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Qualified Person

£Negotiable DoE | South East |  QA |  Permanent  | Ref:887761

Consultant

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Hayley Shayestehroo

Which team do you work in?

I work in the Regulatory Affairs team.

Which area do you specialise in?

I specialise in recruiting all levels of Regulatory Affairs professionals within pharma, healthcare and medical devices. 

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

Speaking to candidates is the best way to keep updated with changes in the market. I also like to read relevant industry press and relevant articles on LinkedIn. 

What's your favourite film and why?

Mrs Doubtfire - it's an all time classic and I pretty much know it word for word. I love a good thriller too, anything with a good twist at the end. Law Abiding Citizen with Gerard Butler is one of my faves. 

If you could invent one thing what would it be?

Pizza that makes you slim! 

What makes you #DistinctlyDifferent?

I love watching pretty much any sport. I play netball twice a week and come from a footballing family, so have been taught how to do kick ups (my record is 21 without hitting the floor!) Work wise, I like to think I get to know candidates on a deeper level and really understand their drivers and motivations for moving to another company. 

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The Role

Qualified Person, Leading Research Organisation, Reading £Negotiable DoE

 

The Company

This is a fantastic opportunity to join an international leader in the world of Clinical Research. My client is unique in their ability to offer a complete range of services centred around production, implementation and development of innovative treatments and products for the healthcare industry. They are extremely passionate about their employees and pride themselves on a supportive and friendly environment with the highest standards of training:

  • Provides comprehensive support and regular training

  • Friendly, welcoming and supportive environment

  • Varied environment; no two days are the same

 

The Role

As the Qualified Person you will be responsible for;

  • Responsible for batch reviews, certification and release of manufactured, assembled or important IMPs (Investigation medicinal products)

  • Oversee the Product Specification File for each study

  • Review and approval of master batch records, development protocols and out of spec results, lab investigations

  • Assist with all aspects of GMP audits

 

You

As the Qualified Person you will have the following experience:

  • Qualified to act as a QP for Investigational Medicinal Products (IMPs)

  • Worked on large scale batch releases

  • Experience with solid dosage forms (capsules and tablet formulations), inhalation products and non-sterile liquids would be advantageous

 

What should you do next?

This Qualified Person 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.



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