Quality Specialist - Heparin manufacturing, LEO Pharma, Esbjerg, LEO Pharma

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LEO Pharma
Quality Specialist - Heparin manufacturing, LEO Pharma, Esbjerg

LEO Pharma

The department consists of nine people with responsibility for the full range of cGMP compliance activities – release of raw materials, intermediates and the final API, validations and qualifications, hosting inspections, quality management systems and providing daily compliance support to the manufacturing teams. Two of these quality positions are located in Esbjerg – the rest are in Cork.

ou will support the first manufacturing steps of the Heparin supply chain in Esbjerg including the supply of mucosa from abattoirs. Your primary responsibilities will be:

  • release of mucosa and raw materials (Batch record and QC data review)
  • daily compliance support to manufacturing (Deviation and Change Control handling, SOP approval, approval of validation and qualification documents)
  • activities related to the abattoirs (participation in scheduled visits)
LEO Pharma

Indrykket 13. september

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Denne annonce er opslået d. 13-09-2017 og må derfor antages for at være udløbet.
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