QC Analyst: Method Validation & HPLC/GC Expert

CLS - Complete Laboratory Solutions; Dublin; Vor Ort; EUR 42.000 - 52.000; Vollzeit

Zusammenfassung

Complete Laboratory Solutions (CLS) is expanding and seeking a Quality Control (QC) Analyst to join its highly regulated laboratory team. The role focuses on routine QC testing of materials, finished products and stability samples in line with approved procedures.

You will draft and review quality documentation, support method transfers and validations, and investigate deviations. Hands-on chromatography (LC-MS/MS, GC, HPLC) experience is essential, with a background in pharmaceutical drug

Qualifikationen

• Bachelor's degree in a scientific discipline.
• Minimum of 3 years' experience in a Quality Control laboratory environment.
• Experience in regulated QC setting is essential.
• Hands-on experience with chromatographic techniques including LC-MS/MS, GC, and HPLC.
• Experience in method validation, method development, and laboratory investigations.
• Pharmaceutical drug development or process development experience is desirable.

Aufgaben

• Perform routine QC testing of raw materials, intermediates, finished products, and stability samples in line with approved procedures and testing schedules.
• Draft and review quality documentation including SOPs, protocols, training modules, investigations, technical reports, and Quality Management System (QMS) documents.
• Participate in analytical method transfers, method validation activities, and method development projects as required.
• Report, investigate, and support laboratory investigations, deviations, and troubleshooting activities.
• Carry out analytical testing using techniques such as wet chemistry, GC, and HPLC, while developing proficiency in additional analytical methods.
• Support the day-to-day operation of the laboratory and contribute to continuous improvement initiatives.

Ausbildung

Bachelor's degree in a scientific discipline

Tools

LC-MS/MS

GC

HPLC

Jobbeschreibung

Complete Laboratory Solutions (CLS) is expanding and seeking a Quality Control (QC) Analyst to join its highly regulated laboratory team. The role focuses on routine QC testing of materials, finished products and stability samples in line with approved procedures.

You will draft and review quality documentation, support method transfers and validations, and investigate deviations. Hands-on chromatography (LC-MS/MS, GC, HPLC) experience is essential, with a background in pharmaceutical drug