CQV / CSV/ Process Validation Engineer

Intellectt Inc

California (MO)

Hybrid

USD 41,328 - 61,992

Full time

14 days+

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Job summary

A leading recruitment firm is seeking a Sr. Pharma Recruiter for contract-based opportunities in validation roles within the pharmaceutical and medical device industries. The position requires expertise in CQV, CSV, and Process Validation, as well as a Master Degree in Biotechnology. Candidates will work on cutting-edge projects, with flexible remote and on-site options available.

Qualifications

Experience in CQV, CSV, or Process Validation in pharma or medical device sectors.
Strong knowledge of FDA regulations.
Prior leadership experience for senior roles.

Responsibilities

Coordinate and oversee validation processes.
Ensure compliance with industry standards.
Conduct risk analysis and process development.

Skills

CQV (Commissioning, Qualification, Validation)

CSV (Computer Systems Validation)

Process Validation

FDA regulations knowledge

Cross-functional collaboration

Education

Master Degree in Biotechnology

Job description

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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