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Associate Director of GCP Quality Assurance

£Competitive | East Midlands |  QA |  Permanent  | Ref:888370

Consultant

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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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The Role

Associate Director of GCP Quality Assurance - CRO - East Midlands - £Competitive

 

The Company

Our client is a highly passionate and innovative company providing CRO and CDMO global services including formulation development, clinical pharmacology trials, and clinical and commercial manufacturing services. Their growing business contains over 800 staff across the UK and USA who are instrumental to their success.

 

The Role

Due to successful business growth, our client is looking for an Associate QA Director with a background in a clinical environment and excellent leadership skills, to join their team in the East Midlands. Responsibilities of the role will include:

  • Provide QA oversight to assure clinical trial activities are conducted in compliance with GCP regulations and company procedures

  • Conduct internal, supplier audits and host client audits, providing leadership for GCP regulatory inspections

  • Contribute to strategic plans for the business in conjunction with Site Leadership Team members

  • Coach and develop staff, lead a team of 6 direct reports and encourage progression

  • Identify, communicate and escalate risks, serious non-compliance situations and root cause analysis

  • Review, approve and assure continued maintenance of Quality systems, change controls and CAPA's

 

You

  • Previous experience leading a Quality Assurance team in a CRO

  • Passionate about leading and developing team members and delivering excellent quality standards

  • Phase I or II experience is highly desirable

  • Experience and knowledge of GXP processes and regulations is essential

  • Change management and implementing systems experience in relation to Pharmaceutical, Clinical and Healthcare Industries

 

What should you do next?

This Director of QA role is one not to be missed; it encompasses the opportunity to develop a team in an innovative company. 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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