Watson Lims Optimization Manager

4 weeks 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. 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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