Sr CQV and Packaging Engineer - Thousand Oaks, CA VTI Life Sciences Thousand Oaks, CA Job Details Full-time 1 day ago Benefits 401(k) matching Qualifications Engineering stress testing Stress testing simulations Content creation for technical audiences Technical documentation Technical writing experience within manufacturing English Quality reports Production validation processes Pharmaceutical company experience Scientific protocols Packaging Data interpretation Cross-functional communication Pharmaceutical manufacturing facility experience Scientific reports Full Job Description VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences industry. We are looking for a Senior CQV Engineer to support a VTI client project in Thousand Oaks, CA. We need a Sr. CQV Engineer with experience developing, executing, and reporting CQV protocols (IQ, OQ, PQ) for utility, HVAC, filling, and packaging systems.

PROJECT OVERVIEW

Start:

June/July 2026

Level of Experience:

minimum 7+ years of CQV experience in the pharmaceutical/biotechnology industries

Length of Project:

Approximately 6 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 Be an effective and independent, seasoned lead contributor that requires minimal to no supervision and delivers results. 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 Minimum 3+ years of experience in Packaging Validation including filling and capping process, isolators, drop test, stress test and packaging systems. Strong technical writing and protocol/report development skills. Ability to interpret complex data and resolve validation issues. Effective english-native communication and cross-functional collaboration skills. Proficiency with validation lifecycle management systems and quality management systems (TrackWise, 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, plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in a work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm, and diligence. As one of the leading global Commissioning, Qualification, and Validation Services organizations, VTI is always looking for innovative, talented, and experienced validation professionals for our multinational and global offices. We offer some of the best salary and benefit packages in the industry for our full-time/permanent employees. www.validation.org HRUiLF3fm6