Regulatory Affairs Lead – South East of the UK

Moin Din at CK Clinical is recruiting for a Regulatory Affairs Lead – Devices to join a leader in the manufacture and supply of specialty pharmaceuticals at their site based in the South East of the UK.

The Company:

If you are successful for this Regulatory Affairs Lead role you will join an award winning organisation that has been formally recognised as one of the fastest growing companies in 2012.

They are now looking to expand into new and exciting areas and are seeking a well versed and dynamic individual with experience in Regulatory Affairs for medical devices at a national, European and International level to take them to the next stage.

Responsibilities:

As a Regulatory Affairs Lead you will report to the Director of Regulatory and Medical Affairs, as such you will be experienced in class II and class IIIb medical devices.  You will be highly proficient at working with most regulatory bodies and possess good knowledge of CE mark.

This role is not just about existing products, you will also be involved in developments in new areas and on going clinical trials that will form the basis of further expansion and growth and will lead the submission of all new product applications.

  • Be responsible for the maintenance and renewal of CE marks for all Class IIb and III Medical Devices within the company’s existing Business Segments
  • Cross-business expert in Medical Devices from a regulatory perspective, able to shape and assist other functions as they build and strengthen the company medical devices portfolio
  • Maintain and develop CE mark for the company’s wound dressing range – have commercial focus to position the products in the right place in the market
  • Lead the CE mark filing and approval for company’s novel wound care products in Europe
  • Obtain all relevant regulatory approvals for company’s novel wound care products in key International markets.

This role is not just about existing products, you will also be involved in developments in new areas and on going clinical trials that will form the basis of further expansion and growth and will lead the submission of all new product applications.

Qualifications, Skills and Experience:

To be considered for this Regulatory Affairs Lead role, you will have the following qualifications, skills and experience:

  • A full-range of Regulatory experience in class II and IIIb devices
  • Highly proficient at working with most regulatory bodies and possess good knowledge of CE mark.
  • Experience in successful European and International Registration (class IIb and III devices)
  • A strong understanding of the business and commercial awareness.
  • Have experience of managing and maintaining excellent relations with the various Regulatory Authorities in Europe and internationally
  • 6-8 years regulatory experience gained in an international medical devices environment, ideally with experience in wound care
  • A philosophy that sees Regulatory Affairs as a value-adding, integral part of the business, rather than a bureaucratic “necessary” function
  • Accustomed to interacting effectively at all levels within the organisation, as well as with regulatory authorities and external partners/distributors

This is an amazing prospect for the right person seeking their next career move. If you have solid experience in Regulatory affairs class II and IIIb devices, don’t miss this opportunity.

Moin Din - Senior Recruiter at CK ClinicalHow to Apply:

Apply online:

For an informal discussion and further information regarding this Regulatory Affairs Lead role please contact Moin Din in the first instance on +44 (0)207 470 5675 or email on mdin@ckclinical.co.uk.  Please quote reference CL25031 in all correspondence.

Are you looking for a new Medic role within the Pharmaceutical, CRO, Biotechnology and Healthcare industries?

Click here to see our latest Medic jobs

Posted in Featured Jobs, Industry News, NewsTagged in , , , , , , , , , , , , , , , , , , , ,

Medic Jobs in the Pharmaceutical Industry

Moin Din at CK Clinical is currently recruiting for a number of Medic positions in the UK pharmaceutical industry.

 

Please click on the links below to find out more and apply online now:

 

Medical Advisor – South East, UK

 

Associate Director of PV – South East, UK

 

Interim Head of Medical Affairs – UK

 

Senior Medical Advisor – UK

 

Medical Director – UK

 

Medical Affairs Manager – South East, UK

 

 

Contact Moin:

Moin Din - Pharmaceutical Physician Recruitment at CK Clinical

Please contact MOin for more details.

For more information regarding medically qualified positions within the pharmaceutical industry in the UK and across Europe, please contact Moin Din on +44 (0)207 470 5670 or email info@ckclinical.co.uk.

 

 

Register your CV

Click here to register your CV online now.

Once your CV has been registered, one of our specialist pharmaceutical Recruitment Consultants will be in contact with you to discuss your requirements and any Physician jobs we are currently recruit for.

Posted in Featured Jobs, NewsTagged in , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,

Meet Moin Din – Medics Recruitment at CK Clinical

Meet Moin Din, Senior Recruitment Consultant at CK Clinical. Moin specialises in recruiting for Medics and senior level appointments within the Pharmaceutical, CRO, Biotechnology and Healthcare industries.

Moin covers all permanent, interim and contract recruitment within CK Clinical’s Medic Recruitment function. To find out more, please watch Moin’s short video below:

Looking for a Medic job in the Pharmaceutical Industry?

Click here to search our current medic jobs online now.

Alternatively, please call us on +44 (0)1438 743 047 or email info@ckclinical.co.uk.

Click here to meet the rest of the CK Clinical recruitment team.

Posted in company news, NewsTagged in , , , , , , , , , , , , , , , , , ,

CK Clinical to Exhibit at the DIA EuroMeeting in Copenhagen

CK Clinical, the specialist UK and EU pharmaceutical recruitment consultancy, is proud to announce that we will exhibiting on stand 714 at the 2012 DIA (Drug Information Association) 24th Annual EuroMeeting 2012.

About the EuroMeeting 2012

The EuroMeeting which is taking place 26th to 28th March at Copenhagen, attracts more than 3,000 professionals from over 50 countries. It brings together professionals from the biopharmaceutical industry, contract service organisations, clinical research, regulatory agencies, health ministries, patients’ organisations and universities. The EuroMeeting also offers:

  A neutral, global forum featuring over 120 sessions attracting
more than 3,000 professionals involved in the development of
medicines from more than 50 countries
•  Speakers from the European Medicines Agency, the European
Commission, the FDA and other regulatory agencies from
European countries and other regions of the world
•  More than 200 exhibitors on one of the largest exhibition floors
in Europe
•  Unparalleled multi-disciplinary networking opportunities
•  Student and professional poster sessions
•  Active involvement of patient organisations
•  Pre-conference tutorials led by expert faculty
•  Hot topic sessions

To find out more about the EuroMeeting and to register your attendance, please click here.

Visit CK Clinical on Stand 714

So, if you are looking for a new position in the pharmaceutical industry, or are looking to expand your team, please come along to stand 714 to say hello. You could even be in with a chance of winning a Kindle by entering your business card into our prize draw!

Book an Appointment

Jonathan, Ben, Priya and Moin from CK Clinical are all available to book appointments with throughout the duration of the EuroMeeting. To find out more about them, please click on the links below which will direct you to their LinkedIn profiles. To book a meeting, please contact them directly on the details below. Thank you!

Posted in company news, NewsTagged in , , , , , , , , , , ,