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CQV​/CSV​/Process Validation Engineer

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: Intellectt Inc
Full Time position
Listed on 2025-12-01
Job specializations:
  • Pharmaceutical
    Pharma Engineer, Validation Engineer, Quality Engineering
  • Engineering
    Pharma Engineer, Biomedical Engineer, Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 30 - 45 USD Hourly USD 30.00 45.00 HOUR
Job Description & How to Apply Below
Position: CQV / CSV/ Process Validation Engineer
Location: California

Get AI-powered advice on this job and more exclusive features.

Intellectt Inc provided pay range

This range is provided by Intellectt Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$30.00/hr - $45.00/hr

Direct message the job poster from Intellectt Inc

Sr. Pharma Recruiter | Master Degree in Biotechnology, Technical Recruiting, Biology subject expert

We are actively seeking talented professionals with experience in CQV (Commissioning, Qualification, Validation),
CSV (Computer Systems Validation), and Process Validation for exciting contract roles in the pharmaceutical and medical device industries. Whether you are just starting out or are a seasoned expert, we want to hear from you!

📝 Roles Available:

  • Junior to Senior Level Positions
  • Contract-based Opportunities
  • Pharma & Medical Device Industries
  • CQV Experts – Experience in commissioning, qualification, and validation of facilities, utilities, and equipment.
  • CSV Specialists – Expertise in validating computerized systems, ensuring compliance with FDA, GxP, and 21 CFR Part 11.
  • Process Validation Engineers – Strong background in process development, risk analysis, and regulatory compliance in pharma or medical device manufacturing.
  • Solid experience in CQV, CSV, and/or Process Validation in the pharmaceutical or medical device sectors.
  • Strong knowledge of FDA regulations (e.g., 21 CFR Part 11, GxP) and industry standards.
  • Ability to collaborate with cross-functional teams and ensure project deliverables are met.
  • For Senior Roles:
    Prior leadership experience in overseeing validation processes or leading validation teams.
  • Flexible contract roles across the US –
    remote and on-site opportunities.
  • Work with cutting-edge technologies in the pharma and medical device sectors.
  • Gain exposure to industry-leading projects and enhance your skillset.

If you have experience in CQV
, CSV
, or Process Validation
, and you’re looking for a dynamic, contract-based role, we want to hear from you!

👉
Apply Now! Share your resume and we’ll connect to discuss the right opportunity for you.

Seniority level
  • Associate
Employment type
  • Contract
Job function
  • Quality Assurance
Industries
  • Biotechnology Research
  • Pharmaceutical Manufacturing
  • Medical Equipment Manufacturing

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