A global, research-based biopharmaceutical company is keen to hire a QC Micro Analyst to join their site in Sligo. This is an initial 18-month contract and is a full-time on-site position. Hours of work include one week of days followed by a week of evening shift.
Responsibilities: Maintain and align with Laboratory Documentation and Computerized Systems Data Integrity requirements.Understand Regulations and business processes required to maintain Laboratory Data Integrity.Carry out environmental and microbiological tests as required.Define and update procedures for the plant relative to microbiological and environmental testing.Complete validation of equipment and test methods for microbiological tests.Test method transfer of microbiological methods.Develop microbiological laboratory procedures.Maintain up-to-date and detailed records of all tests performed.Education and Experience: Third level qualification in microbiology required or equivalent science discipline.A good knowledge of aseptic processes' manipulation together with experience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelines.Lab experience within industry – Bioburden / Endotoxin / Growth Promotion / Environmental Monitoring.Experience within a sterile cleanroom environment.For a confidential discussion and more information on the role, please contact Sarah Flynn at ****** or +353 719108060.
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