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:

CHF110 - CHF120 per hour

Location:

Zürich

Description

Hobson Prior are looking for a Regulatory Affairs Senior Manager to join a very patient focused worldwide biopharmaceutical organisation located in Zurich.

Salary:

£55 - £60 per hour

Location:

Cambridge, Cambridgeshire

Description

Hobson Prior currently have a 12-month contract opportunity for a Manager Regulatory Affairs CMC to join the Regulatory Affairs Team

Salary:

€25 - €32 per hour

Location:

Brussels

Description

Hobson Prior are looking for a XEVMPD Submission Support to manage the submissions of medicinal product information

Salary:

CHF70 - CHF90 per hour

Location:

Basel

Description

Hobson Prior are currently seeking a Technical CMC Manager Regulatory to join a Swiss global healthcare organisation

Salary:

£85000 - £100000 per annum

Location:

Slough, Berkshire

Description

Hobson Prior are looking for a Director of Regulatory to join a leading pharmaceutical organisation in Slough.

Salary:

CHF110 - CHF120 per hour

Location:

Zürich

Description

Hobson Prior are looking for a Regulatory Affairs Associate Director - Rare Disease to join a very patient focused worldwide biopharmaceutical organisation located in Zurich.

Salary:

£85 - £90 per hour

Location:

Basel

Description

Hobson Prior are currently seeking a Technical Regulatory Specialist to join a Swiss global healthcare organisation

Salary:

CHF95 - CHF100 per hour

Location:

Zürich

Description

Hobson Prior are looking for 3 Regulatory Affairs Senior Manager to join a very patient focused worldwide biopharmaceutical organisation located in Zurich.

Salary:

£90000 - £102000 per annum

Location:

Slough, Berkshire

Description

Hobson Prior are looking for a Head of Labelling to join a leading biopharmaceutical company on a contract basis in Slough.

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