Sr CQV and Packaging Engineer Thousand Oaks, CA

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/July2026
• Level of Experience: minimum 7years of CQV experience in the pharmaceutical/biotechnology industries
• Length of Project: Approximately 6months
• 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

• 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.

• Be an effective and independent seasoned leadcontributor that requires minimal to no supervision and delivers results.
• Bachelors 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 experiencein Packaging Validation including filling and capping process isolators drop test stress test andpackaging 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 Sciencesstrives 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.VTIoffers 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 organizationsVTIis 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.