Pharmaceutical GMP QA Specialist

Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical development and testing processes. The QA Specialist will be responsible for implementing and maintaining quality management systems, conducting inspections and audits, reviewing documentation, and ensuring all activities adhere to regulatory standards, including FDA, DEA, and ISO 17025 requirements. This role requires close collaboration with the development and testing teams to maintain compliance with the regulatory requirements.

Key Responsibilities:

• Ensure adherence to pharmaceutical GMP regulations and internal quality standards.


• Conduct routine and for-cause internal audits and inspections of chemistry, microbiology, and molecular biology laboratories.


• Review and approve GMP-related documentation, including test results...