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We are currently looking for a Clinical Quality Systems (CQS) Manager to join our CMRS Quality Management Team at our operational HQ in Zurich. In this role you will be reporting directly to and be responsible for supporting the Head of Quality Management Clinical, Medical, Regulatory and Safety (CMRS). Your tasks and responsibilities will include, but not be limited to, the following:

• Daily operations of QM CMRS Training System (LMS), such as:


• 
  
  
  
  • User maintenance
  
  
  • Content management
  
  
  • LMS administrator support for Key Users and users
  
  
  • Annual reviews
  
  
  • Escalation of issues to LMS Support
  
  


• Daily operations of QM CMRS PD System (back-up), such as:


• 
  
  
  
  • Formatting and publishing of PDs
  
  
  • Support authors and approvers as needed
  
  
  • Quiz development/review
  
  
  • Workflow management
  
  


• Deliver QM CMRS departmental trainings as required


• Process improvement as applicable


• Support clinical/regulatory quality training and related systems 

The ideal candidate holds the following qualification and experience:

• Undergraduate degree in life sciences or equivalent


• 3-5 years’ experience in pharmaceutical industry / CRO with training system and document management experience


• Ability to independently manage processes within electronic quality management systems (SOPs, LMS, e-docs, SAP)


• Strong knowledge and understanding of GxP 


• Fluency in spoken and written English, any additional language is an advantage


• Proficiency in the use of relevant computer systems including complete Microsoft office suite (Visio and MS Project included)


• Experience with regulatory inspections and inspection readiness is preferred 


• Able to travel, as some travel may occasionally be required

You are self-motivated and bring strong inter-personal and communication skills (verbal and written), the ability to work independently and in a team environment. You have excellent organisational and management skills and are effective, efficient and timely in completion of duties. You have high ethical standards, integrity, and maintenance of confidentiality.

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

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