Charles River Laboratories Scientist - Discovery - Bioanalytical in Mattawan, Michigan
Scientist - Discovery - Bioanalytical
Req ID #: 88579
Mattawan, MI, US, 49071
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.
We are seeking an Scientist for our Bioanalytical Team located in Mattawan, MI.
TheScientistin Drug Metabolism Pharmacokinetics (DMPK) is responsible for developing and/or validating methods and/or procedures, to either quantify/synthesize chemical entities, or prepare formulated test articles or supporting compounds, or conduct studies of chemical compounds invitro or in vivo, according to applicable Standard Operating Procedures (SOPs), study protocols and/or GxP regulations. Individuals in this role demonstrate expertise in their field, lead others through scientific mentorship and/or publications, complete assigned projects on time, and communicate effectively. A Scientist is expected to work independently, participate in process improvement initiatives, may supervise others, and may function as a Principal Investigator, Contributing Scientist, and/ or Study Director.
The following are the minimum requirements related to the Scientist position.
HS/GED/Associate degree and 15 or more years of relevant experience; or
Bachelor’s/Master’s degree in a relevant field and 7-10 years of relevant experience; or
Doctoral degree in a relevant field and 2-5 years of relevant experience.
Experience in large molecule LC-MS/MS bioanalysis method development workflows (protein, peptide, oligonucleotides) is strongly preferred.
Use of Sciex triple-quadrupole LC-MS/MS systems is preferred.
Previous experience in a regulated GxP laboratory is preferred.
Proficient using laboratory software applications (i.e., LIMS and data acquisition software).
Working knowledge of GxPs and 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 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.
About Charles RiverCharles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 13,000 employees within 80 facilities in 23 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 80% of the drugs approved by the FDA in 2017.
For more information, please visitwww.criver.com.
Equal Employment OpportunityCharles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet
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