Quality Control Associate, I-II

Get AI-powered advice on this job and more exclusive features.This range is provided by Kelly. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.Base pay range$26.00/hr - $40.00/hrDirect message the job poster from KellySenior Recruiter | Biotech Enthusiast and Talent Partner | PhD-level Scientist | Working Parent | Immigrant | Helping scientists answer the…Kelly® Science & Clinical is seeking a Quality Control Associate I-II for a contract-to-hire opportunity with one of our clients, a biotechnology company in San Diego, CA, focused on neurological disorders. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.Pay rate:Quality Control Associate I: $26 – $32 per hourQuality Control Associate II: $30 – $40 per hourPosition title: Quality Control Associate, I-IIPosition type: Contract-to-hireOverviewShape the future of cell therapy in neurology as a Quality Control Associate II with one of San Diego’s dynamic and innovative biotechnology teams. You’ll play a vital role in supporting clinical-stage therapies powered by cutting‑edge science using induced pluripotent stem cells (iPSC), advancing treatments for neurological conditions.As a QC Associate II, you will execute essential quality control operations and testing to uphold cGMP standards in a collaborative, growth‑oriented environment. Your expertise will be instrumental in environmental monitoring, sample retention, and QA‑driven testing—directly supporting groundbreaking clinical trials. This position provides an opportunity for professional development and direct impact on transformative therapies.ResponsibilitiesIndependently perform QC testing of raw materials, intermediates, drug products, and stability samples according to validated protocols and procedures.Generate and deliver reliable cGMP‑compliant data, reports, and documentation.Actively contribute to assay development, qualification, optimization, and troubleshooting projects.Author, revise, and enhance SOPs, technical reports, and protocols—supporting program stability and regulatory compliance.Lead and support investigations into laboratory deviations and out‑of‑specification results, driving resolution and continuous improvement.Organize, maintain, and support clinical and raw material sample retention programs to ensure efficient lab operations.Own the raw materials inspection program—identifying and implementing workflow efficiencies.Support onboarding of new raw materials, guaranteeing strict compliance with SOPs and cGMP requirements.Perform laboratory maintenance: equipment, inventory, and general upkeep to exceed industry standards.Drive innovation by identifying opportunities for process improvements within the QC laboratory.Collaborate across functions and teams to meet dynamic timelines.Participate in other projects as needed, fostering your own development and the success of high‑priority initiatives.Qualifications & Experience:B.S. or M.S. in Biology, Cell Biology, Microbiology, Molecular Biology, Biochemistry, or a related scientific discipline.Minimum 2 years of laboratory experience in academic, clinical, or industrial settings.Prior experience in QC laboratories within cGMP‑regulated environments strongly preferred.Technical expertise with flow cytometry, real‑time PCR, cell culture, and molecular biology techniques.Exceptional attention to detail and organization, particularly in documentation and reporting.Initiative and adaptability in a fast‑paced, high‑impact setting.Team‑focused mindset with proven effectiveness working independently.Strong verbal and written communication skills—supporting effective cross‑functional collaboration.Comfortable with Microsoft Office Suite, especially Word, Excel, and PowerPoint.Flexibility to work occasional weekends and adapt hours as needed.Why Join Us?Contribute to therapies at the forefront of regenerative medicine and cellular neuroscience.Collaborate with leaders and experts in the biotech industry.Grow your career in a vibrant biotech ecosystem, surrounded by talented professionals.Ready to advance your impact in San Diego’s biotech sector? Apply today and help shape the future of medicine.What happens next?Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.Seniority levelAssociateEmployment typeContractJob functionQuality Assurance, Analyst, and ScienceBiotechnology Research and Pharmaceutical ManufacturingReferrals increase your chances of interviewing at Kelly by 2xGet notified about new Quality Control Associate jobs in San Diego, CA.Quality Control Associate I, Flow Cytometry (PM Shift)Research Associate – iPSC Culture (Contract)San Diego Metropolitan Area $63,000.00-$85,000.00 5 days agoQuality Control I/Lab (Required Flow Cytometry Exp) Entry Level - Urgent NeedQuality Control Associate - (Need Flow Cytometry, Tissue Culture, Lab Exp)San Diego Metropolitan Area $28.00-$32.00 4 days agoResearch Associate/Associate Scientist, Discovery Biology (Contract Position)We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr