Senior Associate Scientist - Bioanalytical Method Development 1 1 Job at Charles River Laboratories, Inc., Mattawan, MI

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  • Charles River Laboratories, Inc.
  • Mattawan, MI

Job Description

For 75 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.

 

IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.



 

Job Summary

We are seeking an  Senior Associate Scientist for our  Bioanalytical Team site located in  Mattawan, MI .

 

 

The following are responsibilities related to the Senior Associate Scientist :

  An Senior Associate Scientist in Laboratory Sciences is responsible for developing and validating methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. The individual in this role is proficient in the use of instrumentation and laboratory techniques and in the execution of method development and validation procedures. An Senior Associate Scientist is expected to work independently, participate in process improvement initiatives, and may function as a Principal Investigator or Study Director.

Job Qualifications

The following are minimum qualifications related to the Senior Associate Scientist position:

 

  • Bachelors degree (BA/BS) with 5-7 years of relevant working experience. Master's degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with some relevant experience and CRO is preferred. 

  • LCMS Experience Required
  • 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.

The pay range for this position is $70 - 75,000 k/year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. 

 

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

 

About Charles River
Charles 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 20,000 employees within 110 facilities in 20 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 86% of the drugs approved by the FDA in 2021.

 

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

 

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

 

For more information, please visit

Job Tags

Contract work, Work experience placement, Worldwide, Flexible hours, Shift work, Weekend work, Afternoon shift,

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