Pharma Validation Engineer — CQV & Protocols Lead

CAI; Sacramento (CA); On-site; USD 75,000 - 90,000; Full time

Benefits offered by this job

Comprehensive Health Insurance coverage

24 days of Paid Time Off

15% Company Contribution to 401K

Job summary

A professional services company is seeking a Validation Engineer to ensure successful completion of commissioning and qualification activities in regulated pharmaceutical settings. The role involves developing documentation, writing protocols, and collaborating across teams. Candidates should possess a Bachelor's degree in a science or engineering field and 2-4 years of related experience. This full-time position offers a salary range of $75,000 to $90,000 per year, with substantial benefits including health insurance and paid time off.

Qualifications

• 2–4 years’ experience in a regulated industry.
• Familiarity with ISPE Baseline Guide 5 is a plus.
• Experience in pharmaceutical manufacturing processes.

Responsibilities

• Develop documentation for CQV activities.
• Write and execute protocols for field verification.
• Plan and coordinate work within teams.

Skills

Commissioning and qualification

Documentation development

Technical communication

Problem-solving

Collaboration

Education

Bachelor’s degree in science or engineering

Job description

A professional services company is seeking a Validation Engineer to ensure successful completion of commissioning and qualification activities in regulated pharmaceutical settings. The role involves developing documentation, writing protocols, and collaborating across teams. Candidates should possess a Bachelor's degree in a science or engineering field and 2-4 years of related experience. This full-time position offers a salary range of $75,000 to $90,000 per year, with substantial benefits including health insurance and paid time off.