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Charles River Laboratories: Supervisor Necropsy 1

Charles River Laboratories

This is a Full-time position in Ashland, OH posted September 29, 2021.

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies.

When you join our family, you will have a significant impact on the health and well-being of people across the globe.

Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform.

In return, we’ll help you build a career that you can feel passionate about.Job SummaryWe are seeking an experienced Supervisor Necropsy for our Safety Assessment site located in Ashland, OH.Oversee the necropsy laboratory and associated technical personnel.

Act as the primary point of contact in matters pertaining to area of responsibility within the laboratory.

Responsible for adherence to established guidelines of this area.The following are minimum requirements related to the Supervisor Necropsy position:Oversee daily operational activities and supervision of staff.

Ensure optimum group performance.Manage inventory and supply ordering.Oversee development of special procedures (technical specialties, difficult protocol-specific processes, etc.)Provide guidance and training to less experienced staff.Supervise departmental procedures for sample receipt, handling, tracking, transfer, and shipping.Assist technical staff as needed in all laboratory tasks to ensure timely completion of study related activities.About Safety AssessmentCharles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.

From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.

Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.