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Lead CQV Engineer​/Lead Validation Engineer

Job in Harvard, Worcester County, Massachusetts, 01451, USA
Listing for: Verista, Inc.
Full Time position
Listed on 2026-05-20
Job specializations:
  • Engineering
    Validation Engineer, Pharma Engineer
Salary/Wage Range or Industry Benchmark: 87780 - 140000 USD Yearly USD 87780.00 140000.00 YEAR
Job Description & How to Apply Below
Position: 6333 - Lead CQV Engineer / Lead Validation Engineer
Location: Harvard

Description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision‑making and are the result of our significant investment in our people and our capabilities.

Company

Culture Guidelines & Values
  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise
Responsibilities
  • Lead second shift CQV execution activities across multiple systems and work streams
  • Coordinate daily execution priorities to recover schedule slippage and maintain timelines
  • Interface with QA, Engineering, and Operations to resolve issues in real time
  • Oversee execution of IQ/OQ protocols and operational verification activities
  • Support and review:
    • Drawing walkdowns
    • Equipment and component verification
    • Materials of Construction (MOC) and weld verification
  • Provide oversight for temperature mapping and validation activities
  • Support SIP/CIP and related cycle development activities as needed
  • Ensure all documentation meets GMP/GDP and audit‑ready standards
  • Drive deviation identification, escalation, and resolution
Job Requirements
  • Bachelor’s Degree or equivalent required (STEM degree, Biomedical Engineering, Chemical Engineering preferred)
  • 8+ years of CQV/validation experience in pharma or biotech
  • Strong hands‑on execution background with process equipment (bioreactors, filtration, chromatography, UF)
  • Proven experience leading validation teams or shift‑based execution efforts
  • Strong GMP/GDP knowledge
  • Experience with eVal (required), Val Genesis a plus
  • Experience with temperature mapping (Ellab a plus)
  • Must be able to work second shift (2‑10 PM EST) and weekends

This role requires the ability to be on‑site, full‑time in Devens, MA.

Salary Range: $87,780 - $140,000 USD

* Verista is an equal opportunity employer.

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