The role
As lead auditor you will perform and document GMP compliance audits in accordance with internal requirements as well as participating in the continuous improvement of quality metrics. You will also follow up on regulatory trends and participate in compiling input on GMP related regulations and guidelines. Further to this you will support the sites in preparing and managing health authority inspections and customer audits. As well as this, you will participate in developing and maintaining a global platform for sharing of Regulatory Inspection Deficiencies as well as significant customer audit observations to ensure such information is communicated, tracked and responded to accordingly by all GMP sites.
The Qualifications
  • BSc or MSc in biochemistry/biology, chemistry, pharmacy or equivalent
  • 5+ years of experience as a GMP auditor
  • Quality Assurance / Quality Systems experience in a cGMP environment (10+ years)
  • Experience in biological and/or chemical API Quality assurance as well as regulatory inspections
  • Strong communication and interpersonal skills. Organizational skills in multicultural environment
  • Excellent knowledge of the English language plus preferably other languages
In short, for the moment, that is all that you will need to know. If you are interested, then contact me immediately bmorina@barringtonjames.com with a copy of your cv and/or contact details to save yourself missing out on this great company and their huge future plans.
Someone to spring to mind? If you have had the pleasure of working alongside some of the best GMP auditors in the industry and feel they deserve to be a part of this amazing new developments, send me their names and number and I will let them know that you recommended them…unless of course you would rather I kept that information confidential…and I will also reward you with £/€500 for referring them to their dream job.Apply now