We are seeking support in operational quality management for a leading international biopharmaceutical company as  a specialist in the quality department. 

Your tasks:

• Review and approval of packaging specifications
• Maintenance and release of master data, data records and bills of materials
• Quality Oversight in SAP, MDG, MES or similar systems
• Review and approval of change controls and document changes
• Ensuring compliance with SOP and GMP requirements
• Data maintenance and creation of quality-relevant analyses and reports
• Support and advice on GMP and compliance issues
• Creation and coordination of risk assessments
• Participation in quality-related and cross-departmental projects

Your profile:

• Experience in the quality environment of a regulated company
• Good knowledge of SAP, MDG, MES or comparable system landscapes
• Understanding of GMP, Change Control and Document Management
• Structured, precise and pragmatic working method
• High attention to detail combined with efficient work practices
• Good prioritization skills in a dynamic work environment
• Strong communication skills and enjoyment of cross-functional collaboration
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