Opportunity Summary: We are seeking a skilled Quality Assurance Associate to join our team in the pharmaceutical industry. This is an excellent opportunity for individuals with a strong background in quality assurance and laboratory support. Job Description: The successful candidate will be responsible for ensuring compliance with GMP regulations. Key responsibilities include approving quality-related documents, reviewing and approving GMP standard operating procedures, raw material specifications, sampling protocols, master formulas, process flow documents, qualification and validation documents, including IQ/OQ/PQ & validation documents for facility, equipment, computer systems, GMP utilities, analytical methods, and processes, stability data, sampling protocols, and Annual Product Reviews. Requirements: * Bachelor's/Master's/PhD degree in Chemistry, Microbiology, Biochemistry, Biotechnology or a Science related subject * Minimum of two year's experience in lab support from a QA standpoint About the Role: This is an exciting opportunity for a motivated individual to develop their skills in quality assurance and laboratory support. The ideal candidate will have a strong understanding of GMP regulations and laboratory practices. Key Responsibilities: