Top 86 Quality control inspector Jobs in San Diego 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
QC Inspector III - 2nd Shift
5TH AXIS INC —San Diego, CA
- $32 - $37 an hour
- Background check
- 5 years
- Continuous improvement
Quick Apply
QC Inspector III - 1st Shift
5TH AXIS INC —San Diego, CA
- $32 - $37 an hour
- Background check
- 5 years
- Continuous improvement
Quick Apply
Metrology Technician
Fabric8Labs —San Diego, CA
- $25 - $30 an hour
- Weekends as needed
- Mid-level
- Analysis skills
- Travel
- Health insurance
- Dental insurance
Quick Apply
Quality Control Inspector Manufacturing (Not medical)
PlastiFab San Diego —Poway, CA
- $30 - $38 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Paid holidays
- Health insurance
Quick Apply
QA Associate I, Manufacturing
Catalent —San Diego, CA
- $60,000 - $70,000 a year
- Email
- Bachelor of Science
- High school diploma or GED
- Entry level
- Paid holidays
- Health insurance
Quality Control Inspector
IMIA, LLC —San Diego, CA
- $30 - $38 an hour
- Overtime
- Word processing
- Computer literacy
- Mid-level
- On-the-job training
Quality Inspector
Zenix Aerospace Inc —San Diego, CA
- $24.56 - $29.47 an hour
- Full-time
- Background check
- Microsoft Excel
- Computer literacy
- Tuition reimbursement
- 401(k) matching
Quality Technician
Fairbanks Morse Defense —National City, CA
- $30.22 - $36.03 an hour
- Weekends as needed
- Military
- English
- Mid-level
- Paid parental leave
- Paid holidays
Quality Inspector IV
BAE Systems Inc. —San Diego, CA
- $66,017 - $105,628 a year
- Full-time
- Construction site
- Computer literacy
- Mid-level
- Health savings account
- Paid holidays
5d
Quality Technician, Support ll, Evening Shift 2pm-10:30pm M-F
Zebra Technologies —San Diego, CA
- $25 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- Computer literacy
- Continuous improvement
- Paid time off
- Parental leave
4d
Quality Inspector -Union
BAE Systems Inc. —San Diego, CA
- Writing skills
- Mid-level
- High school diploma or GED
6d
Quality Control Inspector
Software Technology Inc —San Diego, CA
- Computer literacy
- High school diploma or GED
- Travel
Quick Apply
QA Associate III - Second Shift (2-10)
PCI Pharma Services —San Diego, CA
- $29.65 - $33.36 an hour
- Full-time
- ERP systems
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
Clinical - QA Associate, Clinical Studies
Medvacon Life Sciences, LLC —San Diego, CA
- $33 an hour
- 8 hour shift
- Mid-level
- Math
- Associate's degree
QC Inspector
Sherpa Clinical Packaging —San Diego, CA
- Entry level
QA Inspector
Software Technology Inc —San Diego, CA
- High school diploma or GED
- Travel
- Organizational skills
Quick Apply
Quality Specialist – Product Complaint Investigation and Analysis
Hologic —San Diego, CA
- $71,000 - $104,600 a year
- Inventory management
- Bachelor of Science
- Research
QC Technologist III
Werfen —San Diego, CA
- $34 - $39 an hour
- Online Application
- ERP systems
- Data analysis skills
- Maintenance
Quality Control Specialist I
ITT Inc. - English US —El Cajon, CA
- $20.77 - $30.77 an hour
- High school diploma or GED
- Communication skills
- Entry level
- Disability insurance
- 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

quality control inspector jobs in san diego ca

Quality Control Associate

QC Inspector III - 2nd Shift

QC Inspector III - 1st Shift

Metrology Technician

Quality Control Inspector Manufacturing (Not medical)

QA Associate I, Manufacturing

Quality Control Inspector

Quality Inspector

Quality Technician

Quality Inspector IV

Quality Technician, Support ll, Evening Shift 2pm-10:30pm M-F

Quality Inspector -Union

Quality Control Inspector

QA Associate III - Second Shift (2-10)

Clinical - QA Associate, Clinical Studies

QC Inspector

QA Inspector

Quality Specialist – Product Complaint Investigation and Analysis

QC Technologist III

Quality Control Specialist I

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