GMP Documentation & Compliance Specialist (Temp)

Michael Page; St. Niklausen; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Benefits dieser Stelle

Compliance project

Lab operations exposure

International environment

Career development

Hands-on role

Zusammenfassung

Michael Page in Switzerland is seeking a Documentation & Compliance Coordinator to support GMP-regulated operations. You will manage the documentation lifecycle, coordinate control activities across lab equipment, validation, and training records, and help implement digital document management solutions.

The role requires a life sciences or QA background, strong attention to detail, and experience with regulated documentation.

Qualifikationen

• Experience managing technical, quality, or regulated documentation.
• Strong attention to detail and accuracy with large document volumes.
• Familiarity with GMP-regulated environments is advantageous.
• Exposure to audits or regulatory inspections is a plus.

Aufgaben

• Manage and maintain documentation lifecycle from creation to archival.
• Coordinate document control activities supporting lab equipment, validation, training records, and compliance.
• Contribute to digital document management solutions implementation.
• Ensure records are retained and retrievable per procedures and regulatory requirements.
• Collaborate with Quality, Validation, Compliance and technical teams to maintain inspection readiness.
• Support audits, inspections, and internal reviews with document-related expertise.

Kenntnisse

Document control

Quality assurance

Regulatory affairs

English and German communication

Ausbildung

Bachelor's degree or apprenticeship in Life Sciences or related

Tools

Document management systems

Jobbeschreibung

Michael Page in Switzerland is seeking a Documentation & Compliance Coordinator to support GMP-regulated operations. You will manage the documentation lifecycle, coordinate control activities across lab equipment, validation, and training records, and help implement digital document management solutions.

The role requires a life sciences or QA background, strong attention to detail, and experience with regulated documentation.