Senior Lab CQV Engineer - Validate & Qualify Lab Systems

Verista, Inc.; Muskegon (MI); On-site; USD 69,000 - 95,000; Full time

Benefits offered by this job

Medical, Dental & Vision

401(k) Matching

Paid Time Off and Holidays

Tuition Reimbursement

Job summary

Verista is seeking a Senior Lab CQV / Senior Validation Engineer to qualify and validate laboratory instruments and systems in a regulated pharmaceutical or life sciences environment. You will execute IQ/OQ/PQ, draft validation documents, and collaborate with QA, lab personnel, and vendors to ensure compliant qualification.

This 100% on-site role in Muskegon, MI requires 4–6 years of CQV experience and strong knowledge of cGMP, 21 CFR Part 11, and risk-based validation.

Qualifications

• Bachelor’s degree in a relevant technical field and 4–6 years CQV experience.
• Hands-on qualification of laboratory instruments in a regulated cGMP environment.
• Knowledge of 21 CFR Part 11 and GxP compliance.

Responsibilities

• Execute IQ/OQ/PQ qualifications for lab instruments and systems.
• Interface with QA, vendors, and lab personnel to define scope and criteria.
• Draft validation plans, URS, risk assessments, and trace matrices.
• Maintain compliant qualification documentation per cGMP.
• Coordinate with cross-functional teams to meet schedules.
• Support data flow and system integrations in validated environments.

Skills

CQV experience

Technical writing

Communication

Problem solving

Independence

Education

Bachelor’s degree in engineering or life sciences

Tools

HPLC

GC

TOC analyzers

Spectrophotometers

Job description

Verista is seeking a Senior Lab CQV / Senior Validation Engineer to qualify and validate laboratory instruments and systems in a regulated pharmaceutical or life sciences environment. You will execute IQ/OQ/PQ, draft validation documents, and collaborate with QA, lab personnel, and vendors to ensure compliant qualification.

This 100% on-site role in Muskegon, MI requires 4–6 years of CQV experience and strong knowledge of cGMP, 21 CFR Part 11, and risk-based validation.