Standards Specialist

The Standards Specialist supports Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP), including the FDA’s ALCOA++ data integrity principles, for cosmetic and OTC drug-cosmetic products manufactured by Twincraft Skincare. The role manages and verifies manufacturing records, investigations, and change controls; supports audits; and maintains accurate, current, inspection-ready records. Working across Quality, Manufacturing, R&D, and other departments, the specialist drives continuous improvement and ensures activities meet applicable procedures, regulatory requirements, customer expectations, and company standards.

• Maintain and support GMP documentation systems, ensuring accuracy, completeness, traceability, and compliance with regulatory standards.
• Lead and support investigations of deviation, non-conformance, and out-of-specification results.
• Perform root cause analysis and support development of corrective and preventive actions (CAPA) as appropriate.
• Manage compliance records and workflows within ETQ (or equivalent Quality Management System (QMS) platform).
• Support the creation, revision, and lifecycle management of Standard Operating Procedures (SOPs).
• Support training program administration, including tracking, documentation, and coordination of GMP and compliance training.
• Support internal and external audits, including preparation, documentation retrieval, and follow-up on findings.
• Conduct and support laboratory investigations related to quality or compliance issues.
• Identify and drive continuous improvement initiatives across quality and compliance processes.
• Support change control processes, ensuring proper documentation and cross-functional review.
• Maintain document management systems, ensuring version control, retention, and accessibility of controlled documents.
• Identify unusual trends, non-conformances, or other potential concerns and escalation them to the appropriate personnel.
• Support company adherence to policies and procedures, practices associated with held certifications and regulatory commitments.
• Maintain accurate, timely, and complete documentation and data associated with assigned responsibilities.
• Communicate compliance, quality, and documentation concerns promptly and objectively.
• Support operational flexibility and changing business needs at Twincraft without compromising product quality, compliance, or data integrity.
• Work cross functionally with all departments within Twincraft.
• Support and adhere to Twincraft's policies, procedures, and values.
• Perform other duties as assigned.