Supervisor, Laboratory Quality Control

About AbbVie

AbbVie is dedicated to discovering and delivering innovative medicines and solutions addressing serious health challenges today and the medical needs of tomorrow. Their impact spans key therapeutic fields including immunology, oncology, and neuroscience, along with products in Allergan Aesthetics.

Role Overview

As a QC Pharma Supervisor, you will lead daily Quality Control laboratory activities focused on chemistry analysis and stability testing aligned with planned schedules, regulatory standards, and company policies.

Key Responsibilities

• Manage daily laboratory operations to ensure all testing adheres to regulatory compliance.
• Assist in planning and supporting weekly and daily lab schedules; actively participate in Tier 1 meetings reviewing shift productivity.
• Ensure all test data and results are documented accurately, clearly, and timely.
• Utilize laboratory management systems including LIMS, Sample Manager, and Empower proficiently.
• Analyze and interpret laboratory test results for quality control purposes.
• Maintain compliance with safety, housekeeping, and quality standards.
• Identify and escalate discrepancies or non-conformances to leadership.
• Promote thorough housekeeping practices and uphold Good Laboratory Practices (GLP).
• Function within a rotating monthly shift schedule.
• Collaborate with supervisors, Quality Manager, and Lab Management to reinforce the Quality Management System adherence.

Qualifications and Experience

• Science degree (BSc) or equivalent qualification, with a preference for Chemistry, Microbiology, or Biology.
• Between 2 and 5 years’ experience in a laboratory setting.
• 2 to 5 years of supervisory experience.
• Proven ability to engage effectively with departmental colleagues and lab stakeholders.
• Strong problem-solving capabilities.
• Ability to interpret laboratory data implications to guide correct actions.
• Skill identifying issues needing attention from development, maintenance, production, engineering, accounting, or planning, supported by senior staff.
• Capable of communicating problems and following through corrective actions, assisting with investigations and resolutions under supervision.
• Experience operating in GMP/GLP regulated environments.
• Hands-on experience with analytical instruments including HPLC and GC, among other lab techniques.
• Working knowledge of Empower software.
• Deep understanding of laboratory data integrity principles.
• Strong communication, organization, time management, and teamwork skills.
• Ability to work autonomously and proactively.

Skills and Behaviours

• Excellent relationship building and cross-functional collaboration skills.
• High proficiency in verbal and written communication.
• Strong planning, organizational, and analytical skills.
• Decisiveness and effective problem-solving abilities.
• Adaptability and efficiency in a fast-moving environment.
• Results-oriented with a proactive, accountable mindset.
• Receptive to feedback with dedication to ongoing improvement.
• Leadership approach centered on people and aligned with AbbVie's organizational values and culture.

Additional Information

AbbVie is an equal opportunity employer committed to integrity, innovation, and community service. Applicants from veterans and persons with disabilities are encouraged.

This role requires working onsite in Westport, County Mayo, Ireland, under a rotating monthly shift scheme.