A pharmaceutical client of ours is seeking an experienced Validation Specialist IV to support validation and qualification activities across the full validation lifecycle. This position plays a critical role in ensuring equipment, utilities, facilities, and cleaning/sterility systems meet GMP and regulatory requirements.

Key Responsibilities

• Define qualification and validation strategies for assigned projects.
• Coordinate and execute validation activities supporting facility operations.
• Perform Equipment/Utility/Facility Qualification, Cleaning Validation, and Steaming/Sterility Validation.
• Ensure all work aligns with regulatory expectations and site validation lifecycle standards.

Required Qualifications

• Minimum 7 years of validation experience (required).
• Strong, hands‑on background in equipment validation.
• Ability to work onsite 5 days per week in Vacaville, CA.
• No travel stipend or per‑diem is offered for this position.
  
  

Employment Details

• W2 candidates only (no C2C, no 1099).
• This is a full‑time onsite contract role.
• Local or self‑relocating candidates only, due to lack of travel/per‑diem support.
  
  

The expected compensation for this position is $75-$83 per hour (W2). Actual pay within this range will depend on experience, skills, and qualifications relevant to the role.