🤖 15+ AI Agents working for you. Find jobs, score and update resumes, cover letter, interview questions, missing keywords, and lots more.
Cookies & analytics consent
We serve candidates globally, so we only activate Google Tag Manager and other analytics after you opt in. This keeps us aligned with GDPR/UK DPA, ePrivacy, LGPD, and similar rules. Essential features still run without analytics cookies.
Read how we use data in our Privacy Policy and Terms of Service.
🤖 15+ AI Agents working for you. Find jobs, score and update resumes, cover letter, interview questions, missing keywords, and lots more.
Jobs via Dice • Wilson, North Carolina, United States
Role & seniority: Lead Validation Engineer (senior/lead, 10+ years in validation; contract)
Stack/tools: Validation platforms (Kneat, GVault or equivalent); cGMP, FDA, EU regulatory frameworks; URS, DQ, IQ, OQ, PQ documentation
Lead planning, execution, and documentation of C&Q lifecycle for automation and process systems
Develop/implement validation strategies aligned with quality standards and regulatory requirements; mentor validation team
Coordinate cross-functional validation activities, review/approve protocols and reports, manage timelines and risk, support audits
Life sciences or engineering background; 10+ years in pharmaceutical/biotech validation
Proven leadership of C&Q projects and teams
Deep regulatory knowledge and validation best practices
Proficiency with Kneat, GVault, or equivalent; strong communication and stakeholder management
Experience with large-scale C&Q in regulated environments
PMP or equivalent project management certification
Prior lead experience on greenfield or brownfield validation projects
Location & work type: Wilson, NC; onsite, 5 days/week; contract-based engagement
Dice is the leading career destination for tech experts at every stage of their careers. Our client, Reveille Technologies, is seeking the following. Apply via Dice today!
Job Title: Lead Validation Engineer
Location: Wilson, NC (Onsite, 5 days a week)
Hiring Mode: Contract
Top 3 Must Have's: Life science Domain, Validation Skills, Delta V & MES Validation
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.
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.
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.
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.