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Quality Control Associate, I-II
San Diego, CA, US
Scientific
Bachelors Degree
Full Time, Temp to Hire
$26-40 per hour
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
San Diego, CA, US
$26-40 per hour
Experienced (Non-Manager)
Full Time, Temp to Hire
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Kelly® Science & Clinical is seeking a Quality Control Associate I-II for a direct hire opportunity with one of our clients, a biotechnology company in San Deigo, 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.
Workplace: Onsite in San Diego, CA
Pay:
- Quality Control Associate I: $26 – $32 per hour
- Quality Control Associate II: $30 – $40 per hour
Position title: Quality Control Associate, I-II
Position type: Contract-to-hire
Overview
Shape 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 opportunity for professional development and direct impact on transformative therapies.
Responsibilities
- Independently 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.
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Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.