Senior Laboratory Analyst

3 weeks ago

Ballina, Mayo County, Ireland Charles River Laboratories Full time

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.

Job Summary

We are seeking an experienced Senior Analytical Analyst for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Analytical Supervisor and the main duties & responsibilities shall be:

  • Carrying out analytical tests using different techniques like HPLC, Capillary Electrophoresis, UV-Vis spectroscopy, Ion Chromatography, GC, and wet chemistry.
  • Practical and theoretical knowledge on several analytical techniques, with capability of troubleshooting based on the specific request.
  • Strong knowledge of GMP regulation applied to a laboratory environment.
  • Assist in developing and/or verification/validation of analytical methods that use equipment like HPLC, Ion and Gas Chromatography, spectrophotometers as well as wet chemistry techniques and compendial methods.
  • Receipt and processing of test samples in LIMS.
  • Safe and compliant disposal of all laboratories generated waste.
  • Carry out data calculations and basic statistics.
  • Assist in internal, regulatory and client visits/audits and respond to findings.
  • Sourcing, purchasing and stocking consumables, standards and reagents required for testing.

Job Qualifications

The following are minimum requirements related to the Senior Analytical Analyst position:

  • BSc/MSc. in a relevant science discipline (e.g. chemistry, biochemistry, pharmacy, and biotechnology)
  • A minimum of 3 years relevant experience in Laboratory preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO, CMO, CDMO Industry.
  • Analytical techniques (HPLC, GC, MS and similar) experience essential.
  • Experience in development and validation of analytical methods according to ICH guideline required but not essential.
  • Experience in analytical techniques/immunoassays desirable but not essential.
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