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Lab Manager- BioPharm- Stability Storage & QC Testing PERM
Ref No.: 17-00248
Location: Middleton, Wisconsin
GMP Laboratories business unit of client is a market leader in providing GMP analytical services to the pharmaceutical, biotechnology, and medical device industries. The client's GMP Laboratories have ~1,100 employees located in Middleton, Wisconsin and Athlone, Ireland. This is an exciting opportunity to join a rapidly growing scientific service business within one of the world's premier drug development companies.

We provide a full complement of state-of-the-art GMP analytical testing resources and expertise to support commercial stability studies, release testing and quality control analyses for active pharmaceutical ingredients and drug products in virtually all dosage forms and delivery systems.

As the Lab Manager (potential for Associate Director for exceptional candidate), Stability Storage & Quality Control (QC) Testing - Biopharmaceutical Services (GMP), your basic purpose will be to ensure efficient and effective management of client resources. You will supervise and assist group leaders and scientists in laboratory operations with tasks such as scheduling, resource management, technical and compliance related issues. In addition, you will plan, direct and implement improvements in systems, processes and procedures to increase efficiency, productivity and quality in the laboratory. You will assist the division director in strategic planning, business development and expansion initiatives by providing mid range (1-3 month) resource utilization predictions for a department.

• B.S. in Chemistry or related science plus 10 or more years experience in a pharmaceutical or biotech laboratory OR
• M.S. in Chemistry or related science plus 8 or more years experience in a pharmaceutical or biotech laboratory OR
• Ph.D. in Chemistry or related science plus at least 6 years experience in a pharmaceutical or biotech laboratory
• 5 years+ management experience in the pharmaceutical, biotech or analytical contract laboratory industries. Management experience should include stability/QC/analytical R&D/ project and program management, direct supervision of technical staff, and direction of laboratory operations and implementation of process and system improvements