Associate Scientist I

• Maintain schedules for periodic reviews of test method assays in collaboration with the management and analytical SMEs. Monitor tasks progress and identify potential planning risks
• Manage change control activities related to test method assay periodic reviews and updates in accordance with project needs and agreed timelines
• Contribute to R&D analytical activities by reviewing experiments within her/his area of technical expertise
• Support analytical projects through effective collaboration in documentation management
• Contribute to the continuous improvement of quality processes within R&D analytical laboratories

• Knowledge of small molecules analytical projects
• Organizational skills with demonstrated attention to detail
• Ability to apply a logical and methodical approach to analytical and quality processes and to formulate sound recommendations
• Good understanding of GMP standards in a laboratory environment
• Ability to work on multiple tasks simultaneously while meeting deadlines
• Strong interpersonal skills with the ability to collaborate effectively within cross-functional teams
• Quality-oriented mindset
• Master in Science degree (e.g. Analytical Chemistry, Organic chemistry, Biochemistry, Bio-engineering, Pharmaceutical Science)
• Minimum of 2-6 years of experience in pharmaceutical industry (R&D, manufacturing…)
• Demonstrated expertise in reviewing analytical chemistry data (e.g. experiments, reports)
• Good knowledge of GMP requirements
• Fluent in spoken and written English is mandatory
• Knowledge of Trackwise is an asset

Knowledge of Trackwise is an asset

• Support for Parents
• Continuing Education/ Professional Development
• Employee Heath & Well-Being Benefits
• Paid Time Off
• 2 Days a Year to Volunteer