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Job Description
A QC Micro Analyst is required for a full-time, shift role on an initial 12-month contract with a multinational biopharmaceutical client in Cork.
The successful candidate will be responsible for carrying out tasks and projects related to raw material, utility, in-process, release, and stability testing of biotechnology products as required by Good Manufacturing Practice (GMP).
Key Responsibilities:
- Achieve a high level of competency in laboratory methods and procedures to support raw material, utility, in-process, release, and stability testing of biotechnology products.
- Perform routine and non-routine Microbiological and/or Biochemical/Chemical testing activities as required.
- Ensure that all testing is completed, reviewed, and approved within agreed turnaround times.
- Ensure QC activities are carried out in compliance with product license commitments, cGMP, and company quality standards.
Requirements:
- Bachelor's Degree (Level 8) in Science or related Technical discipline.
- A minimum of 2 years' experience in a QC laboratory-testing environment within the biological and/or pharmaceutical industry.
- Demonstrated knowledge and testing experience in an FDA/HPRA-approved QC laboratory, including Cell Culture Based Bioactivity Testing, Endotoxin, Bioburden.
About the Company:
Career Wise Recruitment is a specialist recruitment agency established in 1999, providing career opportunities in the life sciences, ICT, engineering, food, and agri sectors.
Skills: QC Analyst, Microbiology