Global Regulatory Affairs Intercontinental
vor 2 Wochen
**Responsibilities**:
- Plan, direct, and monitor regulatory affairs activities so the organization has the permits, licenses, certificates, authorizations, and other approvals needed to conduct current and future business activities; and produce, sell, and distribute its goods and services.
- Support development of consistent roles and work processes.
- Oversee development of plans, cost estimates, and schedules.
- Acquire the necessary permits and approvals.
- Monitor regulatory developments and advise management on the potential impact of regulations on the organization.
- Establish and maintain positive relationships with government agencies and other regulatory authorities.
- Represent the organization in matters before regulatory, legislative, or industry standards agencies so the organization's interests are advanced.
- Prepare materials for legal counsel or external consultants.
- Regulatory system, data entry and maintenance in/of regulatory systems.
**Qualifications**:
- Bachelor degree in a Life Science or Business Advanced degree in a Life Science (PhD, MD) or Business (MBA) an advantage.
- 3+ years regulatory experience in the pharmaceutical industry. Biologics Regulatory experience preferred.
**Our Benefits**:
We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.
**About CSL Behring**:
CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.
**We want CSL to reflect the world around us**:
As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.
**Do work that matters at CSL Behring**:
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