Sample Management Technician 1 1 1
2 weeks ago
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 for our Sample Management department at the Senneville location, you will perform sample management activities and follow directives from the study plan, phase plan and the SOP.
In this role, key responsibilities may include:
- Perform reception, verification, storage, and sample inventories using the Watson LIMS® system. Also perform data review.
- Generate study design in Watson LIMS® based on the study plan or phase plan.
- Perform the follow-up and the preparation of the sample shipment to other departments and/or locations.
- Prepare kits for clinical studies based on the laboratory manual.
- Supervise some technical functions and participate in training performed by less experienced employees.
- Identify problems or potential problems and establishing and implementing the appropriate solutions.
**Job Qualifications**
If you possess the following qualities, we will train you in the rest:
- Highschool Diploma
- Basic computer knowledge
- Ability to read and communicate in English
- Ability to quickly adapt to change
**Role Specific Information**:
- Location: Senneville
- Pay: 19.50$
- Schedule: Monday to Friday 08:00 to 16:15
**Why Charles River?**
- Competitive benefits we pay 90% of premiums (health and dental coverage).
- Access to a savings and retirement program including an employer contribution.
- 3 weeks’ Vacation & 5 Personal / Sick Days
- Free telemedicine app for you and your family.
**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.
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