Our client, a leading biopharmaceutical company, is keen to hire a QC Micro Analyst to join their team on an initial 12-month contract in Sligo.Responsibilities of a QC Micro Analyst (Full job description available on request):
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.
Ideal background:
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.
Note: This role is 100% onsite and includes a shift.One week of days; 07:00-15:30 (Mon-Fri) followed by a week of evening shift; 15:00-23:30 (Mon-Fri).The weeks rotate: one week of days, one week of evenings.For a confidential discussion and more information on this QC Micro Analyst role, please contact Sarah Flynn.+353 719108060
