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In this position, you work for the Quality Management department and report to the Head of Quality systems. You act as the quality representative for the QA Training for the system and participate in the preparation and follow-up of the Health Authority inspections. In addition, you take the responsibility of the internal GMP audits. Your main tasks are the following:

• Contribute to the realization of QA trainings (newcomers/ periodic GMP / LMS line Manager / edms contributor / Trackwise / Change Control) including the preparation of attendance certificates, quiz, correction of quizzes, session recordings, access requests and follow-up and archiving


• Make the Update of LMS training plans after validation


• Contribute to updating the Training and Documentation processes


• Prepare of excel files for validation


• Act as responsible of change management system and process in place 


• Act as the key user of Trackwise for Geneva Site (Quality Modules)


• Act as a trainer and give support to Trackwise users 


• Ensure GMP compliance and performance of quality management systems


• Contribute into the consolidation of Local and Corporate Quality KPIs


• Act as internal GMP/GDP auditor


• Act as a QA expert cross functionally

For this challenging position, we are looking for a rigorous and solution-oriented person bringing the following profile: 

• University degree as Pharmacist, Biochemist, Chemist or similar


• Ideally 3 years’ experience in a quality assurance or quality compliance function within the pharmaceutical industry


• Strong knowledge of the GMP guidelines’ compliance (GXP.ICH,Ph,Eur,..)


• Experience with GxP Documentation Management and Trackwise


• Experience with people training on quality systems (an asset)


• Fluent in French and English both in oral and written conversation

You are a pragmatic person who likes to identify and solves problems from the roots. Responsible and methodical, you enjoy taking initiatives and demonstrate a rigorous approach to document and file management, with high attention to details. You have excellent organizational skills and prioritize according to needs. You are an open communicator with good interpersonal skills, who is able to build good working relationships with colleagues.

Über uns

Die Vifor Pharma Gruppe ist ein globales Spezialitäten-Pharmaunternehmen. Sie hat sich zum Ziel gesetzt, globale Marktführerin in den Bereichen Eisenmangel, Nephrologie und kardiorenale Therapien zu werden. Das Unternehmen ist der bevorzugte Partner für Pharmaprodukte und innovative, patientenorientierte Lösungen. Die Vifor Pharma Gruppe will Patienten mit schweren und chronischen Krankheiten auf der ganzen Welt dabei helfen, ein Leben in besserer Gesundheit zu führen. Das Unternehmen entwickelt, produziert und vermarktet pharmazeutische Produkte für eine optimale Patientenversorgung. Die Vifor Pharma Gruppe nimmt in allen ihren Kerngeschäften eine führende Position ein und besteht aus folgenden Unternehmen: Vifor Pharma, Vifor Fresenius Medical Care Renal Pharma (ein gemeinsam mit Fresenius Medical Care geführtes Unternehmen); und OM Pharma.

Die Vifor Pharma Gruppe hat ihren Hauptsitz in der Schweiz und ist an der Schweizer Börse (SIX Swiss Exchange, VIFN, ISIN: CH0364749348) kotiert.

Weitere Informationen finden Sie auf www.viforpharma.com/career

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