Ensure cGMP excellence by safeguarding analytical compliance in a world‑class Swiss quality organization.

Proclinical is seeking an Analytical Compliance Record Specialist to join a quality‑focused team in Switzerland. This role involves working within a modern quality control organization to ensure compliance with cGMP regulations. You will play a key role in managing compliance records, facilitating root‑cause analyses, and supporting inspections.

Note: To be considered for this role, you must have the right to work in this location or hold an EU passport.

Responsibilities

• Manage compliance records for the department, including deviations, changes, and CAPAs.
• Collaborate with stakeholders such as QA, scientists, and senior management.
• Facilitate and document root‑cause analyses.
• Actively participate in quality review boards and other strategic governing bodies.
• Support inspections by preparing and p...