Supervisor Histopathology

Supervisor Histopathology Req ID #:  119611 Location: 

Laval, Quebec, CA, H7V 4B3 For 70 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 a Supervisor Histopathology to join our team located in Laval. 

Coordinate and supervise the performance of technical procedures in the terminal investigation of animals assigned to a study (investigation or development). Manage assigned technicians in a way that maximizes team performance.

The following are the minimum qualifications:

•    Supervise the performance of necropsy and histology technical procedures in the terminal investigation of animals assigned to a study (investigation or development);

•    Ensure that work performed is in accordance with the requirements of the study plan and in full compliance with Good Laboratory Practices (GLP), where these conditions apply;

•    Ensure application of all Standard Operating Procedures (SOPs);

•    Ensure completion and integrity of data collection;

•    Ensure all necessary materials for necropsy and histology projects are in working order, when required;

•    Prepare and maintain the pathologists schedule up to date;

•    Manage each necropsy or histology projects from preparation stage to revision, including responding to QA reports and the revision of master and study plan;

•    Monitor all necropsy and histology projects and give necessary feedback to the Study Director and Pathologist;

•    Discuss job requirements with the Director of Technical Services, team leaders and with necropsy and histology team members;

•    Plan the work of team members to maximize efficiency and productivity;

•    Ensure samples are in good order and sent to the personnel responsible for courier coordination;

•    Prepare chain of custody and shipment documentation;

•    Be actively involved in the recruiting process;

•    Monitor and evaluate performance of Necropsy and Histology team leaders;

•    Monitor and evaluate performance of Necropsy and Histology technicians in collaboration with the team leader;

•    Train the team leader to optimize team performance;

•    Offer development opportunities;

•    Write and review SOPs;

•    Substitute and/or assist department colleagues;

•    Provide necessary assistance to Study Director, Pathologist and Sponsor;

•    Maximize the utilization of all resources.

•    Manage time effectively;

•    Monitor the calibration of Necropsy equipment.

  Job Qualifications  

The following are the minimum qualifications related to the Supervisor Histopathology position:

•    Collegial Diploma in Chemistry, Biology or equivalent;

•    A minimum of 5 – 7 years of relevant experience, including personnel and project management;

•    Excellent knowledge of related legislation, principles, practices and procedures;

•    Excellent knowledge and application of GLP;

•    Reading of English is required. Bilingualism is preferable;

•    Strong organizational, interpersonal and communication skills;

•    Strong problem solving and analytical skills;

•    Ability to work under time constraints and adapt to change;

•    Flexibility to work on changing work schedules;

•    Ability to work in a team environment;

•    Detail oriented and meticulous;

•    Ability to efficiently manage people, time and resources;

•    Demonstrated leadership ability;

•    Working knowledge of related computer applications.

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 17,000 employees within 90 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. And in 2019, revenue increased to $2.62 billion.

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 ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

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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