Watson Lims Optimization Manager

6 days ago


Laval, Canada Altasciences Full time

**Your New Company** At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. Â No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. **About The Role** The Watson LIMS Optimization Manager is the Subject Matter Expert and is responsible for overseeing global activities required to support Watson LIMS within Altasciences Laboratory Sciences. **What You'll Do Here** - Licenses management; procurement and account access - Justifies capital and/or operational expenses - Collaborate with departments managers to identify training needs and implement training program - Provides training to employees - Identify trainers and coordinates training schedule - Continuous improvements of training program - Works with IT development team to establish priorities for the development and validation of custom reports - Provides technical support to technicians, analysts and scientists. - Investigate and troubleshoot errors - Works closely with IT for reporting bugs to vendor and implement fixes - Elaborates Watson upgrade plan and ensures proper deployment - Identifies technical needs to expand usage of Watson LIMS within Altasciences - Works with IT validation team to approve validation plan and change controls for instrument integration, modules and ad hoc tools - Participate in customer advisory board - Participate in process improvements initiatives. - Review and updates SOP - Harmonizes SOP and training across sites - To conduct all work in compliance with SOPs, GLPs, GCPs and observe all company guidelines and policies. - To perform any other tasks as required. '‹ **What You'll Need to Succeed** - B.Sc. or higher in Life Sciences or Bioinformatics - Relevant experience in Sample Management, Ligand Binding Assays and/or Mass Spectrometry - Experience working in a CRO - Knowledge of Watson LIMS is mandatory - Knowledge of FDA-GLP, GCP and TPD regulation is an asset. - Must have a valid passport and available to travel within North America when necessary (



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