CQV Engineers
Company: VTI Life Sciences
Location: Los Angeles
Posted on: February 16, 2026
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Job Description:
Job Description Job Description VTI Life Sciences (VTI) is
seeking forward-thinking and ambitious engineers looking to
accelerate their career 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 multiple CQV Engineers to
support our LA area client's project. We need 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
$40 - $60 PER HOUR AS A W2 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.
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Keywords: VTI Life Sciences, Covina , CQV Engineers, Engineering , Los Angeles, California
