GMP & Documentation Specialist Quality & Compliance
Listed on 2026-10-18
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Twincraft Skincare seeks a Standards Specialist to uphold GMP and GDP practices for cosmetic and OTC products, aligning with FDA ALCOA++ data integrity principles. The role ensures manufacturing records accuracy, manages investigations, change controls, and maintains inspection-ready documentation.
Working across Quality, Manufacturing, R&D and other departments, you will drive continuous improvement, support audits, and ensure procedures meet regulatory and company standards while maintaining
Our organisation is growing, and we are hiring a GMP & Documentation Specialist for Quality & Compliance in Williston, VT, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP & Documentation Specialist for Quality & Compliance role in the description above.
We appreciate your interest in this position.
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