6500 - Lead CQV Engineer / Lead Validation Engineer
Verista, Inc. · Wichita, KS (Hybrid)
Posted 16 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
- 16 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 Lead CQV Engineer will lead and execute validation and qualification activities in GxP-regulated environments, focusing on facilities, utilities, and laboratory systems. Responsibilities include authoring and reviewing validation documents, coordinating with various stakeholders, and ensuring compliance with regulatory requirements. The role also involves mentoring junior engineers and improving validation processes.
- 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 a related technical discipline
- 7+ years of validation/CQV experience within the pharmaceutical, biotechnology, medical device, or other regulated life sciences industries
- Demonstrated hands-on experience with both authoring and execution of validation and qualification deliverables
- Strong experience developing and executing IQ/OQ/PQ protocols, validation test scripts, commissioning documentation, and validation/qualification reports
- Experience leading validation activities across manufacturing equipment, process equipment, facilities, utilities, laboratory systems, automation, or computerized systems
- Strong understanding of cGMP requirements, validation lifecycle principles, and risk-based validation approaches
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
- Hybrid role requiring on-site presence between Wichita, KS and Boston, MA may be required
- Salary range provided is broad and dependent on various factors, with no specific figure guaranteed
- The role involves significant responsibility and project management, which may be challenging for less experienced candidates
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.
More roles at Verista, Inc.
- 6481 - Sr. Engineering Project Manager / Senior Project ManagerColumbus, OH
- 6485 - Project Engineer / Project Engineer 2Indianapolis, IN
- 6487 - Veeva LIMS SME Consultant / Lead Information Systems EngineerIndianapolis, IN
- 6486 - Project Controls Administrator / Project CoordinatorColumbus, OH
- 6490 - Senior C&Q Engineer / Senior Validation EngineerDevens, MA (Remote)
- 6497 - Business Analyst, Veeva Migration / Business AnalystRemote
- 6502- Automation Engineer / Automation EngineerIndianapolis, IN
- 6495 - Senior CQV Engineer / Senior Validation EngineerMount Vernon, IN