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Regulatory Affairs Auditor

£30k-£50k + bonus + benefits | Yorkshire & The Humber |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:886225

Consultant

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Katie Goulbourn

Which team do you work in?
I work within the Drug Development team.

Which area do you specialise in?
I specialise in recruiting Junior to Director level Regulatory Affairs & Quality Assurance professionals within Pharma, Healthcare, Medical Devices and Animal Health. 

How do you keep up-to-date with the issues in your sector?
Speaking daily with clients and candidates keeps me on top of the latest industry trends and news, combined with regularly visiting relevant websites and reading articles.

What's your favourite film and why?
I absolutely love a good rom-com, my favourite would have to be The Holiday.

If you could invent one thing what would it be?
Trackable GPS microchips for cats and dogs - how has this not been invented yet!?

More

The Role

Regulatory Affairs Auditor, £30-50k depending on experience plus bonus and an extensive list of benefits, Yorkshire

Following a site restructure, one of the world's leading pharma and healthcare companies have an exciting opportunity for an experienced Regulatory Affairs professional or QA Auditor to progress into an Auditing role developing the full global Regulatory function.

 

The Company

  • This is an exciting time to join an expanding, highly successful global pharmaceutical company based at their Yorkshire site.

  • Ongoing site refurbishment with state of the art equipment and facilities including staff shop, canteen, subsidised coffee shop and dry cleaners

  • Excellent career progression potential, rewarding high performance and looking for the Managers of the future

  • City location close to major transport links and with plenty of free onsite staff parking

  • Extensive list of employee benefits including annual bonus, 10% contributory pension, family healthcare plan, 25 days annual leave, childcare vouchers, share schemes, initiatives and discounted products.

 

The Role

This is something a little different to your usual Regulatory Affairs role, offering development and training for the right candidate. You will be responsible for:

  • Hosting internal and external audits of the international global regulatory function

  • Development of processes and implementation of continuous improvement

  • Liaising with colleagues from Associate to Senior Management level, working in partnership with the regulatory team to ensure effective processes and working

  • Updating of the QMS and CAPA management

  • This role does not require someone to work on regulatory submissions etc.

  • There is so much scope to develop this role in the future, including the opportunity to build a team around you or progress your career into other areas of the business

 

You

Personality and communication skills are key for this role! Although training and development are offered this is not a graduate role and therefore, as a minimum, candidates must be able to demonstrate:

  • A couple of years' experience in either:- a regulatory affairs position with knowledge of product regulations OR- compliance auditing, with experience maintaining QMS systems

  • Experience within healthcare, medical devices or pharmaceutical is essential

  • Excellent communication skills are a must, with the ability and confidence to advise senior Regulatory colleagues on process improvements

  • An agile, dynamic and ambitious attitude, with the desire to progress through the company

 

What should you do next?

This Regulatory Affairs opportunity won't be around for long! If you are unsure and need some advice, give me a ring, otherwise just click apply, upload your CV and send, it's really that easy!

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.



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