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Associate Toxicologist Jobs in Michigan (NOW HIRING)

Warehouse Associate

Mount Clemens, MI · On-site

$15 - $17.75/hr

Our Opportunity We are currently seeking a Warehouse Associate to join our team of professionals ... toxic chemicals * Other duties as needed What We Are Looking For Related experience in a similar ...

Warehouse Associate

Mount Clemens, MI · On-site

$15 - $17.75/hr

Our Opportunity We are currently seeking a Warehouse Associate to join our team of professionals ... toxic chemicals * Other duties as needed What We Are Looking For Related experience in a similar ...

Warehouse Associate

Mount Clemens, MI

$15 - $17.75/hr

Our Opportunity We are currently seeking a Warehouse Associate to join our team of professionals ... toxic chemicals * Other duties as needed What We Are Looking For Related experience in a similar ...

Parts Associate

Taylor, MI · On-site

$14.75 - $20/hr

Parts Associate Department : Parts Supervisor: Parts Manager Summary Description Provide courteous ... Potential exposure to battery acid, gasoline, chemical cleaning materials or other toxic materials ...

Parts Associate

Farmington Hills, MI · On-site

$15.75 - $21.25/hr

Parts Associate Department : Parts Supervisor: Parts Manager Summary Description Provide courteous ... Potential exposure to battery acid, gasoline, chemical cleaning materials or other toxic materials ...

Parts Associate

Taylor, MI

$14.75 - $20/hr

Parts Associate Department : Parts Supervisor: Parts Manager Summary Description Provide courteous ... Potential exposure to battery acid, gasoline, chemical cleaning materials or other toxic materials ...

Parts Associate

Farmington Hills, MI · On-site

$15.75 - $21.25/hr

Parts Associate Department : Parts Supervisor: Parts Manager Summary Description Provide courteous ... Potential exposure to battery acid, gasoline, chemical cleaning materials or other toxic materials ...

Parts Associate

Taylor, MI · On-site

$14.75 - $20/hr

Parts Associate Department : Parts Supervisor: Parts Manager Summary Description Provide courteous ... Potential exposure to battery acid, gasoline, chemical cleaning materials or other toxic materials ...

Office Associate

Flint, MI · On-site

$17 - $22/hr

The Office Associate effectively operates the front desk position for the distributorship ... and toxic or caustic chemicals. * Specific vision abilities include close vision ...

Vehicle Sales Associate

Dimondale, MI · On-site

$14.75 - $20.25/hr

Sales & Lead Associate Department..... Sales Department Supervisor..... Sales Manager Summary ... other toxic materials commonly found in a motor vehicle service department. · Occasionally ...

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Showing results 1-20

Associate Toxicologist information

See Michigan salary details

$35.7K

$100.6K

$186.5K

How much do associate toxicologist jobs pay per year?

As of Sep 2, 2026, the average yearly pay for associate toxicologist in Michigan is $100,555.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,200.00 and $118,100.00 per year, depending on experience, location, and employer.

What does an associate toxicologist do?

An Associate Toxicologist assists in evaluating the safety and potential health risks of chemicals, drugs, or environmental substances. They conduct laboratory experiments, analyze toxicological data, and prepare reports to support regulatory compliance and risk assessments. They may also contribute to research studies and collaborate with other scientists to ensure product safety. This role is common in industries such as pharmaceuticals, environmental health, and consumer product safety.

What are the key skills and qualifications needed to thrive as an associate toxicologist?

To thrive as an Associate Toxicologist, you need a background in toxicology, chemistry, or a related biological science, often supported by a relevant bachelor's or master's degree. Familiarity with laboratory information management systems (LIMS), analytical instruments such as GC-MS/LC-MS, and adherence to regulatory guidelines like GLP or EPA standards are typically required. Attention to detail, critical thinking, and effective communication are essential soft skills, as is the ability to work collaboratively in cross-functional scientific teams. These capabilities ensure reliable testing results, regulatory compliance, and contribute to the overall success of research and safety evaluations.

Can you work remotely in associate toxicologist?

