GMP Compliance and Deviation Management Specialist | Mitarbeiter GMP Compliance / Abweichungsbearbeitung (m,w,d)

Proclinical GmbH

Marburg, Hessen, Deutschland
Published Dec 12, 2025
Full-time
Fixed-term

Job Summary

This role involves supporting a pharmaceutical client in Marburg, Germany, focusing heavily on maintaining GMP compliance and managing complex deviations. The specialist will be responsible for the initial assessment, coordination, and processing of complex deviations, as well as developing, implementing, and coordinating Corrective and Preventive Actions (CAPAs) to prevent recurrence. Key tasks include conducting complex risk analyses, creating change controls in both German and English, and actively supporting national and international regulatory and customer inspections, including presenting deviation reports and addressing deficiencies in both languages. The ideal candidate holds a degree in a natural science field, possesses strong German and English language skills, and has initial experience in deviation handling within a GMP-regulated environment. This is an excellent opportunity to gain long-term experience in the stable pharmaceutical industry, with potential for permanent employment.

Required Skills

Education

University degree in Natural Sciences (e.g., Biology, Chemistry, Pharmacy)

Experience

  • Initial experience in deviation processing within a GMP-regulated environment
  • Professional experience in conducting risk analyses
  • Experience in leading local and global project teams

Languages

German (Fluent)English (Fluent)

Additional

  • Temporary contract (Befristet)