Quality Control (QC) Analyst

Complete Laboratory Solutions; Dublin; On-site; EUR 42,000 - 52,000; Full time

Job summary

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

Qualifications

• 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.

Responsibilities

• 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.

Education

Bachelor's degree in a scientific discipline

Tools

LC-MS/MS

GC

HPLC

Job description

Quality Control (QC) Analyst

Overview

CLS is currently going through an unprecedented and exciting period of growth and development and is looking for dedicated, solutions driven team members with a flexible approach, who want to be part of the company’s continued success.

Founded in 1994, Complete Laboratory Solutions (CLS) is the highest accredited contract laboratory in Ireland, providing industry-leading sampling and analysis; and fully trained micro and analytical analysts on contract to clients in the food, environmental, medical device, biopharmaceutical, and pharmaceutical sectors.

We offer bespoke managed service solutions that give clients the option of having our expert team on-site at their own facility or outsourcing those services to us here at CLS.

Key Responsibilities

• 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, Gas Chromatography (GC), and High-Performance Liquid Chromatography (HPLC), while developing proficiency in additional analytical methods.

• Support the day-to-day operation of the laboratory and contribute to continuous improvement initiatives.

Requirements

Education & Experience

• Bachelor's degree (BSc) in a scientific discipline or related field.

• Minimum of 3 years' experience in a Quality Control laboratory environment.

• Previous experience within a 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.

Diversity, Equity & Inclusion

Complete Laboratory Solutions (CLS) is committed to creating a diverse, inclusive, and equal workplace where everyone is treated with respect and given the opportunity to succeed. We are proud to be an Equal Opportunities Employer and welcome applications from all qualified candidates regardless of background, gender, age, disability, ethnicity, religion, sexual orientation, or any other protected characteristic.