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General Electric QC Equipment Specialist - Fixed term 18 months in Cork, Ireland

Job Description Summary

As a QC Specialist, you'll be responsible for providing QC analytical laboratory equipment (Chemistry and Micro), software systems and CPV/Trending support within imaging contrast media in the QC Laboratory, in GEHC PDx, Cork and for ensuring that Laboratory activities and requirements (as required) are fulfilled for its operation

Job Description


  • Annual Contracts –Negotiate contract price, raise PO’s and maintain files.

  • Compliance Monthly/Quarterly tasks as per relevant Instrument Admin SOP’s.

  • PM Scheduling as per Maximo, Liaise with vendors when scheduling dates, completing inductions and ensuring safe permit is up to date before vendor.

  • Documenting/ Completing all PM’s on Maximo and master equipment file.

  • Equipment troubleshooting on request. Ad hoc vendor site visits for equipment repairs – complete resulting Maximo paperwork.

  • review and closure of Maximo records/Paperwork for other team members (Micro/Chem/Equipment Validation).

  • Equipment associated IR’s and Investigations.

  • Setup of new users on QC Equipment, remove redundant users. Password resets on request.

  • Provide training support for new starts

  • Lab system admin for QC Chemistry Equipment. Audit trail reviewer.

  • Annual Periodic reviews of QC Chemistry systems.

  • Complete review/approval of validation documentation for other team members on request.

  • Data Integrity Projects on request in conjunction with specialist team.

  • QA Agreements for all vendors.

  • Provide training support for new starts

  • Manual daily backups as required

  • CPV or Continuous Process Verification Support – trending of analytical data to support process analysis and oversight

  • Review industry and regulatory standards & guidelines to ensure equipment is installed, qualified to current standards.

  • Audit support for equipment-related preparation and response

Qualifications and experience

  • Degree (or equivalent) in Chemistry / Microbiology, or in a Science/Engineering subject

  • Familiar with Regulatory and ICH expectations of good laboratory practices, equipment qualification and maintenance.

  • Strong theoretical and practical knowledge of equipment qualification and maintenance.

  • Experienced in data compilation, review and report generation

  • Project Management - leading & oversight as well as contributory role

Desirable skills

  • Works in an organized manner

  • Works independently and seeks solutions

  • Clear thinker and disposed for troubleshooting

  • Good understanding of how work of own team integrates with other teams

  • Contributes when working in cross functional groups

  • Maintains a latitude to rearrange the sequence to complete task/duties based on changing work situations

Eligibility requirements

  • A good level of English and an EU Work Permit

Inclusion and Diversity

GE Healthcare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

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Additional Information

Relocation Assistance Provided: No