Sample Management - Technical Specialist Shipping (CITES permit)

Charles River; Senneville; On-site; CAD 50,000 - 70,000; Full time

Job summary

A leading company is seeking a Technician specialist I for their Sample Management department in Montreal. This role involves preparation of CITES permits, overseeing material shipments, and ensuring compliance with regulatory requirements. Candidates should have a college diploma and experience in a similar role, along with bilingualism in French and English.

Benefits

Free shuttle service

Competitive benefits

Free gym on site

Annual bonus based on performance

3 weeks vacation & 5 personal days

Qualifications

• Minimum 2 years experience as Technician II in Sample Management.
• Ability to perform activities autonomously under pressure.
• Flexible and adaptable to change.

Responsibilities

• Preparation of CITES permit and perform standard technical activities.
• Assist study specialist and oversee shipment of materials.
• Ensure compliance with GLP and SOP requirements.

Skills

Organized

Autonomous

Bilingual (French/English)

Education

College diploma

Job description

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Sample Management - Technical Specialist Shipping (CITES permit)

Location:

Montreal (Senneville), Quebec, CA, H9X 3R3

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

As a Technician specialist I for our Sample Management department at the Senneville location, you will be responsible of CITES permits. You will also perform basic and specialized procedures with little or no supervision.

In this role, primary responsibilities include:

• Preparation of CITES permit
• Perform standard technical activities linked to his area of expertise.
• Assist study specialist in their functions and can oversee shipment of material.
• Involve in the process improvements.
• Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the GLP, SOP and health and safety.

We are looking for the following minimum qualifications for this role:

• College diploma and/or a minimum of 2 years of experience as Technician II in Sample Management. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Evidence of flexibility and ability to work independently.
• Perform the activities autonomously in a timely fashion by adhering to preset schedules.
• Organized and able to adapt to change.
• Comfortable working on a computer.
• Ability to work under pressure and time constraint.
• Master the technical responsibilities in their area of expertise.
• Bilingualism is required (French/English).

Role Specific Information:

• Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station
• Pay: As per salary scale.
• Annual bonus based on performance.
• Schedule: Monday to Friday (7 AM-3:15PM) depending on the needs you may have to work in overtime.
  Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

• Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
• Free gym on site.
• Employee and family assistance program.
• Excellent welcome program for new employees as well as in-house advancement and career development opportunities.
• Access to a doctor and various health professionals (telemedicine).
• 3 weeks’ Vacation & 5 Personal day policy.
• Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

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.

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 [e-mail]. 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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