At a Glance
- Tasks: Provide strategic regulatory guidance and lead projects in CMC development for small molecules.
- Company: Join Scendea Ltd., a global leader in pharmaceutical consulting.
- Benefits: Enjoy a hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Be part of a dynamic team driving regulatory success for clients worldwide.
- Why this job: Make a real impact in drug development while mentoring a talented team.
- Qualifications: Extensive experience in CMC, regulatory compliance, and drug development required.
The predicted salary is between 63000 - 77000 £ per year.
Scendea Ltd. is seeking a highly experienced Principal Consultant (CMC, small molecules) to join our global team in a hybrid role, UK or Australia office. The candidate will provide strategic regulatory guidance for CMC development of small molecule medicines, lead multi-jurisdiction projects, and mentor the Scendea team while driving regulatory success for clients.
The role requires a strong background in CMC, regulatory compliance, and drug development, with extensive experience.
CMC Small Molecules Principal Consultant employer: Scendea Ltd
Scendea is an exceptional employer that fosters a collaborative and innovative work culture in the heart of Bishop's Stortford. With a strong commitment to employee growth, we offer comprehensive coaching and mentoring opportunities, alongside competitive benefits such as private healthcare and a generous holiday allowance. Join our dynamic team and contribute to meaningful healthcare advancements while enjoying a supportive environment that values your professional development.
