• An internationally operating, innovative Swiss pharmaceutical company, a leader in its field
• Flexible working hours and extensive training opportunities
• A motivated multicultural team and environment

• Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to the corresponding business partner (Line Unit) and other QA Units in area of responsibility
• Write, review, decide on approval and/or release of GMP-relevant deliverables in order to ensure compliance with cGMP internal quality standards.
• Perform project related activities, e.g. TRD products portfolio, operational processes, Quality Risk Assessments.
• Support Project management functions as a project team member.
• Provide Quality Oversight and 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.).

• Masters (5 years in pharma quality)
• Languages: Fluent German and English required (oral & written) for 1 role // English Fluent and German nice to have for the second open role.
• Good knowledge of cGMP, working knowledge in technical development, production and QA.
• Sound scientific, technical and regulatory knowledge.
• Strong organizational and decision-making skills.
• Strong and proven ability to analyze and evaluate cGMP compliance.

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