Regulatory Affairs Specialist
hace 1 mes
Position for Novo Nordisk GBS Mexico
We are seeking a highly skilled Regulatory Affairs Coordinator to join our team in GBS Mexico City. As a key member of our regulatory team, you will play a crucial role in ensuring compliance with regulatory standards and guidelines.
Key Responsibilities
- Support the compilation, submission, and approval of Country Specific Submissions files for responsible countries.
- Review and provide input on labelling materials and promotional materials as required.
- Update local requirements based on regulatory agencies' guidance and input from affiliates/distributors.
- Manage working relationships with key stakeholders.
Requirements
- Graduate/Postgraduate in pharmacy, science, or a relevant field.
- 5+ years of work experience within relevant Regulatory Affairs qualifiers.
- Fluent in written and spoken English.
- Excellent knowledge of Pharmaceutical Regulatory overview: Regulatory guidelines & landscape, Regulatory IT systems & tools.
About the Department
You will be part of our GBS team in Mexico City, working in a dynamic and collaborative atmosphere. Our team is dedicated to supporting our global operations and ensuring compliance with regulatory standards.
Working at Novo Nordisk
We are a dynamic company in a dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We strive for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. Working at Novo Nordisk is working toward something bigger than ourselves, and it's a collective effort.
Contact
To complete your application, please click on "Apply now" and attach your CV. For more information, please visit our website.
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