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Verista, Inc.

6490 - Senior C&Q Engineer / Senior Validation Engineer

Verista, Inc. · Devens, MA (Remote)

Posted 23 days ago

or apply directly on Verista, Inc.'s site. We never take the application ourselves.

Is this posting real?

This role has been open
23 days
Verista, Inc.'s roles stay open a median of 45 days
Reposted
No
Salary listed
No
0% of Verista, Inc.'s roles list one
Ghost-job risk at Verista, Inc.
high
21 stale, 0 reposted of 40 open
Hiring momentum
63 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-09-17

Measured from postings appearing on and disappearing from Verista, Inc.'s own greenhouse board since 2026-08-03. Full hiring picture for Verista, Inc..

About this role

The Senior Validation Engineer at Verista will lead and support Commissioning & Qualification (C&Q) activities for GMP facilities and systems throughout their project lifecycle. Responsibilities include developing and executing C&Q deliverables, coordinating execution activities, managing documentation, and ensuring compliance with GMP requirements. The role involves collaboration with various stakeholders and maintaining project trackers while supporting multiple concurrent C&Q projects.

Our read on this posting3.6out of 5
benefits
5/5
freshness
4/5
career value
4/5
role clarity
5/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Verista, Inc. as an employer.

What you need

  • Bachelor’s degree in Engineering, Life Sciences, or another industry-related technical discipline
  • 5+ years of experience in C&Q/CQV, commissioning, qualification, validation, engineering, or technical project execution within regulated pharmaceutical, biotech, or life sciences environments
  • Demonstrated hands-on experience with commissioning and qualification of GMP facilities, utilities, equipment, manufacturing systems, or laboratory systems
  • Strong working knowledge of C&Q methodologies and deliverables, including URS, DQ, FAT/SAT, commissioning, IQ/OQ/PQ, traceability, risk assessments, deviations, and qualification summary reports
  • Working knowledge of GMP, GEP, ASTM E2500, risk-based qualification, and Good Documentation Practices
  • Experience authoring, reviewing, and executing C&Q protocols, test scripts, commissioning documents, qualification reports, SOPs, work instructions, and other controlled documentation

Nice to have

  • Kneat Power User Level 1 (or higher) certification
  • Experience with HP ALM/Quality Center, Jira, or other project/test-management platforms
  • Experience with BMS, Documentum, Veeva Vault, or other electronic document management systems
  • Experience supporting large-scale pharmaceutical/biotech capital projects, facility expansions, equipment installations, or multi-site C&Q programs

What you get

  • High growth potential and fast-paced organization with a people-focused culture
  • 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
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance

Worth weighing

  • Remote role with limited travel to client sites
  • Salary range provided but dependent on various factors and subject to change
  • Role involves managing multiple concurrent projects which may be demanding

Summarised from Verista, Inc.'s posting. Read the full original.

Listed by Verista, Inc. on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

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