Description
A global pharmaceutical organisation is looking for a Regulatory Affairs Consultant for a part time contract / freelance role based in Netherlands.You will be required to spend 10/15% - Onsite and the rest (85/90%) will be remote working
Tasks:
* Write / Compile - Dossier for New Product Application
* Liaise with internal stakeholders for dossier creation
* Liaise with local / national authorities to ensure regulatory requirements are met.
* Product type - Small Molecules.
Knowledge:
* Experience of Pre Approval
* Experience with respect to interaction with health authorities
* Demonstrated knowledge of regulations related to new product introduction, quality and GMP.
* Able to create, compile and write dossier for submission.
Language Skills:
* English only or Dutch / English consultant.
This a part time contract opportunity starting 1st of September. We are offering competitive rates of pay; please apply now for more information!