Job Overview

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Employment Type

Full-time
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Compensation

Hourly
Exact $21.70
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Benefits

bonus/incentives
401k
Paid Time Off
stock purchase program
health coverage
wellness programs
Work life balance flexibility

Job Description

Charles River Laboratories is a renowned early-stage contract research organization (CRO) that has been supporting the pharmaceutical and biotechnology industries for over 75 years. With a strong foundation in laboratory animal medicine and science, Charles River has expanded its expertise to deliver a diverse portfolio of discovery and safety assessment services. This includes both Good Laboratory Practice (GLP) and non-GLP studies, assisting clients from target identification through to preclinical development and clinical laboratory testing needs. The company operates across more than 110 facilities in over 20 countries worldwide, employing over 20,000 professionals dedicated to advancing drug discovery and development. Their global client base includes major pharmaceutical companies, biotech firms, government agencies, hospitals, and academic institutions.

Charles River is deeply committed to improving human health by providing exceptional services that accelerate the drug development process. Their mission is guided by scientific excellence and a strong sense of purpose, contributing to the approval of approximately 80% of the drugs sanctioned by the U.S. Food and Drug Administration in the last five years. This long-standing expertise and commitment have positioned Charles River as a trusted partner in the life sciences industry.

This role involves preparation of article/substance dosage solutions or suspensions according to specific client specifications for use in toxicology studies. The position is essential within the Safety Assessment division, where employees contribute directly to preclinical drug development through the preparation and management of test articles and substances. The job requires adherence to standardized procedures and meticulous documentation to ensure consistency and compliance with regulatory standards. Employees in this role are responsible for the preparation of labels and samples, receiving test articles and reagents, maintaining laboratory cleanliness, sample shipment, and responding to quality assurance audits, among other critical tasks. The position offers a wage of $21.70 per hour, with compensation varying based on experience, education, skills, and certifications.

The ideal candidate will have a Bachelor’s degree or equivalent and 0 to 2 years of relevant experience. Working knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is preferred, as the role demands strong attention to detail, organizational skills, and accurate record-keeping capabilities. Charles River fosters a collaborative and supportive work environment focused on scientific rigor and innovation. This opportunity comes with a comprehensive benefits package aimed at fostering employee well-being and professional growth, including performance bonuses, retirement savings plans, paid time off, health and wellness coverage, and flexible work-life balance options.

Joining Charles River means becoming part of a global team that impacts health and well-being worldwide. Employees take pride in contributing to life-changing therapies and advancing scientific knowledge while growing their careers in a vibrant, mission-driven organization.

Job Requirements

  • Four-year degree required
  • 0 to 2 years of relevant experience
  • Working knowledge of GMP/GLPs preferred
  • Ability to maintain accurate records
  • Strong organizational and attention to detail skills
  • Ability to follow standardized procedures
  • Effective communication skills

Job Qualifications

  • Bachelor's degree or equivalent
  • 0 to 2 years of relevant experience
  • Working knowledge of GMP/GLPs preferred
  • Strong attention to detail
  • Strong organizational skills
  • Accurate record-keeping competencies

Job Duties

  • Perform preparation of test article/substance dosage solution/suspension(s), ensure preparation procedures and calculations are standardized, performed consistently and recorded correctly by technical personnel
  • Prepare labels and samples
  • Receive all incoming test articles/substances and reagents
  • Ensure documentation for the use of all test articles/substances and vehicles/reagents is consistent and correct
  • Responsible for the sampling and shipment of samples
  • Maintain cleanliness and general appearance of the Formulations Laboratory
  • Ensure that test articles/substances from completed studies are returned to the sponsor or reassigned
  • Respond to Quality Assurance audits of preparation procedures and calculations
  • Ensure all chemistry data is submitted to Senior Scientist for weekly review
  • Maintain an up to date inventory of reagents, test articles/substances, vehicles and samples
  • Review chemistry data daily and finalize chemistry data for submission at study completion
  • Prepare accurate packing lists for shipment of test articles/substances and samples to sponsors or analytical laboratories
  • Notify appropriate personnel of shipments
  • Perform other duties as assigned by supervisor

Job Criteria

Experience

No experience required


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