Senior Quality Manager (m/f/d)

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

• Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility
• Write, review, decide on approval and/or release of GMP-relevant deliverables and/or related tools as per area of responsibility in order to ensure compliance with cGMP and project quality deliverables
• Manage project related activities e.g. TRD product portfolio, development of new tools, processes, Quality initiatives, Quality Manual implementation, Quality Plans, Quality Risk Assessments, training activities, qualification and facility upgrade activities, IT validation projects as per area of responsibility
• Support Project management functions as a project team member
• Provide support to TRD line functions in GMP related topics as per area of responsibility
• Comply with internal and external guidelines regarding quality and safety, Quality Manual, regulatory cGMP guidelines, Health Authority guidance, SOPs etc.
• Approval of Deviation
• Approval of Change Controls
• Approval in document management system SUBWAY of technical file (DHF) documents
• Support Audits and self-inspections within TRD and clinical space

• University Degree in a relevant field
• Experience in pharma quality or operations
• Profound English knowledge
• Profound German skills
• Profound knowledge of cGMP, working knowledge in technical development, production or QA
• Sound scientific, technical and regulatory knowledge
• Organizational and decision-making skills
• Ability to analyze and evaluate cGMP compliance
  

• Renowned pharmaceutical company
• International evironment
• Possibility for home office

Ihr Kontakt

Referenznummer
786900/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

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