CQV / CSV Engineer

Intellectt Inc; California (MO); Hybrid; USD 41,328 - 68,880; Part time

Job summary

A leading recruiting firm is on the lookout for a Sr. Pharma Recruiter to fill contract roles in CQV, CSV, and Process Validation in the pharmaceutical and medical device industries. Candidates will have a chance to work with cutting-edge technologies while ensuring regulatory compliance. The contract offers flexibility with both remote and on-site opportunities. Ideal candidates should hold a Master's degree in Biotechnology and possess relevant sector experience. Apply now to join this dynamic environment.

Qualifications

• Experience in CQV (Commissioning, Qualification, Validation), CSV (Computer Systems Validation) and Process Validation.
• Knowledge of FDA regulations (e.g., 21 CFR Part 11, GxP).
• Prior leadership experience is a plus for senior roles.

Responsibilities

• Ensure project deliverables are met through collaboration.
• Work with pioneering technologies in the pharma sector.

Skills

Experience in CQV, CSV, and Process Validation

Knowledge of FDA regulations

Collaboration with cross-functional teams

Education

Master Degree in Biotechnology

Job description

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

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!

Base pay range

$30.00/hr - $50.00/hr

• Experience in CQV, CSV, and/or Process Validation in the pharmaceutical or medical device sectors.
• Knowledge of FDA regulations (e.g., 21 CFR Part 11, GxP) and industry standards.
• Collaboration with cross-functional teams to ensure project deliverables are met.
• Senior roles: Prior leadership experience overseeing validation processes or leading validation teams.
• Contract type: Flexible contract roles across the US – remote and on-site opportunities.
• Special projects: Work with cutting‑edge technologies in pharma and medical device sectors; gain exposure to industry‑leading projects and enhance skillset.

Seniority level

• Associate

Employment type

• Contract

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.