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Regulatory Affairs Technical Manager

£competitive | London |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:886154

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 Technical Manager, £competitive plus bonus, Central London

Excellent opportunity for a highly experienced Regulatory Manager to work autonomously in a relatively small yet established company.

 

The Company

  • Based in one of the most desirable locations in Central London!

  • Manufacture, market and supply generic pharmaceutical products

  • European company, with a relatively new UK office supplying specifically into the UK market

  • Modern offices surrounded by coffee shops, lavish restaurants and designer shops

  • City centre location, across the road from the tube station

  • List of employee benefits include annual bonus, private family healthcare, 6% contributory pension, life insurance at 4x salary, 25 days annual leave

 

The Role

The Regulatory Affairs Technical Manager will be responsible for a wide remit including:

  • Preparation of submission and licence dossiers, including UK eCTD

  • Ensuring regulatory and GMP compliance

  • Developing and executing of regulatory strategy

  • Supporting the QP on related duties including audits, SOPs, change controls, deviations, CAPAs etc.

  • Liaising with external PV provider including PSUR's, SDEA's and RMP's

 

You

To be considered you will be able to demonstrate:

  • A minimum of 5 years varied Regulatory experience is essential

  • Generics pharma experience within the UK market is essential

  • Some knowledge of quality processes, including SOPs, change controls, deviations, CAPAs

  • Experience to hit the ground running with minimal to no supervision

  • Experience driving projects through to conclusion including communicating with various stakeholders

 

What should you do next?

This Regulatory Affairs Manager 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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