fsttechnicalservices1mo ago
New
New
Validation Project Lead / Documentation Audit Lead
OtherProject Lead
0 views0 saves0 applied
Quick Summary
Overview
Validation Project Lead / Documentation Audit LeadMajor Pharmaceutical Facility Construction ProjectLocation: Durham,
Technical Tools
OtherProject Lead
Major 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
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.
Requirements
~1 min read- 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,
Location & Eligibility
Where is the job
Durham, United States
On-site at the office
Who can apply
US
Listing Details
- Posted
- July 30, 2026
- First seen
- September 25, 2026
- Last seen
- September 26, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 13%
- Scored at
- September 26, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
External application
Newsletter
Stay ahead of the market
Get the latest job openings, salary trends, and hiring insights delivered to your inbox every week.
A
B
C
D
No spam. Unsubscribe at any time.