Lead Validation Engineer

TechDigital

  • Wilson, NC
  • 27 days ago

    Highlights

    This leadership role is responsible for ensuring validation strategies align with regulatory expectations and project goals, while mentoring a team of validation professionals and coordinating with cross-functional stakeholders. Job Summary: The Lead Validation Engineer will oversee and drive commissioning and qualification (C&Q) activities for automation and process systems at a regulated manufacturing site.

    Numbers & Facts

    LocationWilson, NC
    IndustryOther/Not Classified
    Company Size100 to 499 employees

    Description

    Top 3 Must Have's: Life science Domain, Validation Skills, Delta V & MES Validation

    Job Summary:
    The Lead Validation Engineer will oversee and drive commissioning and qualification (C&Q) activities for automation and process systems at a regulated manufacturing site. This leadership role is responsible for ensuring validation strategies align with regulatory expectations and project goals, while mentoring a team of validation professionals and coordinating with cross-functional stakeholders.
    ________________________________________
    Key Responsibilities:
    • Lead the planning, execution, and documentation of C&Q lifecycle activities (URS, DQ, IQ, OQ, PQ) for automation and process systems.
    • Develop and implement validation strategies in alignment with quality standards and global regulatory requirements.
    • Serve as the primary point of contact for validation-related matters across engineering, QA, manufacturing, and automation teams.
    • Review and approve validation protocols, reports, and supporting documentation.
    • Manage validation timelines, resource allocation, and risk mitigation plans.
    • Provide technical leadership and mentorship to validation engineers and contractors.
    • Support audits and inspections by presenting validation documentation and processes.
    • Ensure compliance with cGMP, FDA, EU, and internal quality standards.
    ________________________________________
    Required Qualifications:
    • Bachelor's or Master's degree in Engineering, Life Sciences, or related field.
    • 10+ years of experience in validation within the pharmaceutical or biotech industry.
    • Demonstrated leadership in managing C&Q projects and teams.
    • Deep understanding of regulatory requirements and industry best practices.
    • Proficiency with validation tools such as Kneat, GVault, or equivalent.
    • Strong communication, organizational, and stakeholder management skills.
    ________________________________________
    Preferred Qualifications:
    • Experience with large-scale C&Q projects in regulated environments.
    • PMP or equivalent project management certification.
    • Prior experience leading validation efforts in greenfield or brownfield projects.

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