Deputy Head of Product Development – international Scope

Location:

Netherlands

Salary:

Negotiable

Type:

Permanent

Main Industry:

Search Health, Nursing & Social Services Jobs

Advertiser:

NonStop Consulting

Job ID:

131938350

Posted On: 

23 May 2025

Deputy Head of Product Development & Regulatory Consulting
Senior/Principal Consultant Level | Hybrid – UK, Netherlands, or Australia

A fast-growing international consultancy is seeking a highly motivated individual to join its leadership team as Deputy Head of Product Development & Regulatory Consulting. This is a full-time hybrid position, reporting to the Head of the department, with affiliation to one of the company’s offices in the UK, Netherlands, or Australia (minimum one day per month on-site).

This is an exciting opportunity to play a pivotal role in leading regulatory consulting operations, delivering strategic advice to clients, and mentoring a high-performing team of consultants.

x1F539; Key Responsibilities

Support the Head of Department in leading the global operational team and driving delivery excellence
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Provide regulatory and technical strategy support for early development through to marketing authorisation
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Oversee and contribute to the preparation of regulatory documentation including INDs, CTAs, MAA/BLAs, and more
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Lead multi-jurisdictional projects and ensure quality, budget, and timeline adherence
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Line-manage, mentor, and coach a team of consultants, fostering their professional development
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Collaborate with business development to grow client accounts and support proposal efforts
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Contribute to internal process improvements, systems implementation, and SOP development
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Participate in leadership activities and contribute to overall business strategy and direction

x1F539; Required Skills & Experience

Advanced scientific qualifications (MSc/PhD in Life Sciences or related field preferred)
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8+ years of drug development and regulatory experience for Senior Consultant level, or 10+ years for Principal Consultant level
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Regulatory experience with authorities such as the FDA, EMA, MHRA, or TGA, including agency interactions
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Strong leadership background with 5+ years of direct or matrix management experience
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Broad therapeutic area knowledge and proven ability to provide strategic development advice
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Excellent writing, project leadership, and client-facing communication skills
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Strong commercial awareness and ability to contribute to account growth
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Proficiency in Microsoft Office; ability to travel when required

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