Required for Stability Specialist in Novartis
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post: Stability Specialist
Sound knowledge in pharmacopoeial compendia, good knowledge of current regulatory requirements, guidelines and cGMP.Quality experience (QA and QC) in a manufacturing environment within the pharmaceutical/ biopharmaceutical industry. Experience in manufacturing and working experience in SAP modules e.g., QM Quality Man-agement module, Material Management etc., Good know-how in common computer applications, i.e. MS Office, as well as in laboratory specific applications, e.g. GLIMS, Chromeleon, LIMS.
Ensuring regulatory compliance of all stability studies. Sound decision making on all aspects of stability. Communicates proactively (networking) with other departments in Locarno, external customers, e.g. manufacturing sites, TRD, GQO, SCM. Assumes responsibility and is a team player
Chemist or Pharmacist (BSc/MSc or B.Pharm/M.Pharm from accredited Technical University) or equivalent education with experience in pharmaceutical industry Local language, English fluent in speaking / writing At least 4 years Quality experience (QA and QC) in a manufacturing environment within the pharmaceutical industry. Experience in manufacturing desired.
Job ID: 172067BR
Business Unit: Global Develop NPH
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: R&D
End Date: 21st September, 2015
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