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
$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$75k - $87k
...A biotechnology company in San Diego is seeking a laboratory professional to support quality control (QC) analytical assays. The ideal candidate will have a Bachelor's in Biological Sciences and at least 2 years of experience in laboratory environments. Responsibilities...Suggested$85k - $89k
...Quality Assurance Specialist II – San Diego By Catalent, Inc., a leading global contract development and manufacturing organization (CDMO), this... ...update documents related to material management quality control, batch records, compliance, and validation systems. Participate...SuggestedContract work$20.77 - $30.77 per hour
...brands include Friction Technologies, KONI and Axtone. Connect and Control Technologies: A leader in critical applications for the... ...various stages of the production process to ensure adherence to quality standards and specifications. You will identify defect, deviations...SuggestedHourly payTemporary workWork at office$83.5k - $133.5k
...results, and observations in laboratory notebooks and designated quality management systems in a clear, concise, and timely manner.... ...microbiological testing. Contribute to the continuous improvement of quality control processes and procedures. Adhere to all safety regulations and...Suggested$83.5k - $133.5k
...laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive... ...testing. Contribute to the continuous improvement of quality control processes and procedures. Adhere to all safety regulations and...Full timeWorldwide- ...A biotech company in San Diego seeks an Entry Level Quality Control Associate I. Responsibilities include accurate testing of QC samples, data analysis, and documentation following standard protocols. Ideal candidates will possess a BA/BS in a scientific discipline and...Full timeContract work
$76.44k - $159.43k
...Description Develop, implement, and maintain the project‑specific Quality Assurance Surveillance Plan (QASP) in compliance with Federal... ...required standards. Oversee construction contractor’s Quality Control meetings (Preparatory, Initial, and Follow‑Up) with project stakeholders...Contract workFor contractorsFor subcontractorH1bFlexible hours$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- ...Capricor Therapeutics in San Diego is hiring a Quality Control Associate, Raw Materials. This role involves routine testing of raw materials, ensuring compliance with quality and safety standards. Candidates should have a Bachelor's degree in a related field and some laboratory...
- ...Therapeutics in San Diego seeks a QC Analyst to generate and manage QC control materials, perform analytical assays (ELISA, PCR/qPCR, flow... ...Development, Process Development, Manufacturing, and Quality to ensure assay readiness and quality control efficiency. The role...
- ...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...Work at office
- Grifols Diagnostic Solutions in San Diego is seeking a QC Support Analyst 4 to test and release raw materials, sub-assemblies or finished goods within GMP/GLP practices. To succeed you should have a BA/BS in Biological Science or Chemistry with 2–4 years of QC experience...
$60k - $70k
...LifeSciences is seeking a #MiracleMaker to join our Quality Assurance team as a QA Operations Specialist II. The QA Operations Specialist II is responsible for... ..., NCRs, CAPAs, supplier management, change controls, and controlled documentation management, etc. Provides...For contractorsWork at officeLocal areaWork from home- ...of Design History Records, Device Master Records, Nonconformances, Document Changes, Validations and Change Controls Demonstrates working knowledge of Quality Control, Manufacturing and Inventory processes Leads internal, external & 3rd party audits Reviews Customer Notifications...
$90k - $125k
...quickly and safely. We are dedicated to quality excellence. We are driven to get better... ...contact for Batch Disposition, Quality Control and Quality Record escalations and document... ...and ensure development of respective associates. $90,000 - $125,000 a year FLSA: Exempt...Work at officeLocal area$100k - $118k
...supporting off-hours GMP manufacturing. As a Quality Assurance Specialist at Capricor, you... ...quality records, logbooks, forms, and associated documentation as authorized. Identify, document... .... Support investigations, CAPAs, change controls, and quality risk assessments as...Shift workNight shift- ...continuous improvement and operational excellence across the organization. You will be the primary contact for Batch Disposition, Quality Control and Quality Records, collaborating with PMO and other departments to ensure timely, compliant deliverables. This role...
$135.43k - $178.48k
...Clinical Laboratory Scientist Specialist with primary responsible for quality system oversight for rapid response laboratory and transfusion... ...BPDR/regulatory assessments; support validation/change control and PDSA/process improvement activities; and collaborates with...Hourly payDay shift- ...Maravai LifeSciences is seeking a QA Operations Specialist II to maintain and improve the Quality Management System. You will review deviations, NCRs, CAPAs, supplier management, change controls, and documentation, ensuring compliance with domestic and international standards...
- ...Hanna Interpreting Services LLC is seeking a Warranty Claims & Quality Control Specialist in San Diego, California. This role involves managing workflows for on-site service disputes and analyzing client feedback for virtual assignments. The ideal candidate will ensure...
$30 - $37 per hour
...Job Title: Part Time Quality Assurance Specialist Job Description The Quality Assurance... ...Review manufacturing batch records and associated documentation to ensure accuracy, completeness... ...stakeholders. Contribute to document control activities to ensure that procedures,...Contract workTemporary workPart timeFlexible hours- ...Health and Safety requirements. II. Essential Functions: • Responsible... ...batch records, logbooks and other associated documents • Performs Quality verification of just-in-time labeling... ...in Quality programs, procedures and controls to ensure that products conform to established...Full timeContract workImmediate start
$85k - $105k
## Quality Associate, Batch Record Review and Product DispositionApplylocations: San Diegotime type: Full timeposted on: Posted 3 Days Agojob... ...Investigations, Product Complaints, Audit Responses, Change Controls, & Trainings) to ensure timely completion for the...Contract workTemporary workRemote workShift work- ...AI-Enabled Quality Systems | Biotech / GMP Environment Join a next-generation biotech organization redefining Quality Assurance through... ...What You’ll Do Own and maintain GMP / GxP SOPs, policies, and controlled documents across QA, QC, Manufacturing, and Clinical...
$33 - $35 per hour
...Assignment: 4-month contract Pay: $33–35/hr Schedule: Monday–Friday, 8:00 am – 5:30 pm About the Role Our client’s Quality Control team is seeking a Microbiology QC Analyst to support critical testing activities in a GMP environment. This role is ideal for...Contract workTemporary workMonday to Friday$25 - $31 per hour
...Job Title: Quality Assurance Specialist Salary Range: $25-31 Reports To: Quality Assurance Director Job Status: Exempt Non-Exempt Summary... ...improvement activities within the Centers for Disease Control, any State, and Federal requirements. The Quality Assurance Specialist...Remote workShift work$89.22k - $122.67k
...valuing your unique contributions. Responsibilities Providing Quality oversight of a US based site that manufactures and distributes... ...their personal information. To learn more, click here. Export Control: A successful candidate must be able to work with controlled technology...Temporary workLocal area$21.69 - $24.41 per hour
...from aseptic practices, personnel behaviors, or environmental controls that pose potential contamination risks. Capture detailed and objective... ...‑approved documentation tools or checklists. Collaborate with Quality Assurance, Operations, Microbiology, and Training to identify...Hourly payFull timeFlexible hours$60k - $85k
...Job Description Support Quality Assurance (QA) Batch Record Review, Product Disposition... ...appropriate QA updates. Maintain and update GMP controlled batch tracking tools, documentation... ...location is between $60,000-$85,000 for Associate level. The final wage offered to a...Contract work
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