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:

Up to CHF62 per hour

Location:

Switzerland

Description

Hobson Prior are looking for a Regulatory Project Manager to join a world-wide pharmaceutical company based in Switzerland.

Salary:

£45000 - £55000 per annum

Location:

Nottingham, Nottinghamshire

Description

Hobson Prior are looking for a Regulatory Affairs Manager to join a leading pharmaceutical organisation to join them on a permanent basis in Nottingham.

Salary:

€95000 - €100000 per annum

Location:

Austria

Description

Hobson Prior are looking for a Regulatory CMC Manager to join a leading pharmaceutical organisation who are focused on developing and offering therapy options

Salary:

£600 - £650 per day

Location:

Welwyn Garden City, Hertfordshire

Description

Hobson Prior are recruiting for Senior Initiative Project Manager (Regulatory) to join a multinational healthcare company at their offices in Hertfordshire.

Salary:

£100000 - £150000 per annum

Location:

London

Description

Hobson Prior are working with a clinical-stage biopharmaceutical organisation, who currently have an exciting opportunity for an experienced CMC Regulatory Affairs Director

Salary:

Up to £51 per hour

Location:

High Wycombe, Buckinghamshire

Description

Hobson Prior are looking for a Senior Regulatory Affairs Associate to join a leading healthcare organisation on a contract basis in High Wycombe.

Salary:

€75 - €90 per hour

Location:

Marburg (35037), Hessen

Description

Hobson Prior are looking for a Regulatory Labelling Consultant to join a top Biotechnology organisation who specialise within Rare Diseases.

Salary:

£30 - £35 per hour

Location:

Hoddesdon, Hertfordshire

Description

Hobson Prior are looking for a Senior Regional Associate Regulatory Affairs to join a leading global biopharmaceutical company that has been inventing for life for more than a century.

Salary:

€55 - €60 per hour

Location:

Brussels

Description

Hobson Prior currently have an opportunity for an Associate Liaison Regulatory Affairs to support Regulatory Affairs activities

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