Method Development and Validation Analyst | Mayo, Ireland

  • Leading Pharma Company in the West of Ireland
  • Excellent career progression opportunities along with a generous package.

We are presently seeking interest for the role of Method Validation Analyst for our clients Analytical Department based in Mayo. This role shall report to the Method Development & Validation Supervisor.

Main Duties and Responsibilities:

  • Carry out analytical methods i.e. chromatographic, UV, CE-SDS, icIEF and/or ELISA as part of method development, validation or troubleshooting.
  • Work with Projects Leader to provide results/outcome of the testing.
  • Assist in generating SOPs.
  • Sourcing, purchasing and stocking consumables, standards and reagents required for testing.
  • Searching scientific literature.
  • Receipt and processing of test samples in LIMS
  • Carry out data calculations, basic statistics and trending.
  • Provide additional information at the clients request as required.
  • Assist in internal, regulatory and client visits/audits and respond to findings.
  • Safe and compliant disposal of all laboratory generated waste.

The following are minimum requirements related to the Method Development and Validation Analyst position:

  • 1-2 years’ relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry.
  • Experience in method development and validation essential.
  • Minimum B.Sc. in a relevant science discipline (e.g. Analytical Chemistry)
  • Experience in analytical techniques/immunoassays desirable.

For more information about this position contact on +353 1 687 7188.
To apply at the above position, send your CV to putting “Method Development and Validation Analyst ” in email’s title.