The Specialist Stability, Logistics & Enrollment coordinates the stability sample management activities The activities include receipt of new stability samples for enrollment, study creation, label generation, staging into stability chambers, timepoint pull and inventory management.
Your main responsibilities
Responsible for the handling of commercial stability sample management for internal products:
o reception of samples,
o LIMS setup
o stagging in chamber, which included labeling
o pulling at define time point
o transfer samples to QC labs,
o destruction of sample
Author stability initiation documents or others related documents
Perform stability data reporting and data trending for internal and external stability studies, as needed
Organize the stability chambers cleaning and perform monthly check/maintenance.
Capability of solving problems with a minimum guidance
Ensure training requirement are met
Support global stability team on adhoc requests.
Your Qualifications
Bachelor in Chemistry, Biology, Microbiology or relevant discipline
1 - 3 years of relevant work experience in a Pharmaceutical environment
Good understanding of pharmaceutical regulatory requirements and guidelines and their impact to commercial laboratory operations
Good knowledge in stability study guidelines and cGMP
Knowledge of LIMS software
Good written and verbal communication skills
Problem solving ability
Able to set priorities to meet timelines and to adapt quickly to changes in schedule in order to accommodate priority requests.
Ability to work independently and contribute to a team based environment.
Intermediate knowledge of Microsoft Word, Outlook, and Excel
Fluent knowledge in English and French
Carmen Acz\\xc3\\xa9l is looking forward to receiving your application:
reference number: 2294
by mail to or through our website . Full discretion is guaranteed and we will gladly answer any additional questions.\\n \\n \\n \\n \\n \\n