Trainee Executive
Pfizer Canada Inc.
Chennai, India
2d ago

ROLE SUMMARY

  • Delivery of electronic and paper regulatory transactions in support of New Product Launches, Legalizations, and License maintenance (eg, COPP , GMP , FSC certifications etc)
  • Continuous Improvement of selected processes relating to human health submissions and selected drug and non-drug specific projects and related activities (e.g. legalizations)
  • Subject matter expert of Pfizer’s positions in support of proposed changes
  • ROLE RESPONSIBILITIES

  • Delivery of Product License Support Portfolio
  • Identify opportunities and implement solutions through interaction with other team members, and key contributors across sites, ensuring ability to maintain compliance with assigned processes and continuously improve on those processes
  • Knowledge share and educate personnel as appropriate on agency requirements and guidelines.
  • Lead or participation on global / local teams to complete assignments and tasks within a specific task force / project.
  • Process development and change management in the context of PLS submissions
  • Liaison with internal stakeholders for issues regarding standards and processes, and drives resolution
  • Utilization support of electronic technologies for submissions and tracking of documentation
  • Matrix management of cross-functional teams as appropriate
  • Development and maintenance of documented procedures and guidelines as necessary
  • Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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