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Sr. CQV Engineer - Thousand Oaks, CA

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Inc. (Vti)
Full Time position
Listed on 2026-06-10
Job specializations:
  • Engineering
    Biomedical Engineer, Pharma Engineer, Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below

VTI Life Sciences (VTI) is seeking forward‑thinking and ambitious engineers to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to support teams of industry subject matter experts and consult with some of the largest companies in the Life Sciences industry.

We are looking for a Senior CQV Engineer to support a VTI client project in Thousand Oaks, CA. The ideal candidate has experience developing, executing, and reporting CQV protocols (IQ, OQ, PQ) for utility, HVAC, filling, and packaging systems.

HOURLY PAY RATE RANGE FOR THIS ROLE IS $90,000 - $120,000 ANNUALLY AS A W2

PROJECT OVERVIEW
  • Start:
    June/July 2026
  • Level of

    Experience:

    minimum 7+ years of CQV experience in the pharmaceutical/biotechnology industries
  • Length of Project:
    Approximately 12 months
  • 40 hours per week (Monday‑Friday)
  • This position is 100% onsite & the candidate needs to reside locally to commute to the Thousand Oaks client site
RESPONSIBILITIES
  • Develop and execute CQV protocols, reports, and risk assessments in accordance with client procedures and cGMP, FDA, EMA, and other regulatory guidelines.
  • Coordinate validation activities with Manufacturing and QA to ensure proper execution.
  • Investigate and support the resolution of protocol deviations and nonconformities.
  • Support change control activities related to system and equipment modifications.
  • Write and maintain SOPs related to system and equipment operation and maintenance.
  • Ensure documentation meets internal quality standards and audit readiness.
REQUIREMENTS
  • Bachelor’s degree or higher in Engineering, Chemistry, Pharmaceutical Sciences, or a related scientific field.
  • Minimum 7+ years of experience in the Biotechnology or Pharmaceutical industries.
  • Strong technical writing and protocol/report development skills.
  • Ability to interpret complex data and resolve validation issues.
  • Effective communication and cross‑functional collaboration skills.
  • Proficiency with validation lifecycle management systems and quality management systems (Track Wise, Kneat, Veeva, etc., a plus).

VTI Life Sciences strives to maintain and inspire professional excellence by providing Commissioning, Qualification, Quality Engineering, Automation, and Validation Services to the Pharmaceutical, Biotechnology, Biologics, and Medical Device industries. VTI offers professional development, training, competitive compensation, excellent benefits, a matching 401K, and a stimulating, collaborative work environment.

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