Manager of Quality Assurance
Allied Clinical Management GmbH, Germany

• Strengthen development projects within Chemical amp; Analytical Development
• Maintain quality standards for IT and GMP-processes within Chemical amp; Analytical Development
• Oversee supplier qualifications of raw materials, intermediates and active pharmaceutical ingredients for external projects
• Measure and approve changes, deviations, validations and qualification documents
• Approve specifications and test procedures for raw materials, intermediates and packaging materials
• Review of Master Batch records and executed Batch records
• Support the preparation for authorities and customer inspection

Requirements

• PhD in Chemistry (preferred) or Pharmacy or Biochemistry
• At least 3 years of working experience in development functions or product supply
• Knowledge of chemical production, quality control, quality assurance and international drug laws
• Profound GMP understanding in the area of chemical and analytical development and production

• Expertise in the development of peptides and oligonucleotides projects
• German and English written and spoken fluency

Job Rewards and Benefits