Quality Control Microbiologist

About the Role

We are seeking a skilled QC Microbiology Specialist to join a leading pharmaceutical manufacturing site located in Athlone, Co. Westmeath, Ireland. This position offers the chance to be an integral part of a GMP-regulated sterile production environment, focusing on essential quality control duties that guarantee the safety and quality of crucial medicines.

Key Responsibilities

• Carry out environmental monitoring procedures within cleanroom manufacturing zones.
• Perform comprehensive testing of water, utilities, and microbial presence, including bioburden, endotoxin analysis, total organic carbon (TOC), conductivity, growth promotion, biological indicator tests, and bacterial identification.
• Implement process and method validation protocols.
• Assist with laboratory investigations and root cause analysis utilizing structured problem-solving methods.
• Review laboratory data and ensure accuracy and compliance of GMP documentation.
• Maintain laboratory instruments and adhere strictly to GMP requirements.
• Contribute to the development and upkeep of laboratory procedures and site documentation.
• Provide training to staff on sterility assurance and microbiology awareness.
• Participate actively in media fill studies supporting sterile manufacturing qualifications.
• Raise concerns related to quality, safety, or compliance risks promptly.

Candidate Requirements

• A degree in Microbiology or related Life Sciences field.
• At least 5 years of experience within a cGMP Quality Control Microbiology laboratory setting.
• Minimum of 2 years' experience specifically in the pharmaceutical industry.
• Practical experience conducting microbiological testing in sterile manufacturing environments.
• Proficiency in environmental monitoring and utility testing techniques.
• Strong knowledge of sterility assurance principles and current GMP regulations.
• Experience with method validation and quality risk management strategies.
• Exceptional attention to detail, thorough documentation skills, and strong problem-solving abilities.

Why Join Us?

• Work in a modern, highly regulated pharmaceutical manufacturing facility.
• Collaborate with a knowledgeable Quality team dedicated to sterile manufacturing.
• Play a role in safeguarding patient health through critical quality operations.
• Engage in a supportive team environment offering continuous learning and professional growth.