Skip to main content

This job has expired

Principal Regulatory Consultant

Employer
Barrington James
Location
Netherlands
Salary
Competitive
Start date
3 Dec 2024
Closing date
1 Jan 2025
View more categoriesView less categories
Discipline
Regulatory Affairs, Compliance
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Job Description

Are you an experienced regulatory professional ready to take the lead in shaping innovative CMC strategies? Barrington James is recruiting for a Principal/Senior Consultant (CMC) to join a dynamic and growing global consultancy. This is a hybrid role based in Breda, Netherlands, with a flexible schedule and monthly office visits. If you're passionate about guiding clients through complex regulatory landscapes while mentoring the next generation of experts, we want to hear from you!

*Minimum of 8 years experience required*

In this role, you'll provide strategic and technical regulatory advice to clients, focusing on CMC (Chemistry, Manufacturing, and Controls) aspects of product development. You'll also oversee regulatory submissions, guide multi-jurisdictional projects, and manage client relationships. Additionally, you'll play a key role in mentoring junior team members and contributing to business development efforts.

Responsibilities
  • Develop innovative CMC regulatory strategies, gap analyses, and drug development plans.
  • Lead the preparation, authoring, and review of regulatory documents (INDs, IMPDs, MAAs, etc.).
  • Represent clients in regulatory agency interactions, addressing objections and negotiating outcomes.
  • Oversee project timelines, budgets, and deliverables, ensuring high-quality outcomes.
  • Mentor and manage team members, providing training and technical leadership.
  • Contribute to business development through client relationships and identifying new opportunities.
  • Stay ahead of regulatory trends and ensure compliance with evolving standards.


Requirements
  • Senior Consultant: 8+ years in drug development and regulatory affairs.
  • Principal Consultant: 10+ years in drug development and regulatory affairs.
  • Proven experience with FDA, EMA, and/or MHRA processes, including submissions and negotiations.
  • Expertise in biologics, ATMPs, vaccines, or small molecules.
  • Advanced degree in life sciences (MSc or PhD preferred).
  • Strong leadership, organizational, and time management skills.
  • Willingness to travel occasionally and work flexible hours.


To apply:

kwilson@barringtonjames.com

Direct line: +44 1293 223 951

Company

We’re great at what we do. A collection of the worlds finest Life Science recruiters working for the worlds best Life Science consultancy.

Originally, a purely contingency and contract recruiter, focused in the UK, Barrington James is now a sophisticated, highly effective provider of human resources solutions up to full RPO, partnering the pharma, medical devices, and healthcare industries right across the globe.

Company info
Website
Telephone
01293 776644
Location
The Galleria
Station Road
Crawley
West Sussex
RH10 1WW
United Kingdom

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert