We are seeking an experienced Senior Analytical Analyst for one of our key clients Biologics
Division located in 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

Job Type: Full-time

Benefits:

• Private medical insurance

Schedule:

• Monday to Friday

Application question(s):

• 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.

Location:

• CO. Mayo (required)

Work Location: In person
Reference ID: 23042

• 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