Junior Docs Specialist - Digital Records & Compliance

CK QLS; Luzern; Hybrid; CHF 90.000 - 115.000; Vollzeit

Zusammenfassung

CK QLS seeks a documentation-focused professional to join the Pharmaceutical Analysis & Digital Technologies (PADT) group for a 6-month program. You will support Metrology & Validation and Compliance, developing and maintaining a robust digital documentation system to ensure ALCOA+ compliant records and quick access.

The role emphasizes GMP-aware documentation control, cross-functional collaboration, and on-site work with occasional approval for home office as needed in coordination with

Qualifikationen

• Apprenticeship or university degree in biotech, pharma, QA or regulatory compliance.
• Strong English (B1) and German (B2) communication.
• Experience with GMP environments and documentation control.

Aufgaben

• Manage day-to-day documentation storage and archival for Metrology & Validation and Compliance teams.
• Develop a digital documentation management process ensuring quick access to documents.
• Archive documents per record retention policies and ensure traceability.
• Coordinate with cross-functional teams to ensure compliance of documentation management.

Kenntnisse

English (B1)

German (B2)

Ausbildung

Apprenticeship or university degree in Biotech/Pharma/QA or Regulatory Compliance

Tools

GMP documentation tools

Project management tools

Jobbeschreibung

CK QLS seeks a documentation-focused professional to join the Pharmaceutical Analysis & Digital Technologies (PADT) group for a 6-month program. You will support Metrology & Validation and Compliance, developing and maintaining a robust digital documentation system to ensure ALCOA+ compliant records and quick access.

The role emphasizes GMP-aware documentation control, cross-functional collaboration, and on-site work with occasional approval for home office as needed in coordination with