Contribute to the completion of project milestones and organize own work to meet project task deadlines.
Execute, through use of standards and tools, designated operational tasks or through the applicable Pfizer country office, conforming to regulatory submission milestones and applicable regulatory obligations.
Help interpret regulatory guidelines to produce business requirements and ensure that those requirements are implemented where appropriate at local level.
Promote quality as a best practice based on knowledge of regulatory requirements, departmental guidelines, and Quality Control (QC) experience.
Support the regulatory activities associated with allocated new food supplements in development.
Compile, verify accuracy, and sort regulatory license information for products identified for withdrawal.
Contribute to effective forecasting and management of project specific resources utilizing flexible resourcing, and global load sharing as normal business practice.
Communicate with internal team members about execution and strategy as needed
Actively pursue training in technical and personal skills relevant to the Certificate Signing Request Coordinator role.
Act as a subject matter expert on global regulatory requirements in the cross functional team.
Qualification & Experience
Bachelor's Degree
Demonstrated experience
Relevant experience in electronic submissions build within the Pharmaceutical Industry
Demonstrated coordination of activities in a highly regulated environment
Demonstrated experience working in a challenging customer service environment