R&D Project Associate-Lab Systems - Waterford, Ireland - Teva Pharmaceuticals

    Teva Pharmaceuticals
    Teva Pharmaceuticals Waterford, Ireland

    2 weeks ago

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    Description

    Who we are

    We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us.

    We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.

    We are inviting applications for the role of R&D Project Associate. This is a 12 Month FTC role and offers the opportunity to be involved in all different aspects within the Lab and to operate in a diverse and changing environment.

    A day in the life of our Project Associate – Laboratory Systems

  • Providing a Calibration and/or Maintenance Service to the R&D laboratory that includes instrumentation calibrations, scheduling and tracking of instrument maintenance and instrument lifecycle management.
  • Review and approve analytical instrumentation qualification, calibration, repairs and documentation.
  • Ensure instrument maintenance and verification is appropriate to the use of the instrument
  • Manage all instrument specific investigations such as calibration deviations
  • Participate in new instrument purchase and qualification
  • Participate as part of a team of R&D Specialists, QA validation Specialists and Computer System Validation personnel to deliver on the qualification of new instruments.
  • Liaise with sister sites and vendors on instrumentation purchase, qualification and lifecycle management.
  • Ensure compliance with corporate policies, directives and current regulatory requirements for laboratory instrument qualification, calibration and lifecycle management.
  • Participate in definition and establishment of instrument related procedures.
  • Participate in troubleshooting complex instrumentation issues.
  • Who we are looking for

    Are you....

  • Educated to Degree Level preferably in Science, Computer Science, Life Sciences or a related field
  • Do you have....

  • Experience working in a highly regulated environment within the pharmaceutical laboratory environment
  • Knowledge and experience of cGMP and its implementation to laboratory instrumentation and laboratory processes
  • Excellent verbal and written English communication skills.
  • Knowledge of Pertinent SOPs related to analytical instrumentation qualification and computer system development life cycle.
  • Knowledge of Data Integrity principals as they related to regulatory rules, regulation and guidelines.
  • Knowledge of FDA, CGMP, and SOP regulatory rules, regulation and guidelines.
  • Knowledge of Business, scientific and personal computer hardware and software applications.
  • Knowledge of Current Company policies, practices and procedures, including safety rules and regulation.