Regulatory affairs recruitment solutions

In order for a pharmaceutical, biotechnology of medical device’s product to go to market, it requires the appropriate licensing in line with national and international regulations. With compliance, documentation and changing legislations such as EU MDR and IVDR implementation, an experienced and effective regulatory affairs team is key.

Our network contains professionals from around the world with expertise in authoring and submitting applications to achieve approvals from health authorities such as MHRA, EMA, FDA and SwissMedic.

The changes to the EU medical device regulations and in vitro diagnostics regulations has been called the most disruptive change in recent industry history. Hobson Prior is helping medical device manufacturers prepare their teams by arming them with skilled professionals that will help them minimise risk and ensure compliance to the regulations by 2020.

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  • Development
  • Post-Marketing(GCP)
  • CMC
  • Labelling
  • Operations
  • Marketing Authorisation
  • CTD Authoring
  • EU MDR preparation

Our Regulatory Affairs Team

Raymond Pankhurst

Lead Regulatory Affairs Recruiter

01892 337 408

Francesca DeNieffe

Regulatory Affairs Recruiter

01892 337 411

Hani Moussalli

Regulatory Affairs Recruiter

01892 337 409

Regulatory affairs specialists are in constant demand throughout the life sciences industry, for trialling new drugs and devices, bringing them to market or maintaining their licenses

We specialise in finding professionals with the specific experience and skill sets that match our clients’ regulatory requirements. Our dedicated RA team works across the pharmaceutical, biotech and medical devices sectors, providing specialist staff for clinical trial applications, marketing applications (MRP, DCP, CP) through to life cycle management, CMC, labelling and artwork, regulatory operations, CE marking and 510K.

Our RA team has an exceptionally strong network of high-quality candidates across the regulatory arena, many of who choose to work with us exclusively and can't be easily found by other recruiters.

Latest jobs

Salary:

£110000 - £135000 per annum

Location:

Slough, Berkshire

Description

Hobson Prior are looking for a Global Regulatory Leader - Medical Devices to strengthen the Global Regulatory Affairs department at a leading biopharmaceutical company

Salary:

£65000 - £75000 per annum

Location:

Berkshire

Description

Hobson Prior currently have the opportunity for a Senior Regulatory Project Manager to join a world-wide life science organisation who are dedicated to ground-breaking

Salary:

CHF100000 - CHF115000 per annum

Location:

Bonaduz, Imboden

Description

Hobson Prior are looking for a Risk Management/Regulatory Specialist (Device role) to join a top pharmaceutical organisation focused on

Salary:

£30 - £32 per hour

Location:

Uxbridge, London

Description

Hobson Prior are working with a leading biotechnology organisation who are dedicated to putting innovative ideas and discoveries into medicines

Salary:

£950 - £1000 per day

Location:

Macclesfield, Cheshire

Description

Hobson Prior are looking for a Regulatory CMC Lead to join a leading biopharmaceutical organisation who provide pioneering medicines to patients all over the world.

Salary:

£90000 - £110000 per annum

Location:

Slough, Berkshire

Description

Hobson Prior are looking for a Regional Regulatory Affairs, UK Liaison Associate Director for an exciting opportunity to join a leading

Salary:

€35 - €70 per hour

Location:

London

Description

Hobson Prior are working with a Global CRO who are seeking a Regulatory Affairs Consultant for MA Transfer be home-based in Europe on a contract basis.

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