Senior QC Analyst

AbbVie

Sligo, Ireland

Job Description

We are looking for a Senior QC Analyst , at our Manorhamilton Rd site in Sligo.

Responsibilities:

  • Ensure Laboratory Documentation and Computerized Systems compliance with Data Integrity policies and regulatory requirements.
  • Understand Regulations and business processes required to maintain Laboratory Data Integrity.
  • Ensuring timely completion of all laboratory analysis assigned to shift.
  • Ensuring that analysts working in the assigned cell or team are performing to the best of their ability, coaching and providing guidance where issues occur such as poor set-up or test execution performance.
  • Improving the overall efficiency and velocity within the assigned team.
  • identifying and implementing improvements in analytical practices using ‘Zero, Believe it, Achieve it’
  • Ensuring that the agreed test schedule is adhered to and identifying recovery paths to bring test schedules back into alignment with plant requirements.
  • Identifying weaknesses in laboratory performance and working with the laboratory Supervisors to rectify.
  • Supporting & initiating analytical OOS issues as they arise in a timely manner both through practical work and through Soltraqs.
  • Acting as designee for the Laboratory Supervisor as assigned.
  • Ensuring 6S excellence is maintained across the Laboratory.
  • Instilling a quality culture of Zero, Believe it, Achieve it amongst the QC laboratory team
  • Ensuring that all laboratory test equipment is utilised and maintained correctly.
  • Executing and/or supporting projects through the Lab Management team.
  • Maintaining up-to-date, complete and precise records of all tests performed.
  • Acting as the primary point of contact for any analytical issues which arise.
  • Developing expertise and understanding of current and future analytical techniques.
  • Developing and changing of in-house laboratory procedures as appropriate.

Qualifications

  • 3rd level qualification in a relevant Science discipline.
  • Minimum 3 years analytical experience in the pharmaceutical industry.
  • Proven track record in an analytical role. Must be expert in HPLC, GC,LCMS, GCMS,
  • Automatic titration, Identification techniques.
  • Strong knowledge on regulatory requirements.
  • Proficient in using analytical equipment in the QC lab.

Don't forget to mention EuroPharmaJobs when applying.

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