CareerShapes has partnered with a pharmaceutical client based in Dublin to recruit for a QC Analyst. The QC Analyst will be responsible for performing analytical testing of raw materials, intermediates and finished products to ensure compliance with company and GMP standards. This role plays a key part in maintaining the integrity and quality of pharmaceutical products throughout the manufacturing process.
Key Responsibilities
* Perform routine and non-routine testing of raw materials, in-process samples and finished products according to standard operating procedures.
* Operate, maintain, and troubleshoot analytical instruments such as HPLC, GC, KF, Autotitrators, IR, UV and Polarimeter.
* Accurately document all analytical data and results in accordance with GMP.
* Calibration and maintenance of laboratory equipment as required.
* Review and interpret test results, identify out-of-specification (OOS) or out-of-trend (OOT) results, and support laboratory investigations as required.
* Prepare and standardize reagents, solutions, and reference standards.
* Write and update new SOPs and test speicifications.
* Participate in method transfers, method validation, and equipment qualification activities where needed.
* Ensure laboratory compliance with cGMP, GLP, and health and safety guidelines.
* Support continuous improvement initiatives within the QC department.
Qualifications
* BSc. in Chemistry, Pharmaceutical Science, Biochemistry, or a related discipline.
* 0–3 years of experience in a GMP-regulated QC laboratory (pharmaceutical, biopharma, or related industry).
* Strong understanding of analytical chemistry principles and instrumentation (HPLC, GC, etc.).
Job Type: Full-time
Pay: From €30,000.00 per year
Work Location: In person