VTI Life Sciences
Overview
CVQ Engineers
role at
VTI Life Sciences
– we are seeking forward-thinking and ambitious engineers to accelerate their career in the pharmaceutical, biotechnology and medical device industries. You will 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 and the candidate needs to reside locally to commute to the LA site
Responsibilities
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: equipment installation verification and confirmation that the equipment is installed in accordance with the manufacturer\'s specifications; document equipment installation and location
Operational Qualification: equipment functional verifications under operational conditions; conduct testing of equipment functionality and performance; document all test results and deviations
Performance Qualification: confirmation of the fractionation performance; validate the manufacturing process and critical process parameters; generate and review batch records and documentation
Process Validation: conduct process validation studies to ensure consistent product quality; perform risk assessments and implement process controls; develop and validate analytical methods for product testing
Cleaning Validation: validate cleaning procedures for the equipment to prevent cross-contamination; document cleaning validation protocols and results
Facility Qualification: conduct validation of critical facility systems
Compensation Hourly pay rate range for this role is
$40 - $60 per hour
as a W2
About VTI Life Sciences 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 competitive salary and benefits for our full-time/permanent employees.
www.validation.org
Seniority level
Entry level
Employment type
Full-time
Job function
Sales, General Business, and Education
Industries
Wireless Services, Telecommunications, and Communications Equipment Manufacturing
Referrals increase your chances of interviewing at VTI Life Sciences by 2x
Get notified about new Engineer jobs in
Los Angeles Metropolitan Area .
#J-18808-Ljbffr
role at
VTI Life Sciences
– we are seeking forward-thinking and ambitious engineers to accelerate their career in the pharmaceutical, biotechnology and medical device industries. You will 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 and the candidate needs to reside locally to commute to the LA site
Responsibilities
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: equipment installation verification and confirmation that the equipment is installed in accordance with the manufacturer\'s specifications; document equipment installation and location
Operational Qualification: equipment functional verifications under operational conditions; conduct testing of equipment functionality and performance; document all test results and deviations
Performance Qualification: confirmation of the fractionation performance; validate the manufacturing process and critical process parameters; generate and review batch records and documentation
Process Validation: conduct process validation studies to ensure consistent product quality; perform risk assessments and implement process controls; develop and validate analytical methods for product testing
Cleaning Validation: validate cleaning procedures for the equipment to prevent cross-contamination; document cleaning validation protocols and results
Facility Qualification: conduct validation of critical facility systems
Compensation Hourly pay rate range for this role is
$40 - $60 per hour
as a W2
About VTI Life Sciences 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 competitive salary and benefits for our full-time/permanent employees.
www.validation.org
Seniority level
Entry level
Employment type
Full-time
Job function
Sales, General Business, and Education
Industries
Wireless Services, Telecommunications, and Communications Equipment Manufacturing
Referrals increase your chances of interviewing at VTI Life Sciences by 2x
Get notified about new Engineer jobs in
Los Angeles Metropolitan Area .
#J-18808-Ljbffr