
Regulatory Affairs Expert
Há 8 horas
We are seeking a skilled Regulatory Affairs Associate Director to lead our biopharmaceutical regulation process, ensuring seamless compliance with target country legislation and efficient execution.
This role will play a pivotal part in supporting our global strategy on regulatory matters, fostering collaboration across functional teams, and promoting the strategic direction of our organization.
The successful candidate will possess expertise in building new capabilities, driving cross-functional collaboration, and overseeing procedures for biopharmaceuticals. Additionally, they will support our efforts in providing reliable, compliant medical products, practices, and solutions worldwide.
We value professionals who can think strategically, drive innovation, and promote organizational excellence. If you have experience in regulatory affairs, enjoy collaborating with international teams, and are passionate about healthcare breakthroughs, we encourage you to apply for this exciting opportunity.
Key Responsibilities:
- Oversight of the biopharmaceutical regulation process, ensuring timely and compliant execution.
- Supporting our global strategy in regulatory matters, fostering collaboration, and promoting strategic direction.
- Building new capabilities and leading cross-functional teams to drive organizational excellence.
- Providing expertise in regulatory affairs, enabling the development of reliable, compliant medical products and solutions.
Benefits:
- Opportunity to work in a dynamic, international environment, driving healthcare innovation and excellence.
- Chance to develop your skills and expertise in regulatory affairs, working closely with experienced professionals.
- Collaborative team culture, encouraging open communication, and knowledge sharing.
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