Lead Validation Engineer

InterSources Logo
  • Production
  • FullTime
  • Applications have closed

Role: Lead Validation Engineer
Location: Wilson, NC (onsite)
Duration: Long Term ContractMust Have’s: Life science Domain, Validation Skills, Delta V & MES ValidationJob 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.

InterSources