Director of Global Regulatory Affairs and Product Development
3 weeks ago
At Genmab, we're committed to pushing the boundaries of innovation in the development of antibody products and pioneering therapies for cancer treatment and serious diseases.
The role you'll be playing is pivotal in driving our vision forward. As a Director of Global Regulatory Affairs and Product Development, you will be responsible for overseeing operational and strategic regulatory input to support worldwide development and commercialization.
We're seeking an experienced professional with a strong understanding of compliance and biologics, as well as a track record in moving therapeutic products through various stages of development. Your expertise in preparation of BLAs and lifecycle management will be invaluable in this role.
In collaboration with cross-functional peers, you will facilitate and optimize product development, plan, review and prepare CMC documentation, and provide advice and guidance on EU, US, and selected worldwide regulatory legislation for CMC topics.
A salary range of 120000 - 160000 USD per year, depending on experience, reflects the level of expertise required for this position. The compensation package also includes benefits such as health insurance, retirement plans, and opportunities for career growth.
This dynamic, global company offers a collaborative work environment where talented colleagues in Regulatory Affairs and within Genmab's CMC organization come together to foster a culture of mutual support and open communication. Our agile working environment prioritizes employee work-life balance, allowing you to thrive both personally and professionally.
Genmab's commitment to diversity, equity, and inclusion ensures that all applicants are treated fairly without bias. We protect your personal data and privacy, adhering to strict policies to safeguard your information.
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