QC Laboratory Supervisor – GMP/GLP Leader

ABBVIE; Waterford; On-site; EUR 65,000 - 82,000; Full time

Job summary

AbbVie in Waterford, Ireland, seeks a QC Pharma Supervisor to lead day-to-day Quality Control lab operations, supporting chemistry analysis and stability testing in line with schedules, regulatory requirements, and company standards.

You will supervise daily activities to ensure testing is completed accurately, on time, and compliant with GMP/GLP and related guidelines; collaborate with QA and Laboratory Management to uphold the QMS.

Qualifications

• BS in science or equivalent; Chemistry, Microbiology, or Biology preferred.
• 2-5 years of laboratory experience.
• 2-5 years of supervisory experience.
• Able to interpret laboratory data for appropriate actions.
• Identify problem areas and develop corrective actions with supervision.

Responsibilities

• Supervise daily laboratory operations and ensure compliance with regulatory requirements.
• Support scheduling and participate in Tier 1 meetings to review shift productivity.
• Ensure testing data, raw data, and results are documented accurately and on time.
• Use LIMS, Sample Manager, and Empower effectively.
• Review and interpret test results.
• Maintain Good Laboratory Practices and safe housekeeping.
• Work on a rotating monthly shift pattern.
• Collaborate with Supervisors, Quality, and Laboratory Management to ensure QMS compliance.

Skills

Problem solving

Data interpretation

Communication

Teamwork

Time management

Initiative

Analytical thinking

Leadership

Education

BS in science (Chemistry, Microbiology, or Biology)

Third-level qualification in a Science discipline

Tools

LIMS

Sample Manager

Empower

Job description

AbbVie in Waterford, Ireland, seeks a QC Pharma Supervisor to lead day-to-day Quality Control lab operations, supporting chemistry analysis and stability testing in line with schedules, regulatory requirements, and company standards.

You will supervise daily activities to ensure testing is completed accurately, on time, and compliant with GMP/GLP and related guidelines; collaborate with QA and Laboratory Management to uphold the QMS.