Supervisor, Laboratory Quality Control

QC Pharma Supervisor

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 escalate 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.
• 12 years experience working as an Analyst in a GMP/GLP environment.
• 12 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 AbbVies 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. 

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