Validation Project Lead / Documentation Audit Lead
•Today
| Estimated Pay info | Based on similar jobs in your market$53 per hour |
|---|---|
| Hours | Full-time |
| Location | Durham, North Carolina |
About this job
Job Description
Job Description
Validation Project Lead / Documentation Audit LeadMajor Pharmaceutical Facility Construction Project
Location: Durham, NC - FST Life Science office
FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a large pharmaceutical manufacturing facility construction project.
This role is responsible for establishing a standardized process for the validation of hygienic welding documentation (Isometrics) to ensure compliance with project specifications, applicable codes (e.g., ASME BPE), and industry best practices to support full traceability for hygienic systems..
Responsibilities
Validation Project Lead / Documentation Audit LeadMajor Pharmaceutical Facility Construction Project
Location: Durham, NC - FST Life Science office
FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a large pharmaceutical manufacturing facility construction project.
This role is responsible for establishing a standardized process for the validation of hygienic welding documentation (Isometrics) to ensure compliance with project specifications, applicable codes (e.g., ASME BPE), and industry best practices to support full traceability for hygienic systems..
Responsibilities
- Lead documentation audit activities to ensure full traceability of hygienic piping systems.
- Manage schedule, priorities, milestones, and deliverables.
- Audit weld documentation packages for GMP and Good Documentation Practices (GDP) compliance.
- Ensure document traceability.
- Coordinate resolution of documentation deficiencies and quality observations.
- Partner with Construction Management, Fabricators and Client representatives.
- Maintain validation metrics and documentation status reports.
- Mentor junior validation specialists and documentation specialists.
- Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related technical discipline (or equivalent experience).
- 8+ years of pharmaceutical validation, CQV, QA, or GMP documentation experience.
- 3+ years leading validation documentation or CQV teams on large pharmaceutical capital projects.
- Strong knowledge of FDA cGMP regulations (21 CFR Parts 210 & 211).
- Thorough understanding of Good Documentation Practices (GDP).
- Experience supporting Commissioning, Qualification & Validation activities.
- Experience preparing projects for client and regulatory audits.
- Excellent project management, organization, and communication skills.
- Experience with Traceability Matrices, ALCOA+, Equipment & Utilities Installation Qualification,
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Full-time Jobs Part-time Jobs Gig Jobs Posting ID: 1288512190 Posted: 2026-09-22 Job Title: Validation Project Lead Documentation