Detail

Salary
negotiable
Location
Ballina, County Mayo, Ireland
Posted by: Charles River
22 Dec
54 Views
20 Feb expires

In-Vitro Analyst

Ballina, County Mayo, Ireland
Job Description

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

 

We are seeking an In Vitro (Cell Culture/Virology) Analyst to work in and help establish a new Cell Culture and Virology Laboratory located in Ballina, Co. Mayo, Ireland.

 

This role shall report to the In-Vitro (Cell Culture/Virology) Supervisor and the main duties & responsibilities shall be to assist the Department Manager in the following:

 

  • Qualification and/or validation of all equipment for the new Cell Culture and Virology Laboratory in accordance with GMP and corporate validation requirement standards and guidelines.
  • Draw up SOPs and implement testing in strict accordance with these SOP(s) ensuring full GMP regulatory compliance as appropriate.
  • Generate and Qualify cell banks for use in client specific testing.
  • Establishment of Test Method SOPs and validation of methods, where appropriate.
     
    Core duties shall include:
     
  • Complete understanding off all regulatory guidelines.
  • Executions of Protocols and reports.
  • Carrying out test method procedures.
  • Assist the Department Manager and/or Supervisor in addressing all departmental quality documents including audit responses, facility replies and deviation reports.
  • Assist in laboratory investigations where necessary.
  • Participate in training as required.
  • Update current standard operating procedures, if required.
  • Assist in generation of risk assessments for laboratory and test items as required.
     
Job ID Reference
1463
Desired Skills & Experience
  • BSc in a relevant science discipline (e.g. Biology, Biochemistry, etc.)
  • A minimum of 1 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry is highly desirable.
  • 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.
Company
  Boston, MA, USA
For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
  Workplace
 Ballina, County Mayo, Ireland