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 Position Summary: ~ Work Schedule: Monday-Friday, core hours 8am-4:30pm ~100% on-site (San Diego... ...Updating documents related to Material Management Quality Control, Material Management Quality Assurance, Batch Records, Compliance...SuggestedContract workWork experience placementLocal areaWorldwideMonday to Friday$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$20.77 - $30.77 per hour
...various stages of the production process to ensure adherence to quality standards and specifications. You will identify defects,... ...of job safety analyses. This position requires visibility to controlled documents. Position Requirements Required: High school diploma...Hourly payTemporary workWork at office$49.84 per hour
...Quality Control Specialist (Contract)Pay Rate: Up to $49.84/hourDuration: Temporary Assignment — August 24, 2026 through December 18, 2026Hours: Full-TimeLocation: San Diego, CA (Onsite)SummaryWe are seeking a detail-oriented Quality Control Specialist to support quality...Contract workTemporary work$76.44k
...implement, and maintain the project-specific Quality Assurance Surveillance Plan (QASP) in... ...construction contractor’s Quality Control meetings (Preparatory, Initial, and Follow... ...not limited to, the role, function and associated responsibilities, relevant work experience...Contract workFor contractorsWork experience placementFor subcontractorH1bImmediate startFlexible hours- ...Quality Assurance Specialist Job Purpose The Quality Assurance Specialist is an experienced... ...works collaboratively with the QA Associate and Sr. Quality Systems Engineer. The QA... ...day-to-day administration for document control, training, and asset management, while...
$83.5k - $133.5k
...advance the release of effective, high-quality medicines, assure the safety of food and... ...to the continuous improvement of quality control processes and procedures. Adhere to all... ...BD, we reward, support and develop our associates through our comprehensive Total Rewards...Hourly payWorldwideShift work- ...REVA Medical, LLC. in San Diego, CA seeks a QA Associate to support the Quality Management System through document control, training administration, and asset maintenance. You will ensure record accuracy, track due dates, and escalate issues per procedures, collaborating...
- ...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...Contract workImmediate start
$35 - $50 per hour
...Quality Specialist II GROW WITH US AND STAY EXTRAORDINARY: Launch your career to new heights with Innoflight—one of San Diego's fastest-... ...and drive timely resolutions. WHAT YOU'LL NEED: ~ Associate's Degree or higher in Engineering, Electrical Engineering,...Hourly payWork at officeWork visaFlexible hours$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... ...team and ensure development of respective associates. $90,000 - $125,000 a year FLSA...Work at officeLocal area- ...Quality Assurance Associate Quality Assurance Associate – Document Control, Training, and Asset Management The Quality Assurance Associate supports the effective operation of the Quality Management System through accurate and timely administration of document control...
- ...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...
$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- ...Quality Assurance SpecialistPeregrine Team is hiring a Quality Assurance Specialist to support a growing biotech organization focused... ...ResponsibilitiesReview and approve batch records, deviations, and change controls in accordance with cGMP guidelinesSupport internal and external...
- ...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...
- ...Quality Assurance SpecialistThe quality assurance specialist assists in ensuring that medical devices meet established quality standards... ...activities, quality management systems, R&D and design control processes, validation processes, product releases, document control...
- ...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...
- ...CSD-JD-QA Associate – Clinical SuppliesThis is an on-site contract opportunity. Three months... ...and other associated documentsPerforms Quality verification of just-in-time labeling... ...SOPsParticipates in Quality programs, procedures and controls to ensure that products conform to...Contract workImmediate start
$85k - $105k
...Quality AssociateBe a part of a global team that is inspired to make a difference in the... ...rare patients.Position Summary:The Quality Associate supports Quality Operations through the... ...Complaints, Audit Responses, Change Controls, & Trainings) to ensure timely completion...Contract workTemporary workShift work$25 - $33.5 per hour
...more information, please go to , and follow us on X or LinkedIn . Reporting to the Quality Systems Specialist, the Quality Systems Associate will support document control, training, and quality systems activities, providing word processing, archival and electronic...Hourly payContract workTemporary workH1bWork at office- ...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...
- ...United StatesCompany: GrifolsPosted: 2026-08-17Grifols is seeking a Quality Assurance professional to ensure compliance with domestic and... ...teams to review documentation, approvals, and change controls, ensuring deadlines are met within budget.The role emphasizes development...
$108.03k - $140k
...countries and regions.Grifols Diagnostic Solutions is seeking a Senior Quality Assurance Specialist. The Sr Quality Assurance Specialist... ..., an equivalency could include 8 years of experience, an Associate’s degree with 6 years of experience, or a Master’s degree with...$85k - $93k
Position Summary The Quality Analyst is responsible for assisting in administration... ...Customer communication and leading the associated non-conformance investigations.... ...review, operational qualifications, document control, change control, risk management, etc)....Temporary workFor contractorsWork at officeLocal area$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
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