Manufacturing Specialist

Job Title: GMP (Solid Oral Dosage) Production Specialist (m/f/d)

6 months, Full time, remote, B2B

Responsibilities

• Manage and technically process deviations, including root cause analysis, and define/track CAPAs
• Provide project-based support for CAPA and complaint management
• Create, review, and optimize SOPs and GMP documentation
• Conduct risk assessments (e.g., FMEA) and provide technical action recommendations
• Develop, prepare, and deliver GMP training as an external training service
• Perform technical reviews of manufacturing and testing documentation
• Advise department management on defined GMP and process optimization projects

Requirements

• Degree in a scientific discipline or comparable qualification
• ≥5 years’ experience in a GMP-regulated environment
• ≥3 years’ experience in solid dosage manufacturing
• Strong knowledge of deviation/CAPA management and EU-GMP regulations
• Structured, independent, and solution-oriented working style