QA/RA Specialist - Pharmaceutical GLP/GMP Experience

QA/RA Specialist - Pharmaceutical GLP/GMP Experience

Synergy is seeking a knowledgeable and meticulous QA/RA Specialist with strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical industry. The specialist will be responsible for supporting the implementation, maintenance, and continuous improvement of quality and regulatory compliance systems to ensure adherence to FDA, EMA, and other regulatory requirements. This role involves reviewing procedures, ensuring documentation compliance, conducting internal audits, and assisting with regulatory submissions and inspections.

Key Responsibilities:

• Develop, review, and maintain quality assurance and regulatory affairs documentation in compliance with GLP and GMP standards.


• Ensure adherence to regulatory requirements from FDA, EMA, and other global regulatory agencies.


• Conduct internal audits and inspections to assess ...