Technician - Formulations

Charles River Laboratories, Research Models and Services, Germany GmbH; Sherbrooke; On-site; CAD 30,000 - 60,000; Full time

Job summary

Join Charles River as a Technician in Sherbrooke, where you will prepare dosing formulations and ensure timely delivery for administration. This permanent position offers competitive benefits, training opportunities, and a collaborative work environment, impacting health and well-being worldwide.

Benefits

Competitive health & dental coverage

Savings and retirement program

Free gym on site

Access to health professionals

Excellent welcome program for new employees

Qualifications

• Self-starter with collaborative and positive attitude.
• Able to work physically (lift, walk, stand).
• Qualifications in Science or Biopharmaceutical Production.

Responsibilities

• Prepare formulations for dosing in various methods following GLP.
• Execute technical activities as per procedures and study plans.
• Ensure availability of components for laboratory activities.

Skills

Collaborative attitude

Understanding of written English

Physical ability to lift up to 10 kg

Education

DEC in Science

AEC in Biopharmaceutical Production

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

Technician – Formulations

As a Technician for our Formulations team in Sherbrooke, you will be responsible to prepares all the dosing substances in different concentrations and ensures the timely delivery of these dosing for administration.

In this role, key responsibilities include :

• In accordance with study plans, you will prepare the formulations for dosing either in solution, suspension capsule, or powder mixture. You will also handle samples under a Fume Hood using an aseptic method.
• Execute the technical activities described in the procedures and study plans while respecting the Good Laboratory Practices (GLP).
• Check the availability and prepare all required components related to its laboratory activities (literature, samples, solutions, material, equipment, etc.).

If you possess the following qualifications , we will train you in the rest :

• A self-starter with a collaborative and positive attitude
• Being able to work physically (lift up to 10 kg, walk, stand, stoop, etc.);
• Understanding of written English
• DEC in Science, Pharmaceutical Process Control, or Biopharmaceutical Production Technology; or an AEC in Biopharmaceutical Production. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Role Specific Information :

• Transportation : Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
• Pay : Starting at 23.00$ / hrs. Opportunity to start at higher level and higher salary with specific research experience.
• Schedule : Full time, permanent position (37.5 hours / week), depending on the needs, you may have to do overtime and work on weekend (bonus of $2.75 / hour).

Why Charles River?

• Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
• Access to a savings and retirement program that includes an employer contribution.
• 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).
• Free gym on site.

If you want to contribute to the wellbeing of our communities across the country and around the world, join our team. 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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 [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.