Associate Scientist- Project Scientist

Associate Scientist- Project Scientist Req ID #:  213647 Location: 

Mattawan, MI, US, 49071 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 experienced Associate Scientist- Project Scientist for our Immunochemistry team located in Mattawan, MI.

The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay, to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic assays to measure drug and Immunogenicity assay to measure anti-drug antibodies and neutralizing antibodies. Other assay types also performed are branched DNA and cell-based assays.

Essential Functions (The fundamental Competencies/Skills& Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed: 

Effectively manage a small portfolio of sample analysis projects while ensuring timelines are met in a single operational area with oversight

Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area

Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with oversight

Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations

Assist in problem solving for technical and/or regulatory issues with oversight

Responsible for writing and preparing study plans/protocols/amendments with oversight

Participate in Sponsor visits/tours with oversight

Develop expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational areas with oversight

Perform data analysis using appropriate software with oversight

Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas

Demonstrate effective communication skills through informal discussions with peers, supervisor, and team Job Code - Title:

Function as a liaison, maintaining timely and frequent communication between CRL and Sponsor/Client/SD with oversight

Ensure scientific integrity of studies with oversight

Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with oversight

Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data

Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)

Write, review and approve deviations with oversight Job Qualifications

The following are minimum requirements related to the Associate Scientist- Project Scientist position.

Bachelor's degree (BA/BS) with 3-5 years of relevant working experience. Master's degree (MS) with no previous work experience

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above

Ability to communicate verbally and in writing at all levels inside and outside the organization

Basic familiarity with Microsoft Office Suite

Computer skills, commensurate with Essential Functions, including the ability to learn a validated system

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

Ability to work under specific time constraints

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 www.criver.com.

Nearest Major Market: Kalamazoo

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