This is a 9 month contract
• User Access Management/Support.
• Day-to-day user support for assigned systems and workflows.
• Service Now & SailPoint experience a plus.
• Review and approve user access requests.
• Training assignment/verification.
• SumTotal experience a plus.
• Perform annual system user access reviews.
• Selection Value Maintenance (Master List Data).
• Analyse proposed selection field changes for impact in collaboration with IT.
• Review, approve and track system selection value changes.
• Support QMS records (Deviation, CAPA, Effectiveness Check, Change Control) within Track Wise or Veeva Vault QMS as requested.
• Monitoring and completion of record as requested.
• Minimum of bachelor’s degree in Life Sciences (or similar technical bachelor’s degree).
• 1-3 years of directly related experience in pharmaceutical or biotechnology industry – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
• The successful candidate will also have demonstrated the ability to deliver what is needed on-time, holding self and team members accountable for commitments, decisions, actions, and behaviours.
• The successful candidate will also have excellent oral and written communication skills, with the ability to effectively articulate understanding of process science, to drive decision making, impact assessments, design of studies, etc.
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