Formulation Specialist

at  Charles River Laboratories

Req ID #: 223933
Montreal, QC, CA
Full time
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 Specialist for our Pharmacy team located at the Senneville site, you will prepare documentation and coordinate all activities related to assigned studies.

In this role, responsibilities may include:

• Prepare the necessary study documents by ensuring that study plans, Standard Operating Procedures (SOP) and budget are respected.
• Coordinate the activities of the assigned studies in accordance with the study plan and study schedule.
• Act as a resource person to resolve technical problems (troubleshooting).
• Participate in technical work in the laboratory when their help is required.
• Participate in the writing and/or modifying of SOP’s when their help is required.
• When their help is required, ensure that all pertinent data is reviewed based on the timelines and in compliance with Good Laboratory Practices (GLP), analytical procedures and study plans.
• When their help is required, be responsible for the reception and shipping of packages (such as samples, test material and other products), to register them, keep their inventory up to date and make sure of their availability during studies.

• Prepare the necessary study documents by ensuring that study plans, Standard Operating Procedures (SOP) and budget are respected.
• Coordinate the activities of the assigned studies in accordance with the study plan and study schedule.
• Act as a resource person to resolve technical problems (troubleshooting).
• Participate in technical work in the laboratory when their help is required.
• Participate in the writing and/or modifying of SOP’s when their help is required.
• When their help is required, ensure that all pertinent data is reviewed based on the timelines and in compliance with Good Laboratory Practices (GLP), analytical procedures and study plans.
• When their help is required, be responsible for the reception and shipping of packages (such as samples, test material and other products), to register them, keep their inventory up to date and make sure of their availability during studies