Process Validation Engineer

Job Title : Process Validation Engineer

Lcation : CA United States

Experience : 5+ years

Contract : 12+ months

Job Overview :

We are seeking skilled professionals with expertise in CQV (Commissioning, Qualification, Validation), CSV (Computer Systems Validation), and Process Validation for contract opportunities in the pharmaceutical and medical device sectors. Opportunities are available for both early-career and experienced engineers.

Roles Available :

Junior to Senior Level Positions

Contract-based Opportunities

Pharma & Medical Device Industries

What We're Looking For :

CQV Engineers : Experience in commissioning, qualification, and validation of facilities, utilities, and equipment.

CSV Specialists : Expertise in validating computerized systems, ensuring compliance with FDA regulations, GxP, and 21 CFR Part 11.

Process Validation Engineers : Strong background in process development, risk analysis, and regulatory compliance within pharmaceutical or medical device manufacturing.

Key Requirements :

Solid experience in CQV, CSV, and / or Process Validation in pharmaceutical or medical device environments.

Strong knowledge of FDA regulations (e.g., 21 CFR Part 11, GxP) and industry standards.

Ability to collaborate with cross-functional teams and deliver projects on time.

For Senior Roles : Proven leadership experience in overseeing validation processes or leading validation teams.