1 Compliance Stellen in Martigny gefunden

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• Compliance with and assurance of the quality requirements for raw materials in the GMP environment
• Responsible QA representative for raw material-specific aspects during the entire manufacturing process of a pharmaceutical product as part of an interdisciplinary team
• Responsible for reviewing and approving raw material-specific documents (QC plans, sampling instructions, bills of materials, etc.)
• Processing and supporting OOS investigations, deviations, CAPAs and change control processes
• Support for supplier qualification activities
• Subject matter expert in regulatory inspections and audits

• Bachelor of Science in the field of natural sciences (e.g. biology or chemistry)
• Professional experience in the GMP regulated environment of the pharmaceutical industry
• First professional experience in the field of quality (QA or QC) in the pharmaceutical industry
• Experience in dealing with stakeholders at various levels
• Initial experience with TrackWise, SAP, LIMS and DMS is desirable
• Fluent in German and English

If you are interested in this position, we look forward to receiving your application via the online application form.JETZT BEWERBEN
Visp, Fully on site for 1st month of assignment and then Hybrid possibility for 2 days a week
Luciana Sardo+41 58 307 24 41FILIALEManpower Life Sciences Competence CenterPicassoplatz 44052 Basel