QC Lab Lead, Pharma Quality & Compliance

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 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.