IN-VITRO SENIOR TECHNICAL ANALYSTMAYO

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ICDS RECRUITMENT

  • 24 UPPER FITZWILLIAM STREET
  • DUBLIN 2
  • Job reference number:15450990
  • Client ID:RI/SF16815
  • Posted on:12-JUN-2019
  • Salary:NEGOTIABLE
  • Location:MAYO
  • Job type:PERMANENT

Benefits: CAR PARKING, PAID HOLIDAYS, PENSION / PRSA

In-Vitro Senior Technical Analyst - Mayo

Key Purpose

Our Client is looking to recruit a Senior Technical Analyst to work in their In-Vitro (AVA) Laboratory to complete the establishment of a new suite of laboratories within a specific timeframe and to manage the laboratory once established and fully operational. The role will report to the Biosafety & Bioassay Development Manager

Key Responsibilities

  • Qualification and/or validation of all equipment for new AVA & Mycoplasma Laboratories in accordance with GMP and corporate validation requirement standards and guidelines.
  • Draw up cell banking and virus stock SOPs and implement testing in strict accordance with SOP(s) ensuring full GMP regulatory compliance as appropriate.
  • Finish qualification of all cell banks for use in AVA and Mycoplasma testing.
  • Establishment of Test Method SOPs and validation of methods.
  • Complete understanding off all regulatory guidelines.
  • Generation of GMP compliant SOPs, Protocols and reports.
  • Carrying out test method procedures.
  • Liaise with the Quality Department for the generation of all departmental quality documents including audit responses, facility replies and deviation reports.
  • Assist in laboratory investigations where necessary.
  • Responsible for reporting progress information to Management.
  • Provide technical training to team as required.
  • Update current standard operating procedures.
  • Generate risk assessments for laboratory and test items as required.

Qualifications & Experience .

  • BSc or MSc a relevant science discipline (e.g. Virology)
  • A minimum of 3 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry.
  • Experience in in-vitro bioassays and project management highly desirable.
  • Experience in virology and biosafety testing requirements highly desirable.
  • In-Vitro Analytical techniques essential.
  • Knowledge of biosafety classifications and Code of Practice for the Safety, Health and Welfare at Work (Biological Agents) Regulations 2013 (S.I. No. 572 of 2013) desirable.
  • Ability to problem solve and work on own initiative.

This job originally appeared on RecruitIreland.com