Lead Global Regulatory Affairs Operations for Enhanced Productivity
vor 2 Wochen
We are seeking a highly experienced and skilled Director to lead our Central Services Group, responsible for enhancing productivity through simplified and harmonized processes. The successful candidate will oversee the global CSG team, ensuring seamless coordination of all submissions related to CSL Vifor, Seqirus, and Behring product portfolios.
About the Role- Pivotal in shaping GRA's ability to deliver efficiently and timely worldwide submissions by assembling a high-performing CSG team.
- Continuously seek efficiency gains by exploring new ways of working and operating.
The ideal candidate will have 15+ years' experience in the pharmaceutical industry and Global Regulatory Affairs, with expertise in dossier preparation, regulatory affairs processes, and compliance matters. A master's degree in Life Science or Business is required, along with strong leadership skills and experience in building high-performing teams.
Requirements- Advanced degree in Life Science or Business.
- 15+ years' experience in the pharmaceutical industry and Global Regulatory Affairs.
- Experience with Veeva RIM Suite appreciated.
- 10+ years' leadership experience with global regulatory teams.
- Fluent in English.
As a valued member of our team, you will enjoy a competitive salary of $150,000 - $200,000 per year, depending on your level of experience. You will also be entitled to a comprehensive benefits package, including health insurance, retirement savings plan, and paid time off.
About UsCSSLimited is a global biotechnology company dedicated to developing and delivering innovative medicines that treat rare and serious diseases. Our products offer promise for patients in over 100 countries, and we are committed to making a positive impact on their lives. At CSL Behring, we value diversity, inclusion, and collaboration, and we are passionate about creating a workplace where everyone can thrive.
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