CQV Engineer: Validation & Compliance in Life Sciences

Verista, Inc.; Vista (CA); On-site; USD 74,000 - 118,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Matching

Paid Time Off

Tuition Reimbursement

Commuter Benefits

Life Insurance

Disability Insurance

PTO rollover

Job summary

Verista, Inc. is seeking a CQV Engineer with a strong background in validation within regulated pharmaceutical, biotechnology, or life sciences manufacturing. The role focuses on reviewing validation and qualification documentation to ensure accuracy, completeness, and regulatory compliance.

Ideal candidates have 3+ years of CQV experience and hands-on exposure to process equipment such as tanks and reactors. Join a team of 500 experts dedicated to solving healthcare challenges.

Qualifications

• 3+ years of validation/CQV experience in regulated manufacturing (pharma/biotech/medical device).
• Strong understanding of validation lifecycle: IQ/OQ/PQ/closeout.
• Experience reviewing validation docs, protocols, test scripts, deviations.

Responsibilities

• Review commissioning, qualification and validation documentation for accuracy and compliance.
• Verify that qualification activities meet procedures, specs, acceptance criteria and GMP requirements.
• Identify gaps and work with Engineering, Quality, Validation and Operations to resolve issues.
• Ensure GDP-compliant documentation and inspection readiness.
• Support validation activities as needed.

Skills

Validation expertise

GMP Knowledge

GDP Knowledge

Documentation review

Attention to detail

Cross-functional collaboration

Communication skills

Education

Bachelor’s degree in Engineering or Life Sciences

Job description

Verista, Inc. is seeking a CQV Engineer with a strong background in validation within regulated pharmaceutical, biotechnology, or life sciences manufacturing. The role focuses on reviewing validation and qualification documentation to ensure accuracy, completeness, and regulatory compliance.

Ideal candidates have 3+ years of CQV experience and hands-on exposure to process equipment such as tanks and reactors. Join a team of 500 experts dedicated to solving healthcare challenges.