Supervisor, Laboratory Quality Control

AbbVie; Westport; On-site; EUR 55,000 - 75,000; Full time

Job summary

AbbVie is seeking a QC Pharma Supervisor to lead day-to-day Quality Control laboratory operations, supporting chemistry analysis and stability testing in line with defined schedules, regulatory requirements, and company standards.

You will supervise daily laboratory activities, participate in Tier 1 meetings, and collaborate with Supervisors, Quality, and Laboratory Management to uphold the Quality Management System.

Qualifications

• BS in science or equivalent (Chemistry, Microbiology, or Biology preferred).
• 1–2 years’ experience working as an Analyst in a GMP/GLP environment.
• 1–2 years’ experience working with analytical equipment, particularly HPLC and GC, as well as other laboratory techniques.
• Working knowledge and experience using Empower.
• Strong understanding of Data Integrity from a laboratory perspective.

Responsibilities

• Supervise daily laboratory operations and ensure team activities are carried out in compliance with regulatory requirements.

Skills

Relationship-building

Communication

Planning & organizing

Analytical skills

Problem-solving

Leadership

Teamwork

Initiative

Education

Bachelor's degree in Chemistry, Microbiology, or Biology

Third-level qualification in a Science discipline, preferably Chemistry

Tools

LIMS

Sample Manager

Empower

HPLC

GC

Job description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com . Follow @abbvie onLinkedIn, Facebook ,Instagram ,X andYouTube.

Job Description

AbbVie is seeking a QC Pharma Supervisor to lead day-to-day Quality Control laboratory operations, supporting chemistry analysis and stability testing in line with defined schedules, regulatory requirements, and company standards.

About the Role
As QC Pharma Supervisor, you will supervise daily laboratory activities to ensure testing is completed accurately, on time, and in compliance with GMP/GLP and other applicable regulatory guidelines. You will support scheduling, participate in daily Tier 1 meetings, and work closely with Supervisors, Quality, and Laboratory Management to uphold the Quality Management System.

Key Responsibilities

• Supervise daily laboratory operations and ensure team activities are carried out in compliance with regulatory requirements.
• Support weekly and daily laboratory schedules and participate in daily Tier 1 meetings to review shift productivity.
• Ensure all testing data, raw data, and results are documented accurately, legibly, and on time.
• Use laboratory systems such as LIMS, Sample Manager, and Empower effectively.
• Review and interpret test results.
• Promote and maintain compliance with company standards in safety, housekeeping, and quality.
• Identify and elevate any discrepancies or non-conformances to management.
• Ensure good housekeeping and adherence to Good Laboratory Practices.
• Work on a rotating monthly shift pattern.
• Collaborate with team members, Supervisors, the Quality Manager, and the Laboratory Manager to ensure compliance with the Quality Management System.

Qualifications

• BS in science or equivalent (Chemistry, Microbiology, or Biology preferred)
• 2-5 years of laboratory experience
• 2-5 years of supervisory experience
• Demonstrated skills to deal effectively with members of the department and the areas serviced by the laboratory
• Problem solving skills are required
• Must be able to interpret impact of laboratory data for appropriate and effective actions
• Must be able to identify problem areas requiring development, maintenance, production, engineering, accounting, or planning with assistance from more senior staff
• Must also be able to identify, communicate, and follow-through to completion and assist in the development of necessary corrective action plans to resolve the problem with supervision. May also assist in the activities required for the investigation and resolution

Additional Information

Qualifications and Experience

• Third-level qualification in a Science discipline, preferably Chemistry.
• 1–2 years’ experience working as an Analyst in a GMP/GLP environment.
• 1–2 years’ experience working with analytical equipment, particularly HPLC and GC, as well as other laboratory techniques.
• Working knowledge and experience using Empower.
• Strong understanding of Data Integrity from a laboratory perspective.
• Excellent communication, organization, time management, and teamwork skills.
• Demonstrated ability to work independently and take initiative.

Skills and Behaviours

• Strong relationship-building skills and the ability to work effectively across functions.
• Excellent verbal and written communication skills.
• Strong planning, organising, and analytical skills.
• Sound decision-making and problem-solving ability.
• Adaptable and effective in a fast-paced, dynamic environment.
• Results-driven, with a proactive and accountable approach.
• Open to feedback and committed to continuous improvement.
• A people-centered leadership style aligned with AbbVie’s values and culture.

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.