QC Analyst
On-site · Sligo, Connacht, Ireland
Job Summary
Maintain and perform chemical testing of raw materials and in-process samples in a GMP-regulated pharmaceutical environment. Ensure data integrity and compliance with cGMP/GLP requirements, keep up-to-date records of tests, operate and maintain test equipment (HPLC/GC), raise change requests and perform data verification, assist in training of new analysts, support transfer of new products, and help resolve quality problems while upholding EHS standards. This role requires a 3rd level Science qualification and prior hands-on experience with HPLC or GC in a pharmaceutical manufacturing setting. The position is a 12-month fixed-term contract with rotating shifts.
Required Qualifications
- 3rd level qualification in a relevant Science discipline
- Minimum of 6 months of experience in HPLC or GC
- Experience operating to cGMP standards utilizing laboratory equipment
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