QC Lab Analyst

Due to continued expansion this global Biotech Company seeks a QC Lab Analyst to join their GMP facility in Leinster. A global innovator and leading biopharmaceutical company that has been inventing new ground breaking treatments for numerous life threatening diseases for more than a century. Through this organisations prescription medicines, vaccines, biologic therapies, and animal health products, they work with customers and operate in more than 140 countries to deliver innovative health solutions.

The Position:

  • To Operate as part of the QC analytical team performing the allocated testing and laboratory based duties.
  • Review, approve and trend test results.
  • Peer review other analysts documentation, ensuring QC Right First Time KPIs are achieved.
  • Participate in QC daily meetings and ensure effective communication of testing progress, deviations etc.
  • Ensure that all Quality Systems within the department are adhered to on a daily basis.
  • Complete all documentation in compliance with GMP and GxP standards.
  • Participate in the laboratory aspects of OOS investigations.
  • Problem solving to get to root cause of issues.
  • Provide support with audit/inspection requirements to ensure department compliance/readiness.
  • Compliance with , Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions, including maintenance of accurate records.

The Person:

  • 2-3 years of experience in a pharmaceutical Laboratory.
  • Experienced background in Bioassay, Immunoassay and Cell Culture is essential.
  • Working knowledge of HPLC systems and software is desirable.
  • A good knowledge of cGMP, GLP, Quality Management Systems.

To find out more apply online or call Aoife Byrne at HRM +353 1 6321866.

Salary: On Application Location: Carlow