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.
sarah.flynn@collinsmcnicholas.ie
+353 719108060