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General Application - CQV, Staff Augmentation, and Regulatory Compliance - zD38lUWn3JTC-6411
General Application - CQV, Staff Augmentation, and Regulatory Compliance - zD38lUWn3JTC-6411-April 2024
Lenexa
Apr 2, 2026
About General Application - CQV, Staff Augmentation, and Regulatory Compliance - zD38lUWn3JTC-6411

  This job was posted by https://www.kansasworks.com : For moreinformation, please see: https://www.kansasworks.com/jobs/12813478CQV, On-Demand Staff Augmentation, and Regulatory Compliance

  (Pharmaceutical/Biotech)-Competitive Salary, Work/Life Balance!

  We offer Full and Part-Time W-2, 1099, and Agency Opportunities

  Previous Pharmaceutical/Biotech/Medical Device experience is mandatoryfor these roles.

  Are you looking to be a part of a close-knit work community? Do you haveexperience in the Life Science industry? Will you represent Compli, LLCas a CQV professional for our pharmaceutical manufacturing, biotech, andmedical device client projects? Do you enjoy traveling the country andmaking a difference? If so, this could be the right opportunity for you!

  The CQV Professionals will work closely with the client to provideinnovative solutions to our clients. We offer technical coaching in acollaborative environment that encourages employee growth anddevelopment. The ideal candidate will be a self-starter who takes pridein their work and actively pursues opportunities to learn and assistothers when needed.

  Hiring for these roles:

  Commissioning, Qualification & Validation (CQV)

  Experience in CQV with one or more of the following: facilities,utilities, equipment, computer-related systems, analytical instruments,analytic methods, cleaning validation, and process validation. We arelooking for the following:

  CQV Engineers/Specialists

  CQV Project Leads

  CQV Project Managers

  On-Demand Staff Augmentation

  Project Manager

  Senior Project Manager

  Systems Integration Consultant

  Regulatory Compliance

  Data Integrity Consultant

  Intern Opportunities

  Compli, LLC was founded in 2001 to provide commissioning,validation, and regulatory support services to the life sciencesindustry. We serve pharmaceutical companies across the U.S. Regardingregulations and compliance, it has never been more important tounderstand the documentation and quality assurance activities as theyrelate to vendors, engineering, construction, and contractors, which iswhy clients trust the Compli team.

  Perks of the Job:

  Competitive Pay commensurate with experienceWork / Life BalanceWorking with a small, close-knit team where you are valued as anindividualA learning environment and continuous advancement opportunitiesFeel overqualified? Feel underqualified? Apply anyway if this soundslike the fit you are looking for! We have flexibility in how we hire therole.

  To learn more and APPLY NOW: http://www.ucompli.com/careers

  Agencies, Compli welcomes your qualified candidates. Please [email protected] to establish a relationship with ourfirm.

  We are an equal opportunity employer M/F/D/V

  Job Keywords: Unites States, commission, qualification, validation,CQV, DQ, FATs, SATs, IQ, OQ, PQ, PVPs, URs, RTMs, CPPs, VPPs, ProjectValidation Plans, Lead qualification processes, Project Managers,Project Leads, Project Specialist, Project Engineers, ProjectProfessionals, Pharmaceutical, Life Science Industry, CQV, MMR,Pharmaceutical, Pharma, Biotech Industry, cGMP, Risk-based commission &qualification, Aseptic processing, Autoclaves, Lyos, Dry Heat Tunnel,HPLCs, FTIRs, GCs, UV Spectrophotometers, TOC Analyzers, Balances, dataintegrity, Part 11 compliance, HVAC systems, Facility roomqualification, utility validation, equipment validation, equipmentautomation, computer automation, cleaning validation, technical writing,SOPs

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