Expiry Date: 03-11-2022
Categories Biotech, Regulatory Affairs
Salary: On Application
Job Type: Full Time
The cell therapy product pipeline of this client is rated as one of the strongest and most in-depth in the industry, and they have already been successful in bringing several Cell Therapy products to market (EU & US). They are now recruiting for Regulatory Affairs CMC Director, experienced in Cell or Gene Therapy.
As the Director of Global Regulatory CMC for Cell Therapy you will be responsible for both people and global projects, representing Regulatory CMC matrix teams for the cell therapy commercial products team, leading global submissions and major US and EU variations.
There is full flexibility to work remotely, or you can be in a hybrid role mixing home and office working from any of their 7 locations based on the East or West Coast.
The role reports into an engaging Executive Director who has been working in the ATMP space for over 10 years, with several notable registrations and achievements under their belt.
In return for leading both people and global projects, my client is offering high-end packages including an industry high basic salary, lucrative bonus and extremely generous RSU plan. They will also look at offering a bonus to cover any loss of stock (when you leave) and will cover a loss of a proposed bonus for 2023.
For more information, in the first instance please contact me, Theo Moore on US +1-908.348.6714 or via email at Theo@Advtalent.com and I would be happy to discuss the role further and give you more information.
If this role isn’t quite for you but you are open to something new, I would be happy to discuss other roles we have open.
To apply for this role, please contact me Theo Moore on US 908.348.6714 or press the red “Apply for position” button. I will support you throughout the interview and on-boarding process!
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