Top 5 Vti Instruments Jobs

Sr Lead CQV and CSV Engineer
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- Temporary
- 8 years
- Senior level
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- Full-time
- Computer literacy
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BAE Systems Inc. —Merrimack, NH
- $118,095 - $200,762 a year
- Full-time
- 5 years
- Mid-level
- Bachelor's degree
- Health savings account
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Product Line Manager
AMETEK, Inc. —Norwood, MA
- $125,000 - $140,000 a year
- 7 years
- Office
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Applications Engineer
AMETEK, Inc. —Norwood, MA
- $100,000 - $125,000 a year
- 5 years
- Mentoring
- US work authorization
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Sr Lead CQV and CSV Engineer

VTI Life Sciences
Thousand Oaks, CA

Quick Apply

Job Details

Temporary | Full-time

Qualifications

Quality control corrective actions
Data integrity assurance
GAMP
Laboratory equipment performance testing and validation
Pharmaceutical regulatory compliance
Preventive action implementation
Laboratory instrument validation
Production deviation management
Corrective and preventive actions (CAPA)
FDA 21 CFR Part 11
Manufacturing facility experience
Data integrity and documentation
Production validation processes
Quality risk management
Pharmaceutical company experience
Laboratory compliance
Leading team collaboration initiatives
Managing projects
Cross-functional team management
Pharmaceutical manufacturing facility experience

Full Job Description

Senior Validation Lead, CQV / CSV

We are seeking a Senior Validation Lead with strong experience supporting GMP qualification and validation programs across manufacturing equipment, facility utilities, QC laboratory systems, and computerized systems. This role should be capable of leading end-to-end validation lifecycle activities, authoring and reviewing validation deliverables, coordinating cross-functional teams, and ensuring compliance with FDA, cGMP, GAMP 5, 21 CFR Part 11, and data integrity expectations.

Key Responsibilities Lead commissioning, qualification, and validation activities for GMP manufacturing equipment, cleanrooms, utilities, and laboratory systems.
Develop, execute, and review validation lifecycle documentation, including Validation Plans, URS, Risk Assessments, Design Qualification, IQ/OQ/PQ protocols, traceability matrices, deviations, and final reports. Support Computer System Validation for laboratory and enterprise systems such as Empower, LIMS, ELN, Veeva Vault, TrackWise, Kneat, and related GxP platforms. Coordinate validation work with Engineering, QA, Manufacturing, Facilities, Automation, QC Laboratory, and Project Management teams.

Support FAT/SAT, calibration verification, qualification execution, discrepancy resolution, deviation investigation, CAPA, and change control. Apply risk-based validation practices aligned with ISPE, ASTM, GAMP 5, FDA 21 CFR Part 11, ALCOA+, and GMP requirements. Support qualification of equipment and systems such as freezers, isolators, biosafety cabinets, bioreactors, blenders, CIP/SIP skids, RO skids, HVAC, cold rooms, warehouse temperature mapping systems, chromatography systems, and QC laboratory instruments.

Required Experience 8+ years of validation experience in pharmaceutical, GMP manufacturing, or QC laboratory environments. Strong CQV background across equipment, utilities, facilities, laboratory instrumentation, and computerized systems. Hands-on experience with IQ, OQ, PQ, FAT, SAT, risk assessments, deviations, CAPA, and change control. Strong CSV experience with regulated laboratory and quality systems. Experience with 21 CFR Part 11, EU Annex 11, GAMP 5, data integrity, ALCOA+, cGMP, and GLP expectations. Ability to lead validation execution independently and manage multiple stakeholders. Preferred Systems / Tools Empower, LIMS, ELN, LabX, ChemStation, OMNIS Veeva Vault, TrackWise, Kneat MS Project or similar project tracking tools Ideal Candidate Profile The ideal replacement is not just a protocol executor. They should be a validation lead who can own documentation strategy, drive execution, resolve discrepancies, interface with QA and Engineering, and support both CQV and CSV workstreams in a regulated life sciences environment.
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Sr Lead CQV and CSV Engineer

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