Quality Specialist - Heparin manufacturing, LEO Pharma, Esbjerg, LEO PharmaAnnoncencen er hentet fra: Jobindex
Quality Specialist - Heparin manufacturing, LEO Pharma, Esbjerg
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:
Indrykket 13. september
- 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)
Denne annonce er opslået d. 13-09-2017 og må derfor antages for at være udløbet.
Annoncen er medtaget fra vores arkiv og kan kun anvendes som reference.
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