Requirements
Apotech is looking to bring on a Regulatory Affairs Consultant with a specific focus on MDR, to service our clients across Europe and the US.
- Experience with MDD to MDR remediation projects for medical devices
- Experience with Technical writing and reviewing technical documents
- Knowledge of design and risk control processes within a Medical Device Company QMS
- Experience in reviewing sterilisation and biocompatibility documents for medical devices would be an advantage
- Excellent organisation and communication skills required
- Must be able to work off own initiative and be solution-focused