Senior Clinical Analyst

4 days ago

Newry, United Kingdom Norbrook Full time
Job Title: Senior Clinical Analyst

Join Norbrook Laboratories Limited as a Senior Clinical Analyst and be part of a dynamic team that delivers high-quality analytical services.

About the Role

We are seeking a highly motivated and experienced Senior Clinical Analyst to join our GLP Clinical study analytical team. As a Senior Clinical Analyst, you will be responsible for conducting bioanalysis, supervising and training analytical staff, and supporting Laboratory Management to deliver project analytical phases.

Main Responsibilities
  • Perform and oversee the extraction of drug actives from biological matrices using existing analytical methods.
  • Supervise analysts within the clinical laboratories and assist in the training and development of new and existing analytical team members.
  • Conduct investigations and root cause analysis within the laboratory and identify and contribute to the assessment of deviations.
  • Oversee and/or carry out validation and maintenance tasks on laboratory equipment as required.
  • Assist in the checking and compilation of laboratory records and prepare/review/revise Standard Operating Procedures and Analytical Reports as required.
Requirements
  • A relevant Biochemistry, chemistry, biology or other applicable Science based degree.
  • A minimum of 3 years' U/HPLC experience within a GXP Laboratory environment.
  • 2 years' experience in the training and supervision of laboratory analysts.
  • Expertise in the conduct of Solvent and Solid Phase extractions (SPE) of drug actives from biological matrices.
  • 2 years' experience in Root Cause Analysis of Laboratory OOS Investigation and implementation of resulting CAPA.
  • Excellent oral & written communication skills.
  • Excellent knowledge of Microsoft Word & Excel software packages.
Desirable Criteria
  • LCMS/MS experience within a GXP Laboratory environment.
  • Expertise troubleshooting relevant laboratory equipment, HPLC, UPLC etc.
  • Experience with compiling Laboratory Documentation including Change Controls, Deviations, Risk Assessments and COSHH.

We are an equal opportunities employer and welcome applications from all sections of the community. To apply, please forward your CV via the APPLY Now button below.

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