AbbVie
Senior Manager, Quality Control Laboratory
AbbVie - Kansas City, Missouri, United States, 64111
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Overview
Senior Manager Of Quality Control Laboratories
We are currently looking for a Senior Manager of Quality Control Laboratories to join our team in Westport on a 12-month fixed-term contract. The Senior Manager of Quality Control is responsible for strategy, planning, and management of laboratory operations, ensuring compliance with FDA, HPRA, and EPA safety standards and budgetary constraints. This role supports the QA site head in achieving operational goals. Responsibilities: Manage and motivate employees, ensuring capacity aligns with business needs. Develop and deliver business plans, manage departmental budget, and handle new product implementation. Represent the company in client and regulatory meetings, ensuring GMP compliance. Organize cross-functional activities to improve lab efficiencies. Coordinate meetings and manage documentation and compliance tools. Qualifications: Proven track record in people and operations management within Pharma/Medical Devices/Food industry. Qualification in Pharmaceutical Science. Excellent conflict resolution, planning, and communication skills. Ability to manage in regulated environments and adapt to changes. Strong commitment to AbbVie's values and business ethics. 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.
We are currently looking for a Senior Manager of Quality Control Laboratories to join our team in Westport on a 12-month fixed-term contract. The Senior Manager of Quality Control is responsible for strategy, planning, and management of laboratory operations, ensuring compliance with FDA, HPRA, and EPA safety standards and budgetary constraints. This role supports the QA site head in achieving operational goals. Responsibilities: Manage and motivate employees, ensuring capacity aligns with business needs. Develop and deliver business plans, manage departmental budget, and handle new product implementation. Represent the company in client and regulatory meetings, ensuring GMP compliance. Organize cross-functional activities to improve lab efficiencies. Coordinate meetings and manage documentation and compliance tools. Qualifications: Proven track record in people and operations management within Pharma/Medical Devices/Food industry. Qualification in Pharmaceutical Science. Excellent conflict resolution, planning, and communication skills. Ability to manage in regulated environments and adapt to changes. Strong commitment to AbbVie's values and business ethics. 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.