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Quality Specialist - Documentation

Job description

Quality Specialist - Documentation

Work for one of the world’s largest pharmaceutical companies as part of their growing Cork site which focuses on the development of ground breaking drugs and treatments. Provide quality insight across the site and act as an SME for the documentation system and QC Labs.

Responsibilities:

  • Oversee, manage and improve the storage of the quality documentation for the QC Labs and the site's Quality management System
  • Complete documentation audits
  • Provide assistance with and ensure compliance to relevant regulatory requirements
  • Assist with NCRs
  • Assist with Regulatory audits

Requirements:

  • Qualification within Science or Engineering discipline and 1 years’ experience within a quality documentation environment
  • cGMP experience

 

 To apply for this position please contact James Porter at Sigmar Recruitment T: +353 91 455305 E:   jporter@sigmar.ie  

All applications will be treated with the strictest of confidence.  Sigmar will never forward your CV to a third party without prior consent

 

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