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 Summary

A Technician III is performing basic tasks and procedures within a team, gaining more experience with additional species of focus, and learning more intermediate tasks and procedures of the department training plan. The technician is assigned to work on study to perform tasks which may include serving as lead/primary technician for multiple basic in-life studies simultaneously. Provide leadership and technical guidance in the laboratory. Collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by basic and intermediate methods. Serve as a mentor to less experienced staff. The technician can work more independently, with addition species, and/or perform more complex procedures to support the routine study needs.

• Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
• Perform basic tasks of the department, with little supervision. Tasks may include Parot system use, intradermal dosing on multiple species, intranasal dosing on multiple species, ocular topical and subconjunctival liquids on multiple species. Dermal topical patches on multiple species, blood collection via jugular, cephalic, and tail vein on multiple species. Pipette and microliter use and dosing on multiple species as well as fume hood use. Specific tasks will be based on each area\'s training plan and business needs.
• Collect, document, review, and verify data on forms, or in electronic data capture systems.
• Review documentation of functions performed as part of quality control requirements.
• Use and maintain instrumentation and equipment.
• Perform all other related duties as assigned.

The pay range for this hourly role is $19/hour.

Job Qualifications

• Education: High school diploma or General Education Degree (G.E.D.) with a minimum of 1 year of related experience in a Contract Research environment. Associate (A.A./A.S.) or Bachelor\'s degree (B.A./B.S.) or equivalent in a biological science, animal science, or related discipline with 0 years of related experience.
• Experience: 0-1 year of related experience in a research environment, dependent upon educational background.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.Certification/Licensure: None, unless required by local government. Functional certification, preferred. Others may be required by local government.
• Training plan completed for this role based on department training plan
• Demonstrated ability to consistently and effectively produce high quality results, interpret protocol requirements, troubleshoot quality issues, and record accurate study and departmental data.
• Ability to communicate verbally and in writing at all levels inside and outside the organization.
• Excellent written and verbal communication skills. Knowledge of English.
• Ability to manage multiple tasks and priorities to achieve goals.
• Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
• Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
• Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
• Ability to exercise independent decision-making and self-manage under the direction of a supervisor.
• 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

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 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.

Charles River Laboratories