Top 2466 Documentation control 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
Quality Control Microbiology Associate
SMSbiotech, Inc —San Diego, CA
- $60,000 - $68,000 a year
- Full-time
- Driver's License
- Bachelor's degree
- Travel
- Mileage reimbursement
- Health insurance
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Lead Medical Radiation Physicist - Sharp James S. Brown-Outpatient Pavilion - Variable Shift - Full Time - Eligible for up to $20K in New Hire Incentives
SHARP HEALTHCARE —San Diego, CA
- 8 hour shift
- Outpatient experience
- Master's degree
- Doctor of Philosophy
- Referral program
6d
Inventory Control Manager
Saronic Technologies —San Diego, CA
- Full-time
- Office
- 8 years
- Senior level
- Paid parental leave
- Paid holidays
Quick Apply
Accounts Payable Specialist
Robert Half —San Diego, CA
- $30 - $35 an hour
- Contract
- Office
- US work authorization
- Organizational skills
- Disability insurance
- Dental insurance
Quick Apply
2d
Data Entry Specialist – Remote
True Legacy Homes —San Diego, CA
- $23.40 - $30.00 an hour
- Full-time
- Remote
- Google Workspace
- Administrative experience
- High school diploma or GED
- Dental insurance
- Paid time off
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15h
Help Desk Technical Support Specialist - East Coast Hours (5am to 2pm Pacific)
myCRE, Inc —San Diego, CA
- $50,000 - $70,000 a year
- Weekends as needed
- Remote
- Mid-level
- Windows
- High school diploma or GED
- Mileage reimbursement
- Health insurance
Quick Apply
Document Control Specialist II
Hill International, Inc —San Diego, CA
- $60,000 - $90,000 a year
- Hybrid work
- Writing skills
- Mid-level
- Microsoft Office
- Commuter assistance
- Health savings account
4d
Document Control Specialist
AMETEK, Inc. —San Diego, CA
- $55,000 - $70,000 a year
- Microsoft Excel
- Oracle
- Microsoft Outlook
- Health savings account
- Paid holidays
Technical Writer
Accenture Federal Services —San Diego, CA
- $91,300 - $109,100 a year
- Microsoft Word
- Mid-level
- Bachelor's degree
10d
Data Entry Operator
Orbis, Inc. —San Diego, CA
- $32,000 - $40,000 a month
- High school diploma or GED
- Entry level
- Under 1 year
Processor
NFM Lending —Encinitas, CA
- $24.04 - $31.25 an hour
- Overtime
- Remote
- Mid-level
- High school diploma or GED
- Continuous improvement
Document Control Clerk
Knowles —San Diego, CA
- $20 - $29 an hour
- Microsoft Excel
- Microsoft Outlook
- ERP systems
- Paid holidays
- Health insurance
Quick Apply
11d
Technical Documentation Coordinator
Rasirc —San Diego, CA
- $71,000 - $80,000 a year
- Full-time
- ERP systems
- Mid-level
- Organizational skills
- Health insurance
- Paid time off
Quick Apply
Assistant Program Coordinator — Enterprise Transformation
Solar Turbines —San Diego, CA
- $77,264 - $115,896 a year
- Full-time
- Pass drug screening
- Bachelor's degree
- Business
- Health savings account
- Paid holidays
3d
Data Center Technician
Introl —San Diego, CA
- $30 - $36 an hour
- Overtime
- Mid-level
- Ability to lift 50 pounds
- US work authorization
- Health insurance
- Dental insurance
Clinical Research Coordinator I
CAMRIS International, LLC —San Diego, CA
- $70,304 - $73,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Mid-level
- Health savings account
- AD&D insurance
Quality Control Analyst III
Oceaneering —San Diego, CA
- $41.88 - $62.84 an hour
- Full-time
- Microsoft Excel
- Mid-level
- High school diploma or GED
- Paid parental leave
- Health insurance
Specialist, Procurement
L3Harris Technologies —San Diego, CA
- $73,000 - $1,350,000 a year
- Microsoft Word
- Microsoft Outlook
- Mid-level
- Paid holidays
- Disability insurance
Medical Records Clerk
SAN DIEGO CENTER FOR CHILDREN —San Diego, CA
- $21 an hour
- Full-time
- Psychiatry
- Residential
- Administrative experience
- 403(b) matching
- Health insurance
Quick Apply

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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

documentation control jobs in san diego, ca

Quality Control Associate

Quality Control Microbiology Associate

Lead Medical Radiation Physicist - Sharp James S. Brown-Outpatient Pavilion - Variable Shift - Full Time - Eligible for up to $20K in New Hire Incentives

Inventory Control Manager

Accounts Payable Specialist

Data Entry Specialist – Remote

Help Desk Technical Support Specialist - East Coast Hours (5am to 2pm Pacific)

Document Control Specialist II

Document Control Specialist

Technical Writer

Data Entry Operator

Processor

Document Control Clerk

Technical Documentation Coordinator

Assistant Program Coordinator — Enterprise Transformation

Data Center Technician

Clinical Research Coordinator I

Quality Control Analyst III

Specialist, Procurement

Medical Records Clerk

I want to receive the latest job alert for documentation control in san diego, ca

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