12 set - Follonica
NNIT
UK, Denmark, Italy, Germany, Poland, Czech, Ireland, Switzerland
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Details
Type of contract: Permanent
Location(s): UK, Denmark, Italy, Germany, Poland, Czech, Ireland, Switzerland
Language(s): English
Mobility: Some Travel
Application Deadline: 30/10/2026
Senior Consultant - Regulatory Affairs
NNIT is one of the world’s leading consultancies for the past twenty years serving the Life Science industry around the world. We strive to enable our customers to achieve their business goals through digitalization within Quality Assurance, Regulatory Affairs, Clinical, Pharma Production and Laboratory processes.
To further strengthen our Regulatory Affairs team, we are looking for a Senior Consultant with a diverse skill set across Regulatory Affairs in the life sciences industry including some IDMP regulatory affairs exposure.
Your Responsibilities
You will join our Regulatory Affairs team as a Senior Consultant.
You will contribute to forming a variety of tasks and functional responsibilities within the Regulatory Affairs business unit such as taking ownership of client engagements and specific projects, contribute to business development and sales activities and contribute to and deliver Requests for Proposal (RFP’s) as required.
On Average You Will Split Your Time
- 75% delivering in consultancy projects in advisor, project lead or architect roles, and acting as engagement delivery lead.
- 10% in business development, presales and though leadership activities
- 10% in the development and delivery of RFP’s to ensure NNIT successfully engages new and additional projects
- 5% in coaching and mentoring of more junior consultants in the Regulatory Affairs team
Essential Requirements
Your qualifications and experience:
- A Bachelor’s Degree (or similar) in a field related to Pharmaceutical Compliance or Regulation. Other relevant academic qualifications can be considered if you also have highly significant consulting and/or industry based experience in
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