Job Title: QC Analyst
Location: Arklow, County Wicklow
Industry: Pharmaceutical
Job Type: Full-time / Permanent
About the Role
Our client, a leading pharmaceutical organisation based in Arklow, Co. Wicklow, is seeking an experienced and detail-oriented Quality Control (QC) Analyst to join their team. The QC Analyst will play a critical role in ensuring that all raw materials, in-process samples, and finished products meet quality and regulatory standards through rigorous testing and documentation.
Key Responsibilities
1. Conduct chemical and physical testing of pharmaceutical raw materials, intermediates, and finished products in accordance with established methods and SOPs.
2. Perform analytical testing using a range of techniques including, but not limited to:
3. High-Performance Liquid Chromatography (HPLC)
4. Wet Chemistry techniques
5. Dissolution Testing
6. Accurately record, review, and report analytical results in compliance with GMP and data integrity requirements.
7. Ensure all work is completed in compliance with cGMP, SOPs, and regulatory guidelines.
8. Participate in method development, transfer, and validation activities as required.
9. Support investigation of non-conformances, out-of-specification (OOS) results, and deviations.
10. Assist in equipment calibration, troubleshooting, and maintenance.
11. Maintain and manage laboratory documentation and electronic systems effectively.
12. Participate in internal and external audits, providing data and technical support as needed.
13. Contribute to continuous improvement initiatives in the laboratory.
14. Adhere to all health, safety, and environmental (HSE) standards and policies.
15. Provide support for training and mentoring of junior analysts, where applicable.
Key Requirements
1. Degree in a scientific discipline such as Chemistry, Pharmaceutical Science, Biochemistry, or a related field (food science not applicable).
2. 2–5 years of experience in a Quality Control or analytical laboratory role within the pharmaceutical industry.
3. Proven hands-on experience with HPLC, Wet Chemistry, and Dissolution testing.
4. Strong understanding of GMP and regulatory compliance.
5. High attention to detail with strong analytical and problem-solving skills.
6. Proficient in technical writing and documentation practices.
7. Effective communication skills and the ability to work independently or as part of a team.
What’s on Offer
1. Opportunity to work in a growing, dynamic, and highly regulated environment.
2. Career development opportunities within a leading pharmaceutical organisation.
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