Company

Barinthus BiotherapeuticsSee more

addressAddressDidcot, Oxfordshire
type Form of workFull Time
salary Salary£100,000 to £150,000
CategoryScientific

Job description

Job Details

Senior Director or Director of Regulatory Affairs Strategy

Location: Harwell, UK

Hybrid Working - 3 days onsite, 2 days working from home

Salary Range: £100,000 to £150,000

 

Barinthus Biotherapeutics is on a quest for a Senior Director or Director of Regulatory Affairs Strategy who is not just looking for a job, but a calling. With us, you’ll embark on a journey of discovery, guiding the immune system to conquer chronic diseases, autoimmunity, and cancer.

 

What’s in it for you?

 

  • Be a Trailblazer: Be part of a rapidly growing business that’s reshaping the healthcare landscape.
  • Flexible Work-Life Balance: Enjoy our flexible working policy, with the option to work from home for up to two days per week.
  • Empowering Benefits: From pension plans to healthcare, and share options, we invest in your future.
  • Innovative Culture: Work in an environment that values Leading By Example, is Team FocusActing With Impact, and upholds Trust and Respect all to Deliver Excellence.

 

What you’ll be doing:

 

  • Strategize for Success: Lead the global regulatory strategy for our cutting-edge immunotherapeutic products.
  • Drive Regulatory Excellence: Manage strategic regulatory documents and interactions with global agencies.
  • Collaborate for Impact: Align regulatory strategies with product development plans, working with diverse teams.

 

Essential skills and requirements:

 

  • Biologics Regulation Expertise: Experience in the regulation of biologics, including immunomodulating therapies and vaccines, is highly valued.
  • Product Development Insight: In-depth experience with clinical and non-clinical regulatory aspects of products in development.
  • Global Regulatory Knowledge: Strong experience with biologics registration requirements in Europe and familiarity with international regulations (UK MHRA essential, US FDA preferred).
  • Regulatory Lifecycle Proficiency: Solid understanding of Regulatory Life Cycle Management and eCTD format for regulatory filings.
  • Submission Mastery: Demonstrated ability in drafting and organizing regulatory submissions, amendments, and supplements.

 

The Time to Act is Now! Don’t miss this chance to make a real difference. Apply today and join a team that’s not just part of the industry, but leading it. Barinthus Biotherapeutics is more than a company—it’s a beacon of hope and innovation. Apply now and let’s navigate towards a healthier world together.

 

Barinthus Biotherapeutics awaits your expertise. Are you ready to guide us into the future? Apply now and let your career set sail with us.

 

** To request a full job description please email recruitment@barinthusbio.com **

Refer code: 3342435. Barinthus Biotherapeutics - The previous day - 2024-05-15 16:43

Barinthus Biotherapeutics

Didcot, Oxfordshire
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