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. www.validation.org [http://www.validation.org]
