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QC Lab Supervisor Days

AbbVie


Job Location:

Sligo - Ireland

Monthly Salary: Not provided by the employer
Posted: 1 September 2026 (5 days ago)
Application Deadline: 29 November 2026
Vacancies: 1 Vacancy

Job Summary

AbbVie is seeking an experienced QC Supervisor to lead a team of laboratory analysts within our Quality Control function in Sligo. This role is responsible for ensuring that raw materials in-process samples finished products stability studies and contract testing activities are completed to the highest quality standards on schedule and in compliance with GMP and regulatory requirements.

As QC Supervisor you will provide leadership and coaching to a team of 2-12 analysts driving laboratory performance data integrity compliance and continuous improvement initiatives. You will oversee day-to-day laboratory operations support investigations ensure equipment and systems compliance and collaborate cross-functionally with Manufacturing Quality Assurance and Supply Chain teams.

Key Responsibilities

  • Lead coach and develop a team of QC analysts to drive performance and quality excellence.
  • Ensure compliance with GMP Data Integrity HPRA/FDA and internal quality requirements.
  • Oversee laboratory testing activities and ensure adherence to testing schedules.
  • Drive continuous improvement Right First Time (RFT) and operational excellence initiatives.
  • Lead analytical investigations OOS/OOT events root cause analysis and CAPA activities.
  • Support laboratory inspections audits product transfers and project work.
  • Maintain laboratory documentation procedures training records and equipment compliance.
  • Act as a subject matter expert for analytical testing and laboratory operations.

Qualifications :

  • Bachelors degree in Analytical Chemistry or a related scientific discipline.
  • Minimum 4 years analytical laboratory experience within the pharmaceutical industry.
  • Strong hands-on expertise in analytical techniques including HPLC GC LCMS GCMS titration and identification methods.
  • Experience working in a GMP-regulated environment with strong knowledge of regulatory requirements and data integrity principles.
  • Previous leadership supervisory mentoring or team coaching experience.
  • Experience supporting product or method transfers is an advantage.

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No


Employment Type :

Full-time


About Company

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AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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