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Quality Manager ISO 17025

£Competitive + benefits | North West, Greater Manchester |  QA |  Permanent  | Ref:887907



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. 


The Role

Quality Manager ISO 17025 - Lab Analytical Services - Manchester (flexible) - £Competitive + benefits


The Company

Our client provides drug discovery, development and analytical services specialising in the pharmaceutical, biotech, environmental, food and chemical sectors

  • Ranked within the top 20 fastest growing UK pharma companies by Alantra in May 2018

  • 10 locations across the UK each with on-site laboratories

  • Learning and development opportunities along with a structured career progression scheme


The Role

Our client has an exciting opportunity for a highly experienced Quality Manager ISO 17025/ GMP

  • You will lead the existing QA teams across the company's UK sites to provide compliance oversight on GMP and ISO regulations

  • Host Accreditation and Regulatory Inspections along with developing the auditing strategies to ensure the company meets the requirements of the regulations

  • Other responsibilities include engaging all QA employees with objectives to ensure consistency across the business, implementing the QMS and existing systems and monitoring the development and performance of QA team



To apply for this role as a Quality Manager ISO 17025/GMP, our client is looking for a highly skilled candidate with experience of managing ISO 17025/GMP standards, guidance and regulations

  • It is essential to have strong managerial skills and the ability to lead multiple teams

  • You must have experience in influencing, impacting and leading QA operations through developing audit schedules and training initiatives

  • Travel within the UK is required on a regular basis, so a driving license is highly desirable


What should you do next?

This Quality Manager role is one not to be missed; it encompasses the opportunity to progress in an exciting and growing organisation. 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.

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