Top 83 Qa qc Jobs in Oceanside, Ca

Quality Control Associate
SMSbiotech, Inc —San Diego, CA
- $60,000 - $68,000 a year
- Full-time
- Data analysis skills
- Mid-level
- Driver's License
- Mileage reimbursement
- Health insurance
Quick Apply
Head of Quality
Gallant —San Diego, CA
- From $175,000 a year
- Weekends as needed
- Background check
- Master's degree
- 8 years
- Health insurance
- Dental insurance
Quick Apply
Softgel Manufacturing Supervisor
Nordic Naturals —Vista, CA
- $70,000 - $80,000 a year
- English
- Mid-level
- 3 years
Quality Assurance Manager
North South Consulting Group —Camp Pendleton, CA
- Full-time
- HIPAA
- Mid-level
- 3 years
Quick Apply
Quality Control Associate, Raw Material
Argonaut Manufacturing Services —Carlsbad, CA
- $33 - $45 an hour
- 8 hour shift
- 5 years
- Bachelor of Science
- Mid-level
- Health savings account
- Paid holidays
Quick Apply
QC Technologist III
Werfen —San Diego, CA
- $34 - $39 an hour
- Online Application
- ERP systems
- Data analysis skills
- Maintenance
9d
Chemist
Bachem Holding AG —Vista, CA
- $31.07 - $45.77 an hour
- Full-time
- Microsoft Excel
- Computer literacy
- Bachelor's degree
- Health insurance
- Dental insurance
Quality Control Associate, Raw Materials
Capricor Therapeutics —San Diego, CA
- $70,000 - $87,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
- Paid parental leave
- AD&D insurance
Quick Apply
Quality Control Inspector III
Abbott Laboratories —Temecula, CA
- $17.85 - $35.75 an hour
- Full-time
- High school diploma or GED
- Warehouse
- In-person
- Health insurance
- Tuition reimbursement
Design Quality Engineer
Enovis —Carlsbad, CA
- Full-time
- Hybrid work
- Microsoft Word
- Engineering
- 3 years
- Health insurance
- Dental insurance
Commercial Manufacturing Team Member
Bachem Holding AG —Vista, CA
- $70,658 - $97,155 a year
- Full-time
- Mid-level
- Analysis skills
- Bachelor's degree
- Health insurance
- Dental insurance
Quality Control Specialist, Analytical
Capricor Therapeutics —San Diego, CA
- $100,000 - $120,000 a year
- Full-time
- 5 years
- Mid-level
- Bachelor's degree
- Paid parental leave
- AD&D insurance
Quick Apply
Direct Materials Regulatory Filings Principal Expert
Genentech —Oceanside, CA
- $114,700 - $212,900 a year
- Online Application
- Bachelor of Science
- Office
- 8 years
9d
Principal Scientist
Merck KGaA —Carlsbad, CA
- $113,000 - $169,600 a year
- Bachelor of Science
- 11+ years
- Analysis skills
- Health insurance
- Paid time off
Survey Technician
NV5 —San Marcos, CA
- $25 an hour
- Extended hours
- Heavy lifting
- Mid-level
- Ability to lift 50 pounds
- Health insurance
- Dental insurance
2d
Quality Control Manager (QCM), Federal Construction
Elite Recruiting & Consulting Services —Temecula, CA
- Full-time
- Construction site
- 5 years
- Driver's License
- Health insurance
- Paid time off
Quick Apply
Director - UG Transmission Engineering
NV5 —San Diego, CA
- $180,000 - $250,000 a year
- Full-time
- Bachelor of Science
- 8 years
- Quality control
- Health insurance
- Dental insurance
9d
Senior Project Manager
PowerFlex —San Diego, CA
- $128,610 - $157,190 a year
- Full-time
- Hybrid work
- Clean driving record
- Microsoft Excel
- Construction site
- Health insurance
- Dental insurance
2d
Manager, Materials Management Buyer/Planner
Artiva Biotherapeutics —San Diego, CA
- $130,000 - $145,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Contracts
- Paid holidays
- Disability insurance
Quick Apply
4d
Scientist 3, Analytical Development
Catalent —San Diego, CA
- $115,000 - $125,000 a year
- Email
- Bachelor of Science
- Bachelor's degree
- Doctor of Philosophy
- Paid holidays
- Health insurance

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Quality Control Associate

SMSbiotech, Inc
San Diego, CA

Quick Apply

Job Details

Full-time
$60,000 - $68,000 a year

Benefits

Mileage reimbursement
Health insurance
Dental insurance
401(k)
Vision insurance

Qualifications

Data integrity assurance
Biology
Cell line culture
Teamwork
Data analysis skills
Good documentation practices (GDP)
Flow cytometers
Bachelor's degree
Attention to detail
Sterile laboratory techniques
Cytometry
FDA regulations

Full Job Description

Position Summary

SMS Biotech is a cell therapy company advancing an allogeneic stem-cell program for COPD, manufactured under cGMP at our Sorrento Valley biomanufacturing facility. We are seeking a hands-on Quality Control (QC) Associate to perform release and characterization testing of our cell therapy product, with a primary focus on potency assays and flow cytometry, and to perform final product vial inspection prior to shipment.

The QC Associate is primarily responsible for executing potency assay testing and flow cytometry-based analysis, and for performing pre-shipment vial checks to confirm that finished product meets specification before release for distribution. The Associate will also support general laboratory associate duties (e.g., tissue culture, media and reagent preparation, sample management) as needed, but the core focus of the role is QC testing and final vial verification before shipping. We are looking for a detail-oriented, self-directed learner who thrives in a fast-paced, growing GMP environment.

