Director or Senior Director

Barinthus Biotherapeutics

Director or Senior Director

£150000

Barinthus Biotherapeutics, Didcot, Oxfordshire

  • Full time
  • Permanent
  • Remote working

Posted 2 weeks ago, 17 May | Get your application in now before you miss out!

Closing date: Closing date not specified

job Ref: 86e388f877e842d5b6c192e4827d5d54

Full Job Description

Senior Director or Director of Regulatory Affairs Strategy Location: Harwell, UK Hybrid Working - days onsite, 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, youll embark on a journey of discovery, guiding the immune system to conquer chronic diseases, autoimmunity, and cancer. Whats in it for you? Be a Trailblazer : Be part of a rapidly growing business thats 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 Focus , Acting With Impact , and upholds Trust and Respect all to Deliver Excellence. What youll 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 Dont miss this chance to make a real difference. Apply today and join a team thats not just part of the industry, but leading it. Barinthus Biotherapeutics is more than a companyits a beacon of hope and innovation. Apply now and lets 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.