Darbo aprašymas

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.

• 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 client's request as required.
• Assist in internal, regulatory and client visits/audits and respond to findings.
• Safe and compliant disposal of all laboratory-generated waste.

Reikalavimai

• 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.

Įmonė siūlo

• All social guarantees legal work in Ireland/Europe


• Simple recruitment process (all documentation sign online)


• Accommodation provided, close to the workplace and transport to/from work


• Health insurance for health care;


• Timely and fair remuneration


• Company car


• Opportunity to gain extensive international experience and further professional development


• Leading Pharma Company in the West of Ireland


• Excellent career progression opportunities along with a generous package.