Whether an associate toxicologist can work remotely depends on the employer and specific job responsibilities. Some positions may allow remote work, especially those focused on data analysis, report writing, or research, while others requiring laboratory or field work typically require on-site presence. It is important to review job postings and discuss remote options during the application process.

Is there a demand for associate toxicologists?

The demand for associate toxicologists is steady, especially in industries such as pharmaceuticals, environmental health, and regulatory agencies. Employment opportunities are often driven by ongoing research, safety testing, and compliance requirements, with roles requiring knowledge of toxicology principles and relevant certifications.

What are some associate toxicologist entry level jobs?

Entry-level associate toxicologist positions typically involve supporting research, data collection, and analysis related to chemical safety and toxicology assessments. These roles often require a bachelor's degree in toxicology, chemistry, or a related field, and may involve working in laboratory or regulatory environments under supervision.

What are the most commonly searched types of Toxicologist jobs in Michigan?

The most popular types of Toxicologist jobs in Michigan are:

What are popular job titles related to Associate Toxicologist jobs in Michigan?

For Associate Toxicologist jobs in Michigan, the most frequently searched job titles are:

Infographic showing various Associate Toxicologist job openings in Michigan as of August 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $100,555 per year, or $48.3 per hour.

Study Director I - General Toxicology

Charles River Laboratories, Inc.

Mattawan, MI

$85K - $88K/yr

Full-time

Medical, Retirement, PTO

Posted 5 days ago


Charles River Laboratories rating

8.4

Company rating: 8.4 out of 10

Based on 94 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical


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.

Job Overview

We are seeking an experienced Research Scientist I for our General Toxicology Study Director Team in Mattawan MI.

A Research Scientist I - Safety Assessment serving as a study director (SD) is responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies assigned by test facility management (TFM) within safety assessment; overseeing protocols/study plans; coordinating with technical teams for execution of studies, including establishing study schedules, verifying that standard operating procedures (SOPs) are available and adhered to, overseeing data recording and reporting, and verifying that regulatory requirements/expectations are met. The individual in this role interprets preclinical toxicity studies, evaluates and prepares reports from the data collected during these studies, communicates with sponsor representatives, and initiates contact with potential clients. May be involved with development of new technologies/procedures.

The pay range for this position is $85,000 to $88,000/yr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Description
  • Function as an independent SD, working on studies/programs of basic to moderate complexity. See detailed role and responsibilities of Study Director below:
  • Design, write, review and edit study plans/protocols, amendments and study schedules that define and schedule all study activities.
  • Oversee and coordinate study procedures.
  • Verify that projects are performed according to SOPs and good laboratory practices (GLP) regulations.
  • Write, review and edit draft or final reports that document all study related procedures and results.
  • Communicate with sponsors on study related business.
  • Oversee and coordinate study conduct (protocol development, technical guidance, and reporting).
  • Assist in study planning, scheduling, and execution under the supervision of Sr. Scientist(s)/Scientific Manager.
  • Host client visits and telephone/video conferences.
  • Assists with mentoring less experienced staff and may assist with training of scientific/senior scientific associates as needed.
  • Provides advice to clients and technical teams.
  • May assist with proposal development.
  • Develop an area of expertise.
  • Other duties as assigned.
Minimum Requirements
  • Bachelor’s degree or equivalent in Toxicology or a related discipline; Master’s/PhD/PharmD/DVM/MD degree or equivalent preferred; with 2 or more years of related industry experience.
  • Data interpretation of in-vivo toxicology studies preferred.
  • Overseen or conducted in-vivo toxicology studies preferred.
  • Experience in understanding and implementation of US FDA guidance documents in relation to preclinical testing preferred.
  • Success in this role requires familiarity with: study/project costs and impact of changes, local regulations and GLPs as they relate to primary area of focus, study process from proposal to report, quality assurance (QA)/quality control (QC) processes, IACUC process, the SD role in animal welfare, effective communication with veterinary staff and internal/external clients in a manner that generates confidence and builds trust, and communication with technical supervisor and Scientific Manager on issues of staffing and equipment.
  • Strong communications skills, 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.
  • Must be authorized to work in the United States without a sponsor visa, now or in the future.

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.


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 over 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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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.


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About Charles River

Sourced by ZipRecruiter

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.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947