Regional Regulatory Affairs Senior Associate
Amgen
- Lisboa
- Permanente
- Horário completo
- Execute the regional regulatory strategy and regional regulatory plans.
- Prepare supportive documentation for regulatory deliverables, including the management of clinical trial applications, marketing authorizations, and lifecycle management activities.
- Use of Amgen systems and document management.
- Ensure and support regulatory product compliance.
- Work with Policies and SOPs.
- Build effective relationships and communication paths across local and functional organizations.
- Enable efficiencies and seamless execution across the region countries.
- Master’s degree (scientific area) OR Bachelor’s degree (scientific area) and 2 years of directly related experience.
- Degree and in-depth regulatory experience and/or related to the region.
- Depth knowledge of regional countries legislation and regulations relating to medicinal products.
- Vast opportunities to learn, develop, and move up and across our global organization.
- Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.
- Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth and career benefits.
- Flexible work arrangements.