QC Laboratory Manager

CLS is currently going through an unprecedented and exciting period of growth and development and is looking for dynamic, dedicated and solutions driven team members, 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 and the leading provider of sampling, analysis, and analysts to the pharmaceutical, medical device, food, and environmental industries.

As well as analysis and testing at our commercial laboratories, CLS builds strategic partnerships with its clients to deliver a flexible and managed quality solution (FlexiQ) by supplying organisations with highly skilled, work-ready quality professionals on a temporary, project-specific, or long‑term basis. This service can be provided at a CLS site or directly at the client’s location.

QC Laboratory Manager

As the QC Laboratory Manager, you will lead the lab function in a state‑of‑the‑art pharmaceutical facility, ensuring high‑quality, compliant, and efficient support for manufacturing operations. You will be responsible for managing a team of analysts and overseeing all laboratory testing activities to ensure product and environmental monitoring meet regulatory and company standards.

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• Leading and managing the day‑to‑day operations of the laboratory.
  
• Coaching, mentoring, and developing the team, including performance management and training.
  
• Managing laboratory resources, including equipment qualification, maintenance, and procurement.
  
• Driving continuous improvement initiatives in lab operations, quality systems, and safety.
  
• Ensuring all testing is performed in compliance with cGMP, SOPs, and regulatory requirements.
  
• Representing the lab in cross‑functional meetings and regulatory inspections.
  
• Developing and maintaining strategies for the site, including cleanroom qualification and routine environmental monitoring.
  
• Leading laboratory investigations and implementing corrective and preventive actions (CAPAs).
  
• Ensuring adherence to the site’s safety policies and promoting a culture of safety and quality.
  

You are an experienced people manager with strong leadership qualities and a passion for quality and compliance. You thrive in a fast‑paced, regulated environment and are committed to developing your team and driving high standards. You are organized, analytical, and collaborative, with the ability to make sound decisions and influence others.

You have a degree in a related scientific discipline, along with at least 8 years’ experience in a pharmaceutical or biopharmaceutical environment, including leadership or supervisory experience.

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• Strong people management and leadership experience.
  
• Excellent communication, team management, and problem‑solving skills.
  
• In‑depth knowledge of managing processes and scheduling team activities.
  

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• A leadership role in a world‑class pharmaceutical environment.
  
• The opportunity to shape and grow a high‑performing team.
  
• Continuous professional development in a company that values innovation and quality.
  
• A collaborative and supportive culture focused on patient safety and operational excellence. xcfaprz
  
• A competitive salary.