LIMS Optimization Expert
1 week ago
We are seeking a highly skilled LIMS Optimization Expert to join our team at Planet Technology.
About the RoleThe successful candidate will be responsible for overseeing global activities in support of Watson LIMS, with a focus on optimizing and improving system performance.
Responsibilities- Serving as Subject Matter Expert (SME) in the oversight of global activities required in support of Watson LIMS
- Collaborating with departmental management to identify user training needs and implementing these into the training program
- Identifying key user training experts and coordinating training schedule
- Ensuring continuous improvements to the training program
- Working with IT development teams to establish and prioritize validation and custom reports required within an FDA, GLP, GCP, and TPD regulated environment
- Providing technical support to technicians, analysts, and scientists
- Investigating and troubleshooting errors for users with expertise in Sample Management, Ligand Binding Assays, and/or Mass Spectrometry
- Working closely with IT in the reporting of bugs to vendor, while liaising to implement fixes
- Assisting with Watson upgrade plans and ensuring proper deployment
- Identification of Watson LIMS technical needs based on organizational business needs
- Working with IT validation teams in the approval of validation plans and change controls for instrument integrations, modules, and ad-hoc tools
- Participating on the customer advisory board for process improvement initiatives
- Reviewing and updating SOPs to ensure harmonization across training sites
- Conducting all daily tasks in compliance with SOPs, GLPs, GCPs, and all other organizational guidelines and policies
- Managing licenses and procurement across all accounts to ensure proper security access and onboarding/offboarding license tracking and assistance
- Ensuring technical initiatives are justified based on capital and operational expenses
- You have 2+ years' experience in Watson LIMS, having worked within an FDA, GLP, GCP, and TPD regulated environment
- You have exposure to Sample Management, Ligand Binding Assays, and/or Mass Spectrometry
- You possess strong communication skills in both English and French
- You have worked within a Contract Research Organization (CRO) prior
- Estimated Salary: $95,000 - $115,000 per annum, dependent on individual expertise and seniority
- Medical Group Insurance
- Group RRSP with a 100% match of 3% of annual salary contributed each pay period
- A Telemedicine program
- 3 weeks' vacation
- 6 days PTO
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