Associate Regulatory Affairs

Amgen

Live

What you will do

Let s do this. Let s change the world. In this vital role, you will manage country-specific regulatory affairs for Amgen's molecules, coordinate and implement regulatory submissions, ensure compliance with corporate and local requirements and lead documentation for local submissions under Senior Manager's guidance :

• Ensures regulatory submissions are made on time and meet Amgen s corporate and local regulatory requirements

• Local coordination and execution of regulatory submissions in compliance with corporate standards and local regulatory requirements.

• Execution of the preparation, delivery, and electronic archiving of documentation for inclusion in local regulatory submissions.

• Coordination and execution of Regulatory Affairs processes and deliverables in the local office.

• Reviews promotional and non-promotional materials

• Exchanges regulatory information and intelligence with other regulatory colleagues and cross functional teams on an ongoing basis and provides advice on local regulatory considerations/regulations in a timely manner

• Partners with international Regulatory Leads (IRL) to support the regulatory development, registration, and lifecycle management of all Amgen molecules

• Partners with peers to ensure consistency on procedures

• Assists locally in Healthcare Compliance activities, where applicable

• Participate in local regulatory process improvements, initiatives, and training

• Overseas external vendor/contractor relationships, where applicable

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The Associate Regulatory Affairs professional we seek is a teammate with these qualifications.

Basic Qualifications:

• Bachelor`s degree in Pharmaceutical Science

• Knowledge of Regulatory Principles

• Working with policies, procedures and SOP s

• Comprehensive understanding of regulatory activities and how they impact other projects and/or processes

• Understanding of drug development

• Demonstrate ability to work in teams

• Ability to understand and communicate scientific/clinical information

Preferred Qualifications:

• Regulatory experience of the Gulf Markets (1 year experience)

• Knowledge of legislation and regulations relating to medicinal products in the Gulf Markets.

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.

In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com