We're committed to bringing medicines to the world at a faster pace without compromising on excellence and integrity. Adhering to both local and global regulations is crucial, and the constantly evolving regulatory landscape demands forward-thinking and meticulous attention to detail. Your dedication and expertise are vital in expanding and accelerating patient access to Pfizer's medicines and vaccines. Your role will be essential in ensuring that our regulatory submissions are prepared, published, tracked, and quality-controlled to meet the highest standards, ultimately supporting patients globally.
What You Will Achieve
In this role, you will:
- Assist in the preparation, publication, tracking, and quality control of regulatory submissions, ensuring compliance with document management standards.-
- Make decisions within limited options to resolve basic problems under the supervisor's direction, working in a structured environment using established procedures.- Ensure work is regularly reviewed for technical judgment, completeness, and accuracy,
exercising judgment with reliance on the supervisor.- Execute designated operational tasks using standards and tools, conforming to regulatory submission milestones and obligations.- Help interpret regulatory guidelines to produce business requirements and ensure their implementation at the local level, promoting quality as a best practice.- Support regulatory activities associated with new food supplements in development and 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 general load sharing.- Communicate with internal team members about execution and strategy as needed, actively pursuing training in technical and personal skills relevant to the role.
Here Is What You Need (Minimum Requirements)- Applicant must have a bac
📌 Hub Dossier Associate I (Suba)
🏢 Pfizer
📍 Suba
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