QC Pharma SupervisorAbbVie 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 RoleAs 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 ResponsibilitiesSupervise 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.QualificationsBS in science or equivalent (Chemistry, Microbiology, or Biology preferred)2-5 years of laboratory experience2-5 years of supervisory experienceDemonstrated skills to deal effectively with members of the department and the areas serviced by the laboratoryProblem solving skills are requiredMust be able to interpret impact of laboratory data for appropriate and effective actionsMust be able to identify problem areas requiring development, maintenance, production, engineering, accounting, or planning with assistance from more senior staffMust 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 resolutionAdditional InformationThird-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.Strong relationship-building skills and the ability to work effectively across functions.Excellent verbal and written communication skills.Strong planning, organizing, 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.US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: Fraud AlertWe have recently become aware of various recruitment phishing scams targeting job seekers. Please be advised:AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.Protect yourself by verifying job offers and communications. Your safety is important to us.Pay Range: $-Where We WorkRole is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.