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Biotech Validation Jobs in California (NOW HIRING)

PSC Biotech

Validation Engineer I

San Francisco, CA · Remote

$20 - $23/hr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... This position will support system validation and product release processes, ensuring compliance ...

PSC Biotech

Validation QA Specialist

Pomona, CA · On-site

$110K - $120K/yr

At PSC Biotech ® , it's about more than just a job-it's about your career and your future. Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of ...

TekWissen LLC

QC Validation Specialist

Vacaville, CA · On-site

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: Validation Engineer II / QC Validation Specialist Location: Vacaville, CA, 95688 ...

Early-Stage biotech startup

Be Seen First

Research Scientist, Early-Stage Biotech Startup

San Diego, CA · On-site

$85K - $125K/yr

Research Scientist, Early-Stage Biotech Startup San Diego, CA 92128 | Full-Time or Part-Time | ... Biomarker discovery and validation * Uveal melanoma, retinoblastoma, DME, and AMD research

Kite Pharma

Sr Validation Engineer I

Oceanside, CA

Master's degree with 5+yearsof experience in validation in a biotech/pharma industry * Experience in GMP/cGMP-regulated environments * Extensive hands-on experience developing, executing, and ...

Cryoport

Validation Engineer

Irvine, CA · On-site

POSITION SUMMARY: The Validation Engineer - Consulting Services will support the Consulting ... ISO 21973 Biotechnology * General requirements for transportation of cells for therapeutic use ...

Cryoport

Validation Engineer

Irvine, CA

POSITION SUMMARY: The Validation Engineer - Consulting Services will support the Consulting ... ISO 21973 Biotechnology * General requirements for transportation of cells for therapeutic use ...

Cryoport, Inc.

Validation Engineer

Irvine, CA · On-site

POSITION SUMMARY: The Validation Engineer - Consulting Services will support the Consulting ... ISO 21973 Biotechnology * General requirements for transportation of cells for therapeutic use ...

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Infographic showing various Biotech Validation job openings in California as of August 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution.

CQV Validation Engineer, Biotech GMP Equipment - Remote (JP15497)

3 Key Consulting

Thousand Oaks, CA • Remote

$46 - $52/hr

Full-time

Re-posted 16 days ago

Job description

Job Title: CQV Validation Engineer, Biotech GMP Equipment – Remote (JP15497)
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: Engineering Systems
Duration: 12+ months with likely extensions and/or conversion to permanent
Posting Date: 06/16/2026
Pay Rate: $46 - $52/hour W2 with benefits
Notes: Fully Remote.
3 Key Consulting is hiring a C&Q Validation Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Primarily responsible for planning, coordinating, executing, and documenting periodic reviews of GMP equipment to ensure continued state of validation, compliance with regulatory requirements, and suitability for intended use.  The role partners with Engineering, Manufacturing, Quality Assurance, Validation, and Maintenance teams to assess equipment performance, maintenance history, calibration status, deviations, change controls, and overall lifecycle management.
Key skills and requirements:
• Demonstrable experience in a pharmaceutical, biotech, or life science organization in a C&Q/CQV/validation maintenance role.
• Knowledge of cGMP commissioning/qualification/validation practices.
• Familiarity with biotech/pharmaceutical manufacturing equipment.
• Familiarity with Kneat Gx Platform or other digital C&Q systems.
• Experience working with cross-functional stakeholders.
• Knowledge of quality assurance principles including deviations and change control systems.
• Effective communication skills, both verbal and written.
• Able to think analytically with the ability to resolve issues.
• Able to manage own time efficiently.
Position could be extended to up to 3 years
Why is the Position Open?
Planned Project.
Top Must Have Skills:
Experience in commissioning/qualification/validation, experience in a GMP environment, knowledge of biotech/pharmaceutical manufacturing equipment
Day to Day Responsibilities:
• Execute periodic reviews of GMP equipment according to approved procedures and schedules. Assess
 equipment records including work orders, deviations, and change control records.
• Evaluate equipment records to verify continued fitness for intended use.
• Generate and/or revise periodic review reports.
• Collaborate with Manufacturing, System Owners, Validation, and Quality teams as needed.
• Schedule and lead review meetings as needed to resolve issues.
• Ensure reviews are completed within established timelines and regulatory expectations.
• Maintain periodic review trackers and metrics.
• Identify opportunities to improve the equipment periodic review process.
• Other duties may be assigned to this role.
Basic Qualifications:
Master degree or Bachelor degree and 2 years of experience or Associate degree and 6 years of experience or high school diploma / GED and 8 years of experience
Employee Value Proposition:
Industry experience.
Red Flags:
Short tenures at previous jobs (<2 years)
No experience in commissioning/qualification/validation
Interview process:
1-2 Stages of interview | Video interview (Teams)
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.