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Qualified Person

£Competitive | Yorkshire & The Humber, South Yorkshire |  QA |  Permanent  | Ref:888674

The Role

Qualified Person - Pharma - South Yorkshire - £Competitive


The Company

This is an exciting time to join an expanding, highly successful global pharma in their offices in South Yorkshire. They offer excellent training and development opportunities as well as great career progression opportunities.

  • Excellent career progression opportunities

  • Great training and development

  • Exciting and innovative product / therapy range


The Role

Our client is looking for a highly capable and dynamic QP to join their site in South Yorkshire on a permanent basis. Responsibilities of the role include;

  • Products manufactured within the European Union, the Qualified Person must ensure that each batch has been manufactured and checked in compliance with the laws

  • Be responsible as their primary function for ensuring that each individual batch of medicinal product has been manufactured and checked in compliance with the laws

  • Be able to prove their continuous training regarding the product type, production processes, technical advances and changes to Good Manufacturing Practice

  • Shall consider conditions of storage and transport for batches and samples, if sent separately, of products manufactured in part or in whole at other manufacturing sites before certification of a batch

  • Gain and maintain both access to and a working knowledge of all records relating to production, testing, on-going stability and quality of Perrigo products

  • The required technical agreements are in place

  • The self-inspection programme is active and current

  • The appropriate arrangements for distribution and shipment are in place



To apply for this role, you must;

  • Must be eligible to act as a Qualified Person in accordance with European directives 2001/83/EC as amended and 2002/20/EC as amended and meet all the relevant qualification requirements stipulated therein

  • must understand the relationships between the Quality Assurance, Technical Operations, Supply Chain, Artwork and Regulatory departments & CMO's

  • Excellent working knowledge of GMP regulations and distribution practices


What should you do next?

This QP role is one not to be missed; it encompasses the opportunity to join a changing and growing company in pharma! To discuss further, please submit your current CV.

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.



Nadya Libecans

Which team do you work in? 

Drug Development

Which area do you specialise in?

Quality Control and Assurance

How do you keep up-to-date with the latest news in your sector?

I frequently read articles on changes and happenings in the industry, stay well connected on LinkedIn and regularly check in with relevant industry professionals.

What's your favourite film and why?

Honestly, I watch so many films it's difficult to pick just one, so for today I'm going to go with Mermaids because you can't go wrong with Cher!

If you could invent one thing what would it be?

Definitely would have to be heels that turn into flats so that I wouldn't have to carry two pairs of shoes everywhere anymore

What makes you #DistinctlyDifferent?

I believe knowledge is power and I strive to learn as much about people and the industry as possible to build lasting relationships and produce the best results for candidates and clients. 


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