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.

Roles and Responsibilities

• Working as directed by Microbiology Lab Supervisor according to company safety policies and cGMP.

• Perform microbiological testing including PET, Endotoxin, Pharmaceutical Product Testing, and other assigned tasks.

• Support the setup of new client testing requirements and specifications; contribute to the generation of new test methods and method transfers.

• Participate in validation activities, including Biological Indicator (BI) studies and cleaning verification.

• Adherence to GMP and GDP.

• Data entry of test results into LIMS system.

• Record results promptly, ensuring accuracy and compliance with procedures.

• Conduct and assist with investigations of out-of-specification (OOS) results, ensuring adherence to site procedures.

• Complete all testing documentation and LIMS entries, ensuring Right First Time (RFT) KPIs are met.

• Manage stock control and maintain adequate supplies within the Microbiology Laboratory.

• Generate, update, and maintain laboratory documentation as required.

• Contribute to the Lean Laboratory program within the Microbiology Laboratory. Qualifications:

• 3rd level qualification in microbiology or a science related discipline

• 1-2 years’ experience. Endotoxin experience desired.

• Strong communication skills, both verbal and written.

• Effective team player with excellent organizational and documentation skills.

• Ability to work accurately, efficiently, and compliantly in a dynamic, progressive environment.

• Strong knowledge of microbiological aspects of GMP for pharmaceutical and medical devices

• Good knowledge of GMP Standards and FDA requirements