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. This is an exciting opportunity for individuals passionate about quality assurance in the pharmaceutical industry.

Please note that 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.
• Activel...