Drive pharmaceutical innovation as the Manager of Analytical and Manufacturing Activities. Oversee technical processes and compliance in collaboration with external manufacturing organizations for clinical programs.
Your role will focus on managing GMP processes for drug substances. You will also be responsible for supporting analytical development and validation activities while reviewing documentation to maintain cGMP compliance. Additionally, you will provide expertise in new product formulations and process development.
Key Responsibilities:
• Manage external analyses and manufacturing operations
• Lead GMP production for nasal drug formulations
• Ensure compliance through thorough documentation reviews
• Support stability programs and data trending
• Guide technical recommendations to Quality Assurance
Requirements:
• BSc or MSc in a relevant scientific field
• Over 5 years of experience in biotech or pharmaceuticals
• Hands-on experience in GMP an...