Key Responsibilities

Potency & QC Analytical Testing

· Perform potency assay testing of cell therapy product to support lot release and stability, following approved SOPs and compendial/validated methods.

· Execute cell-based and analytical assays accurately and contemporaneously, recording all data per Good Documentation Practices (GDP).

· Prepare samples, standards, controls, reagents, and media required for potency and release testing; manage reference standards and controlled stocks.

· Review assay results against acceptance criteria; flag out-of-specification (OOS) or atypical results and support investigations, deviations, and CAPA as needed.

· Support method qualification, validation, and transfer for new or improved QC assays.

Flow Cytometry

· Perform flow cytometry-based identity, viability, purity, and characterization testing of cell therapy product and in-process samples.

· Perform routine instrument startup, quality/calibration checks, and basic troubleshooting; escalate instrument issues and maintain instrument logs.

Vial Inspection & Release for Shipment

· Perform final visual inspection and vial checks of finished product (e.g., fill, cap/crimp integrity, labeling, appearance, and absence of defects) prior to release for shipment.

· Verify that vials and associated documentation are complete, accurate, and meet specifications before product is released for distribution.

· Support cold-chain and Good Distribution Practice (GDP) requirements — confirm storage and shipping conditions (e.g., LN2/cryogenic or cold-chain), monitor temperature excursions, and ensure proper handling of cryopreserved product.

· Document release-for-shipment activities and partner with QA to ensure product is shipped only after all QC checks are satisfied.

General Laboratory Support (as needed)

· Perform tissue culture/cell culture work in support of potency assays and routine QC operations, maintaining aseptic technique and cell-line health.

· Support media and reagent preparation, labeling, inventory, sample receipt and logging, and routine equipment maintenance and calibration.

· Assist manufacturing and laboratory associates with general lab tasks during peak workloads, while keeping QC testing and vial checks as the priority.

Quality, Documentation & Data Integrity

· Execute all work in compliance with cGMP, applicable SOPs, and data integrity (ALCOA+) requirements.

· Maintain right-first-time, contemporaneous documentation in test records, logbooks, and electronic systems per GDP and Good Distribution Practice.

· Author and revise SOPs, forms, and test records; maintain equipment logs and calibration records.

· Support internal and regulatory (FDA) audit and inspection readiness for the QC function.

Qualifications – Required

· Bachelor's degree in Biology, Biochemistry, Immunology, Microbiology, or a related life science.

· 1–3 years of hands-on laboratory experience, preferably in a GMP, pharmaceutical, biotech, or cell-therapy environment (relevant internship or co-op experience considered).

· Hands-on mammalian tissue culture/cell culture experience with strong aseptic technique.

· Experience with, or strong working knowledge of, flow cytometry (sample preparation, acquisition, and data analysis).

· Familiarity with cGMP documentation practices and data integrity (ALCOA+) principles.

· Strong attention to detail and the ability to perform precise, repeatable work and accurate, contemporaneous documentation.

· Ability to lift up to ~25 lbs, stand for extended periods, and perform detailed work requiring manual dexterity and color discrimination.

Qualifications – Preferred

· Hands-on experience performing potency or other cell-based release assays in a regulated (GMP) setting.

· Experience with cryopreservation, LN2/cold-chain handling, and final product visual inspection or release activities.

· Working knowledge of 21 CFR Parts 210/211 and 1271, USP compendial methods, and ICH quality guidelines.

· Experience supporting method qualification/validation, technology transfer, or new-assay build-out.

· Valid driver's license and willingness to travel occasionally between the Sorrento Valley and San Marcos sites (mileage/travel reimbursement provided).

What We're Looking For

· A self-starter and quick, independent learner who can pick up new assays and procedures with limited supervision.

· Comfortable working in a fast-paced, evolving environment and adapting to shifting priorities.

· Strong attention to detail, organization, and right-first-time documentation discipline.

· Reliable, accountable, and a collaborative team player who communicates clearly across functions.

· Flexibility to occasionally adjust hours to support manufacturing, testing, and shipping schedules.

What We Offer

· Hands-on experience in a cGMP cell-therapy program with a clear path for skill and career growth.

· The opportunity to grow your scope across potency, flow cytometry, and final product release testing.

· Travel and mileage reimbursement for any cross-site travel between Sorrento Valley and San Marcos.

SMS Biotech is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any legally protected status. This job description is intended to convey information essential to understanding the scope of the position and is not an exhaustive list of duties; responsibilities may evolve as the QC function grows.

Pay: $60,000.00 - $68,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Vision insurance

Education:

Bachelor's (Required)

Ability to Commute:

San Diego, CA 92121 (Required)

Work Location: In person

Quick Apply

Refine Your Search

qa qc jobs in oceanside, ca

Quality Control Associate

Head of Quality

Softgel Manufacturing Supervisor

Quality Assurance Manager

Quality Control Associate, Raw Material

QC Technologist III

Chemist

Quality Control Associate, Raw Materials

Quality Control Inspector III

Design Quality Engineer

Commercial Manufacturing Team Member

Quality Control Specialist, Analytical

Direct Materials Regulatory Filings Principal Expert

Principal Scientist

Survey Technician

Quality Control Manager (QCM), Federal Construction

Director - UG Transmission Engineering

Senior Project Manager

Manager, Materials Management Buyer/Planner

Scientist 3, Analytical Development

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