CQV Engineers
Listed on 2026-02-12
-
Engineering
Validation Engineer, Quality Engineering, Pharma Engineer, Process Engineer
We are looking for multiple CQV Engineers to support our LA area client's project. We are looking for CQV Engineers with CQV experience to provide execution support (IQ, OQ, PQ) for systems and equipment including process vessels, buffer vessels, filter presses, centrifuges, CIP skids, clean rooms, WFI, RO storage tank, cold and chilled alcohol loops, compressed air, nitrogen distribution, process transfer line and pool tank piping.
You must have experience in executing CQV protocols within pharmaceutical facilities and have written and executed protocols and protocol final reports.
PROJECT OVERVIEW
- Start:
August 2025 - Level of
Experience:
1 - 4 years - Length of
Contract:
Approximately 12 months - 40 hours per week (Monday-Friday)
- This position is 100% onsite & the candidate needs to reside locally to commute to the LA site
Responsibilities include but are not limited to the following:
Provide validation support (IQ, OQ, PQ) for process vessels, buffer vessels, filter presses, centrifuges, CIP skids, clean rooms, WFI, RO storage tank, cold and chilled alcohol loops, compressed air, nitrogen distribution, process transfer line and pool tank piping.
Installation Qualification
o Equipment installation verification and confirmation that the equipment is installed in accordance with the manufacturer's specifications
o Document equipment installation and location.
Operational Qualification
o Equipment functional verifications under operational conditions.
o Conduct testing of equipment functionality and performance.
o Documenting of all test results and deviations
Performance Qualification
o Confirmation of the fractionation performance
o Validate the manufacturing process and critical process parameters.
o Generate and review batch records and documentation.
Process Validation
o Conduct process validation studies to ensure consistent product quality.
o Perform risk assessments and implement process controls.
o Develop and validate analytical methods for product testing.
Cleaning Validation
o Validate the cleaning procedures for the equipment to prevent cross-contamination.
o Document cleaning validation protocols and results
Facility Qualification
o Conduct validation of critical facility systems
HOURLY PAY RATE RANGE FOR THIS ROLE IS $60 - $70 PER HOUR
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
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