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Clinical Laboratory Manager
Tipp City, OH

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Abbott Laboratories

Quality Control Analytical Laboratory Supervisor - Pharmaceutical

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Job Description

Quality Control Analytical Laboratory Supervisor -
Pharmaceutical Date Posted:
11 October 2026
Closing Date:
November 10, 2026
Recruiter:
Abbott Laboratories Location:
Tipp City, Ohio Salary:
USD104,000
to
USD138,000
Job Type & Industry:
Healthcare & Pharmaceutical Contract Type:
Permanent Job Reference:
3017382217-2 Apply for this job now Job Description Abbott Laboratories seeks an Analytical Laboratory Supervisor to lead a team supporting biotech and pharmaceutical product testing. In this role, you will oversee routine and complex analytical testing for raw materials, in-process samples, and finished products, ensuring accuracy, data integrity, and regulatory compliance. You will manage workflows, mentor analysts, troubleshoot instrumentation, and drive continuous improvement in methods and processes. Partner cross functionally with QA, Manufacturing, and R D to support product release, investigations, and method transfers. Contribute to Abbott's mission-driven culture and enjoy robust development opportunities in a global organization. Responsibilities Supervise day-to-day operations of the analytical laboratory and coordinate testing priorities. Oversee execution and review of analytical tests for raw materials, in-process, and finished products under GMP. Ensure data integrity, documentation accuracy, and compliance with FDA, ICH, and internal quality standards. Lead, coach, and develop laboratory staff through training, performance feedback, and mentoring. Troubleshoot analytical methods and instrumentation (e.g., HPLC, GC, MS) to resolve technical issues. Manage method validation, verification, and transfer activities in collaboration with QA and R D. Implement and monitor lab safety practices, housekeeping, and preventive maintenance programs. Drive continuous improvement in workflows, turnaround times, and analytical capabilities. Collaborate cross-functionally with Manufacturing, QA, and R D to support product release and investigations. Prepare for and support internal and external audits and inspections. Required Skills Analytical chemistry HPLCGCMass spectrometry Chromatography data systems (e.g., Empower, Chromeleon) GMP/GLP compliance Method validation and transfer Laboratory information management systems (LIMS) Stability testing Team leadership and people management