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Charles River Laboratories: Histology Coordinator 1

Charles River Laboratories

This is a Full-time position in Ashland, OH posted September 27, 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 a Histology Coordinator for our Safety Assessment site located Ashland, OH.The following are responsibilities related to the Histology Coordinator:Independently perform advanced histology (slide QC, special stains, thin/thick sections, IHC, and serial/step sectioning).Prepare responses to audits, deviations, and other documentation from internal and external reviews of data.Perform method development experiments trouble shoot technical challenges, and/or offer solutions to technical challenges.Prepare study specific procedure documentation.The following are minimum qualifications related to the Histology Coordinator position:Education: High school diploma or General Education Degree (G.E.D.) required.

Bachelor’s degree or equivalent in a biological science preferred.Experience: 3 years of pathology laboratory experience.An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.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.