and a minimum of...
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- Cooley LLP is seeking an IP US Filing Specialist (Quality Control) to join their IP Services team in San Diego. This role involves quality control functions for US patent filings and full support to patent attorneys, agents, and clients. The ideal candidate will have 3+...Work at office
- Capricor is seeking a Quality Control Associate, Raw Materials in San Diego, CA. The position involves ensuring that all raw materials comply with established specifications and regulatory requirements through hands-on laboratory work and documentation. The ideal candidate...
$23 - $35 per hour
...Quality Associate – San Diego Location: San Diego, CA Pay Rate: $23.00 - $35.00 per hour (based on experience) Shift: 2:30 PM - 11:00 PM (2... ...manufacturing environment 3+ years of experience in quality control, performing visual and mechanical inspections 3+ years of experience...Hourly payContract workFor contractorsLocal areaShift workAfternoon shift- ...patients and families who need them most. We are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling... ...deviation investigations, label issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate...Work at office
$75k - $85k
...with attention to detail who enjoys organizing, making processes better, and making a difference in patient lives. The Quality Assurance QA Associate II - Quality Events Team (QET) is responsible for cross‑functional triage of issues and managing, investigating, and...Work at officeRemote work$41.88 - $62.84 per hour
...Quality Assurance Inspector / Auditor OII OTECH is seeking a Quality Assurance Inspector / Auditor who will be required to comprehend... ..., procedures and equipment used meets applicable standards associated with unique undersea systems and supporting equipment. The...Hourly payFull time$24 - $45.5 per hour
...Quality Assurance Specialist (GMP) – Level I–III (DOE) We are seeking a detail-oriented Quality... ..., and finished products Perform document control activities, including SOPs, logbooks, and... ...environment: Level I: 2–4 years Level II: 3–5 years Level III: 5+ years Strong...Contract workTemporary work- OrganaBio, LLC is seeking a Quality Control Analyst II or III in San Diego, California. The successful candidate will perform quality control testing, assist with contamination control, and participate in training. This role requires a strong background in microbiology...
$32 - $38 per hour
OrganaBio, LLC in San Diego, California is seeking a Quality Control Analyst II or III in Microbiology. This role involves performing QC testing, assisting with contamination control, and adhering to cGMP regulations. The individual will execute microbiological assays...Hourly payMonday to Friday
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