Lead CQV Engineer/Analyst

7 days ago


New Brunswick, New Jersey, United States Verista Full time
Job Overview

Verista is seeking a highly skilled Lead CQV Engineer/Analyst to join our team. As a key member of our organization, you will be responsible for ensuring the quality and compliance of our products and processes.

Key Responsibilities
  • Develop and execute commissioning, qualification, and validation protocols for production equipment.
  • Lead risk assessments to identify and mitigate potential equipment compliance risks.
  • Collaborate with engineering and project teams to align validation activities with construction schedules.
  • Ensure all validation documentation complies with regulatory standards (FDA, cGMP).
  • Develop and execute IQ/OQ/PQ protocols for clean utilities and facility systems.
Requirements
  • Bachelor's degree in Engineering, Life Sciences, or related field.
  • 10+ years of experience in validating production equipment in pharmaceutical environments.
  • Expertise in isolators, bioreactors, fume hoods, and other lab equipment.
  • Strong knowledge of regulatory requirements and risk-based validation approaches.
  • Excellent project management and problem-solving skills.
What We Offer
  • Competitive pay plus performance-based incentive programs.
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances.
  • FSA, DCARE, Commuter Benefits.

Verista is an equal opportunity employer. We are committed to creating a diverse and inclusive work environment. If you are a motivated and detail-oriented individual who is passionate about quality and compliance, we encourage you to apply for this exciting opportunity.



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