Validation Project Lead / Documentation Audit Lead
Durham, NCJobSeen 2mo agoSeen in employer's feed 4 days ago
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Job overview
FST Technical Services is hiring a Validation Project Lead / Documentation Audit Lead. FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a large pharmaceutical manufacturing facility construction project, establishing a standardized process for validation of hygienic welding documentation to ensure compliance with specifications, codes and best practices.
Key focus areas include Lead documentation audit activities to ensure full traceability of hygienic piping systems, Manage schedule, priorities, milestones, and deliverables, and Audit weld documentation packages for GMP and Good Documentation Practices compliance.
Important skills include Documentation Audit, GMP Compliance, Good Documentation Practices, Document Traceability, FDA cGMP Regulations, and 21 CFR Parts 210 & 211. Preferred (not required): Traceability Matrices, ALCOA+, Equipment & Utilities Installation Qualification, and EIDA.
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Full job description
Validation Project Lead / Documentation Audit 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
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Lead documentation audit activities to ensure full traceability of hygienic piping systems.
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Manage schedule, priorities, milestones, and deliverables.
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Audit weld documentation packages for GMP and Good Documentation Practices (GDP) compliance.
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Ensure document traceability.
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Coordinate resolution of documentation deficiencies and quality observations.
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Partner with Construction Management, Fabricators and Client representatives.
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Maintain validation metrics and documentation status reports.
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Mentor junior validation specialists and documentation specialists.
Required Qualifications
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Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related technical discipline (or equivalent experience).
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8+ years of pharmaceutical validation, CQV, QA, or GMP documentation experience.
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3+ years leading validation documentation or CQV teams on large pharmaceutical capital projects.
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Strong knowledge of FDA cGMP regulations (21 CFR Parts 210 & 211).
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Thorough understanding of Good Documentation Practices (GDP).
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Experience supporting Commissioning, Qualification & Validation activities.
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Experience preparing projects for client and regulatory audits.
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Excellent project management, organization, and communication skills.
Preferred Qualifications
- Experience with Traceability Matrices, ALCOA+, Equipment & Utilities Installation Qualification,
Experience with EIDA, Bluebeam, Microsoft Office and SharePoint.
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