Expiry Date: 06-11-2021
Category Regulatory Affairs
Job Type: Full Time
Windsor and Maidenhead
Associate Director Global Regulatory Affairs CMC Biologics in mid to late stage of development (mAbs), file a new MAA/BLA with a growing R&D based company.
Consolidate your EU and US Regulatory CMC experience. File initial MAA/BLAs.
This is an opportunity to join an already successful biopharmaceutical company at a pivotal stage of their history. With a diverse and busy pipeline, several major MAA/BLAs planned in the coming years, 2 business acquisitions recently adding to the pipeline, as well as billions of euros planned in reinvestments in R&D, this company offers great career opportunities.
Why consider this role?
We are seeking an individual who can thrive in this environment and wants to work in a company which is growing and has a successful track record in developing and registering molecules.
This is an opportunity for you to consolidate and develop your Regulatory CMC career is a merit-based company where empowerment and promotions are encouraged.
Package & Benefits
This company offers a competitive salary, including a bonus and a share plan as well as other benefits. The company is willing to consider individuals that want to work from home for 2 days per week post Covid-19 (currently you can work from home).
To apply for this role, please press the red “Apply for position” button, or contact Oli Dimitrov on +44 (0)207 801 3388 or Theo Moore on +44 (0)207 801 3384 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.
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