Are you experienced in digitalizing the manufacturing processes of pharmaceutical products? We are looking for you!
More information available upon request.
– Deploying, maintaining and implementing changes in computerized systems.
– Contribute in digitalization of manufacturing processes
– Training, support and improvement projects around systems (MES, LIMS, ERP etc.)
– Act as MES EBR editor and MES Key User
– 5+ year expereince as process engineer/MES specialist in GMP setting
– Exellent knowledge of pharmaceutical manufacturing processes
– Experience with writing and execution of CSV documentation/protocols
– Ability to take the lead and drive projects and changes
– Be able to work on-Call / On stand-by outside office hours
The employment conditions are up to market standard.
+316 2125 4820
Please send your application through our website.