QA Documentation Controller

Working in close partnership with an international advanced pharmaceutical and medical device business that are investing seriously into expanding their quality and operational activities, I am supporting the leadership team further build out the QA functions across multiple sites within the United Kingdom.
These brand new positions will take full day to day management of all things related to quality assurance documentation. This will include managing files, creating new technical documentation, overseeing SOP paperwork and administering the training system files.
Due to the size of the team and sites, the role will be broad and varied and you will have a chance to work directly with various departments, further building your exposure in a pharmaceutical setting.
This is a fantastic opportunity for an experienced QA professional to further develop their career with a systems pathway, or even someone that is looking to break into a QA role (perhaps from QC or production settings). Either way, this business can bring you in and support you at the right level.
There Are Positions Across The Following Regions

• London
• Surrey
• Lancashire
• Staffordshire
• South Yorkshire
  

Key Experience

• Experience and/or understanding or quality assurance documentation
• Understanding of GMP – although you may have worked with other compliance systems
• Transferable experience to demonstrate accuracy and the ability to work in an administrative capacity with highly regulated documentation
• Flexible and adaptable in your approach to work
• Strong communication skills with the capability to work in a small team
  

Please apply below or contact Mark Bux-Ryan for further information.
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