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Senior Molecular Biology Analyst

Job Seekers Ireland Science Pharmaceutical

Job Summary

  • Mayo
  • Permanent
  • BBBH771155
  • Dec 01, 2020
  • Competitive
Job Description

Excellent opportunity to join a Mayo based bio lab to work in and establish new PCR Laboratories. Excellent opportunity to grow and develop in a new environment.

This role shall report to the Molecular Biology Supervisor and the main duties & responsibilities shall be to assist the Supervisor and Department Manager in the following:

  • Qualification and/or validation of all equipment for new PCR Laboratories in accordance with GMP and corporate validation requirement standards and guidelines.
  • Draw up SOPs and implement testing in strict accordance with SOP(s) ensuring full GMP regulatory compliance as appropriate.
  • Interpret data and troubleshoot assays.
  • Participate in the validation and qualification of molecular assays.

    Core duties shall include:

  • Complete understanding off all regulatory guidelines.
  • Generation of GMP compliant SOPs, Protocols and reports.
  • Perform laboratory activities necessary for molecular biology testing including but not limited to reagent preparation, laboratory maintenance, generation of routine GMP reports and routine testing of client samples.
  • 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.

    The following are minimum requirements related to the Senior Molecular Biology Analyst position.

  • BSc or MSc a relevant science discipline (e.g. Molecular Biology)
  • 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 molecular biology techniques, especially PCR and Q-PCR and project management essential.
  • Experience in establishment and validation of molecular biology methods is highly desirable.
  • 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.

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.

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Consultant Details

Consultant Details

julieann-fitzpatrick
Julieann Fitzpatrick
  • Senior Consultant
  • 353 (0) 21 2300300
  • jfitzpatrick@morganmckinley.com