Job Description
A QC Micro Analyst is required for a 12-month contract in Cork. The role involves microbiological, chemistry, and biochemistry testing, with a focus on Bulk API and final drug product. The candidate must have superior technical knowledge and experience in IMB/FDA regulated facilities. Responsibilities include rapid turnaround of samples, data review, and approval, as well as providing support and advice to manufacturing. The ideal candidate will have specific testing experience in bioburden, endotoxin, and sterility testing, and will be knowledgeable of FDA/EMEA regulatory requirements. A BSc (Honors) in a scientific discipline is required, along with a minimum of 2 years experience in the Pharmaceutical Industry. Interested candidates should submit an updated CV with relevant experience in microbiology, endotoxin, bioburden, and environmental monitoring.