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:

£15 - £19 per hour

Location:

Uxbridge, London

Description

Hobson Prior are working with a leading independent biotech organisation who are looking for a UK Junior Regulatory Affairs Associate

Salary:

CHF90000 - CHF95000 per annum

Location:

Geneva

Description

Hobson Prior are seeking a Bioanalytical Research Associate/Scientist to join a drug discovery and development company who concentrates on developing antibody-based drugs

Salary:

€60 - €80 per hour

Location:

Frankfurt am Main, Hessen

Description

Hobson Prior are looking for a Regulatory Labelling Manager to join a leading science and technology organisation who aim to help and prolong life.

Salary:

£30 - £32 per hour

Location:

Uxbridge, London

Description

Hobson Prior are looking for a Senior Regulatory Affairs Associate to join a research-based biopharmaceutical organisation

Salary:

£37.84 - £44.15 per hour

Location:

Gothenburg

Description

Hobson Prior currently have an opportunity for a Senior CMC Documentation Lead to join a Regulatory Documentation Team at a research-based biopharmaceutical organisation

Salary:

€35 - €40 per hour

Location:

Brussels

Description

Hobson Prior is currently seeking a Regulatory System Support - Submission Planning and Content Management for a leading global biopharmaceutical company

Salary:

€50000 - €55000 per annum

Location:

Jena, Thüringen

Description

Hobson Prior are working with a leading pharmaceutical company who specialise in developing pioneering products for the treatment of structural heart disease.

Salary:

€45 - €50 per hour

Location:

Belgium

Description

Hobson Prior are looking for a Regulatory Affairs Senior Associate to join a top pharmaceutical organisation who are focused on delivering innovations that transform patients lives.

Salary:

£52 - £57 per hour

Location:

Cambridge, Cambridgeshire

Description

Hobson Prior are currently working with a global biotechnology organisation who are seeking a UK CW Regulatory Affairs Manager to join them on a contract basis in Uxbridge or Cambridge.

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