Job Description
Principal Consultant (CMC, small molecules experience)
Scendea is seeking a highly motivated individual to join our global team as a full‑time Principal Consultant. The ideal candidate will have a proven track record in CMC for small molecule drug development, with expertise in process development, scale‑up, regulatory submissions, and the pre‑approval life cycle management of small molecule products. This is a hybrid position, affiliated to either our UK or Australia office, with a requirement to work in the office a minimum of one day per month.
This is an excellent opportunity to progress your career at a rapidly growing regulatory consultancy. You will have the opportunity to play a key role in the development and mentoring of staff whilst providing high‑quality regulatory technical advice and product development strategies for clients.
Requirements
Role Requirements
- Provide strategic, technical and regulatory advice/service...
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