CQV Engineer

Stark Pharma Solutions Inc

  • Charlotte, NC
  • 6 days ago

    Highlights

    We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success. We are seeking a CQV Engineer with strong experience in pharmaceutical manufacturing and regulated environments to support commissioning, qualification, and validation activities for facilities, utilities, equipment, and systems.

    Numbers & Facts

    LocationCharlotte, NC

    Description

    About the Company

    Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

    Position: CQV Engineer

    Location: North Carolina

    Duration: Long Term

    Job Overview

    We are seeking a CQV Engineer with strong experience in pharmaceutical manufacturing and regulated environments to support commissioning, qualification, and validation activities for facilities, utilities, equipment, and systems.

    Key Responsibilities

    Develop, execute, and document commissioning and qualification protocols.
    Perform IQ, OQ, and PQ activities for equipment, utilities, and systems.
    Support commissioning and qualification of pharmaceutical manufacturing facilities and equipment.
    Prepare and maintain CQV protocols, reports, and validation documentation.
    Support FAT, SAT, commissioning, and qualification activities.
    Work with Engineering, Quality, Manufacturing, and Project teams to resolve CQV issues.
    Support deviations, investigations, change controls, and CAPA activities.
    Ensure CQV activities comply with GMP, FDA, and GxP requirements.
    Support continuous improvement and project execution activities.

    Required Qualifications

    Bachelor's degree in Engineering, Life Sciences, or a related technical field.
    3+ years of experience in CQV, Commissioning, Qualification, or Validation within the pharmaceutical or biotech industry.
    Hands-on experience with IQ/OQ/PQ activities.
    Experience with pharmaceutical facilities, utilities, equipment, or systems.
    Knowledge of GMP, FDA, GxP, and validation requirements.
    Experience preparing and executing CQV protocols and reports.
    Strong documentation, analytical, communication, and problem-solving skills.
    Ability to work effectively with cross-functional teams.

    How to Apply

    Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

    Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse
    backgrounds.

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