Microbiologist.

Role – Microbiology & Sterilisation Specialist (12-Month Contract) Location – South County Dublin/Wicklow Salary – €65,000 (pro rata) Working week – 8.30 to 5 pm. Monday to Friday Our Client is seeking an experienced Microbiology & Sterilisation Specialist to join their team on a 12-month contract at the South Dublin/Wicklow site. This is a key technical role responsible for ensuring all products meet the highest microbiological, sterilisation, and cleanroom compliance standards within a regulated environment. Job Purpose You will provide expert oversight in microbiology and sterilisation processes, ensuring compliance with regulatory requirements, internal quality systems, and maintaining continuous inspection readiness. Key Responsibilities Maintain up-to-date knowledge of global regulatory requirements in microbiology, sterilisation (including ISO 11135 & ISO 10993), and cleanroom operations (ISO 14644).

Provide technical expertise in

Ethylene Oxide (EtO) sterilisation processes Sterilisation validation and re-qualification GLP laboratory practices Cleanroom behaviour, controls, and environmental monitoring Support Microbiology Technicians in testing, monitoring, and sterilisation activities. Define and enforce microbiological and sterilisation quality standards across the site. Ensure compliance with internal procedures and global Quality System regulations. Review sterilisation cycles and microbiological data; approve product release. Lead or support investigations into non-conformances, including root cause analysis and CAPA. Act as the site Subject Matter Expert (SME) for microbiology and sterilisation. Maintain audit and inspection readiness at all times (internal, regulatory, Notified Body). Ensure laboratory safety, equipment readiness, and data integrity compliance. Requirements Degree in Science or a related discipline, with a focus on Microbiology. Minimum 5 years’ experience in medical devices, pharmaceutical, or biotech industries.

Strong expertise in

GLP and laboratory governance Cleanroom operations and environmental monitoring Experience in process validation and cleanroom compliance. Knowledge of Ethylene Oxide sterilisation (ISO 11135) is highly desirable. Skills & Competencies Strong knowledge of ISO 13485 and FDA QSR/QMSR regulations. Excellent problem-solving and analytical skills, particularly in investigations and CAPA. Ability to work cross-functionally in a regulated environment. Strong communication and interpersonal skills. High level of proficiency in Microsoft Office. Capable of managing complex technical responsibilities independently. If you are interested in this role, send your CV to [email protected] to apply. You can also connect with Ciaran on LinkedIn or check out our other open jobs here