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Regulatory Compliance Senior Associate Cross Category

£Negotiable DoE | Yorkshire & The Humber |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889060

The Role

Regulatory Compliance Senior Associate Cross Category - Global Healthcare Company -Yorkshire - £Negotiable DoE

 

The Company

This is an exciting time to join an expanding, highly successful global healthcare company based either at their Yorkshire site. Fantastic refurbished offices with many facilities including staff shop, canteen, subsidised coffee shop and dry cleaners.

  • Excellent career progression opportunities

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

  • Great benefits with bonus, pension, healthcare, share scheme and discounted products

 

The Role

As the Regulatory Compliance Senior Associate Cross Category, you will be responsible for;

  • Responsible for post approval maintenance activities for a range of products cross category. These can include, medicines, cosmetics, chemicals, biocides and medical devices

  • Developing global regulatory strategies

  • Project management of post approval activities (safety variations, monitoring, updating regulatory documentation)

 

You

You will have the following experience:

  • Hands on regulatory affairs experience, ideally in post approval maintenance

  • Experience in any of the following; Medicinal, Cosmetics, Chemicals or Medical Device Regulatory Affairs

  • Experienced setting global regulatory strategies

 

What should you do next?

This Regulatory Compliance Senior Associate Cross Category job is a great role and won't be around for long! So don't delay. 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.

Consultant

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Hayley Shayestehroo

Which team and area do you work/specialise in?

I work in the Regulatory Affairs team and recruit for Regulatory Affairs professionals at all levels within Pharma, Medical Devices companies and Regulatory Consultancies

 

What are some of the typical roles you cover?

I cover Regulatory Affairs positions at all levels within Pharma, Medical Devices and Regulatory Consultancies, these typically include;

Regulatory Affairs Associate jobs, Regulatory Affairs Executive jobs, Regulatory Affairs Senior Associate jobs, Regulatory Affairs Manager jobs, Regulatory Affairs Senior Manager jobs, Regulatory Affairs Director jobs, Regulatory Affairs Consultant jobs, Regulatory Writer jobs and Medical Writer jobs.

 

What are the hot issues in your sector currently?

Within Medical Devices it is the transition from MDD to MDR in May 2020. A lot of medical device companies are hiring Regulatory professionals to prepare their company for the transition

 

What is your greatest fear?

I don’t really have one, but if there’s one thing I’m well not keen for it would be snakes or an army of ants…

 

How would your friends describe you in three words?

Funny, healthy, sporty

 

You’re stranded on a desert island – what one thing could you not live without?

Bear Grylls! He’d have us rescued in no time!

 

What’s makes you #DistinctlyDifferent?

I take pride in getting to know my candidates on a personal level as well as professional. Changing jobs is a big decision for most people so I like to ensure I am placing my candidates in a role that not only matches their career aspirations but also suits their personal situation and key motivations.

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