GMP QA Specialist — Investigations & Continuous Improvement

Baxter Healthcare; Zürich; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Baxter Healthcare in Switzerland is seeking a Quality Assurance Specialist to ensure plant activities meet GMP and Baxter quality policies. You will lead quality investigations, drive corrective actions, support supplier qualification, and help ensure regulatory alignment.

This role requires cross-functional collaboration, training, and continuous improvement across the site. Strong problem-solving skills and fluency in English and Italian are valued, with a engineering or scientific background

Qualifikationen

• Experience with Quality Management Systems in pharma/medical devices and GMP/ISO 13485.
• Degree in Engineering or Scientific field preferred, or equivalent experience.
• Proven experience managing investigations and corrective actions.
• Ability to operate in safety and internal quality procedures.
• Strong communication and collaboration across teams.
• Proactive approach with strong problem-solving capabilities.
• Good level of English and Italian.

Aufgaben

• Create, review, distribute and archive quality records per Good Documentation Practices.
• Lead non-conformity investigations and corrective actions.
• Drive supplier qualification and supplier quality activities.
• Support internal and external audits for compliance readiness.
• Provide training and coaching in quality areas.
• Review and update quality policies and the Quality Manual.
• Manage electronic quality documentation processes and ensure traceability.
• Collaborate with site departments to keep processes current and effective.
• Promote continuous improvement to enhance quality performance.

Kenntnisse

Quality management systems

GMP compliance

ISO 13485 familiarity

Cross-functional collaboration

Problem-solving

English and Italian language skills

Ausbildung

Engineering or Scientific degree

Jobbeschreibung

Baxter Healthcare in Switzerland is seeking a Quality Assurance Specialist to ensure plant activities meet GMP and Baxter quality policies. You will lead quality investigations, drive corrective actions, support supplier qualification, and help ensure regulatory alignment.

This role requires cross-functional collaboration, training, and continuous improvement across the site. Strong problem-solving skills and fluency in English and Italian are valued, with a engineering or scientific background