QA Validation Specialist- New State of the Art Facility

QA Validation Specialist - Fastest growing Biopharma Company

This is a great role for a professional to be involved in a QA position for a global leading organisation. Working closely with your line manager, your role will be focused on validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures

My client, one of the faster growing biopharma companies globally, is now looking for a QA Validation Specialist to help with the fast developing of the company.

If you have a minimum 3 years of experience in QA validation within the Pharma Industry working in a manufacturing site with biologics, then this is the right opportunity for you.

In return, you will get to be part of company which managed to build a new site and grow it to over 700 employees in less than 4 years and they are not showing sings of stopping anytime soon. You will be part of the largest biotech manufacturing site in Europe and you will have the chance of developing and growing at the same fast pace as the company putting you on a fast track professionally.

Due to the fact that this is a new site, you will also be working with cutting edge equipment in a state of the art facility making you

Main duties include:

* Generates, executes and/or reviews master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria
* Reviews, edits and approves deviation notifications, deviation investigations, and corrective actions.
* Reviews, edits and approves change controls, SOPs, reports and other documentation
* Manages projects and prepares status reports
* Reviews, edits and approves deviation notifications, deviation investigations, and corrective actions.
* Investigates and troubleshoots problems which occur and determines solutions or recommendations for changes and/or improvements
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This is an English speaking environment and experience in UK or the EU is needed.

For a confidential discussion about quality assurance, then send your CV in Word format (I am unable to accept PDF's) to E.Cazacu@nonstop-recruitment.com or call me, Elena Cazacu, Quality Assurance Consultant for UK and Ireland on +44 207 940 2105.
NonStop Pharma is Nonstop Recruitment's longest running division with an ever growing number of consultants covering a wide range of niche specialisms across Europe. Owing to our breadth and depth of coverage we are well equipped to provide specialist support to a full range of services from large scale recruitment campaigns to executive searches and permanent to interim positions. For more information, see our website, http://www.nonstop-recruitment.com/ .
Also if you believe that these might not be the right opportunities for you but you know someone else who is looking for this kind of positions please feel free to refer them to us and you could gain £200 in high street vouchers if we successfully manage to place them.
Please note we can only accept applications from candidates who hold valid European Union passport and are able to work in Europe without visa sponsorship.
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