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Associate Scientist-Discovery Bioanalytical

Charles River Laboratories
Mattawan, MI
Closing date
Jan 18, 2022

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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 Summary
We are seeking an Associate Scientist for Discovery Bioanalytical Team located in Mattawan, MI.

The Associate Scientist in Discovery Bioanalytical is responsible for developing and qualifying LC-MS/MS methods; analyzing sample according to applicable Standard Operating Procedures (SOPs), study protocols and regulations. Individuals in this role demonstrate expertise in their field, lead others through scientific mentorship, complete assigned projects on time, and communicate effectively. An Associate Scientist is expected to work independently, participate in process improvement initiatives, supervise junior technical staffs.
Job Qualifications
The following are the minimum requirements related to the Associate Scientist position.
  • PhD in a relevant field and 0-2 years of relevant experience; or
  • Bachelor's/Master's degree in a relevant field and 3-5 years of relevant experience
  • Experience in LC-MS/MS bioanalysis method development workflows
  • Proficient using laboratory software applications (i.e., LIMS and data acquisition software).
  • Working knowledge of industry guidance documents.
  • Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts and/or extra shifts, sometimes on short notice.
  • Familiarity with Microsoft Office Suite.
  • Ability to work under specific time constraints.

About Safety Assessment
Charles 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 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
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