Senior Fellow - Technical Developer (m/f/d)
Firmenname für PREMIUM-Mitglieder sichtbar
- Mai 2024
- nicht angegeben
- CH-Basel
- auf Anfrage
- 25.04.2024
- 759022/1-en
Projekt Insights
Projektbeschreibung
Ihre Aufgaben:
• Lead and drive formulation development and manufacturing activities for assigned projects, ensuring scientific and technological excellence focus on parenteral drug products
• Collaborate closely with cross-functional teams to align formulation project plans with control strategies, project timelines, and overall development strategies
• Communicate and exchange knowledge with Biopharmaceutics Experts and internal subject matter experts to incorporate critical factors for absorption and DP-performance into formulation development strategy
• Generate accurate and comprehensive scientific documentation, including development reports and manufacturing instructions, to support development trials, process transfers, and supply activities
• Ensure compliance with regulatory requirements and support inspections by contributing to filing dossiers, addressing DP-related questions, and representing project/product-related aspects during internal and health authority inspections
Ihre Qualifikationen:
• Advanced degree in scientific or relevant discipline (Masters or equivalent)
• Desirable: Ph.D. in scientific or relevant discipline or equivalent
• Well-founded experience in the development of sterile pharmaceutical formulations
• Strong knowledge of relevant GxP regulations and policies related with aseptic/sterile manufacturing
Ihre Vorteile:
• Renowned pharmaceutical company
• International environment
Projektdauer: 12 MM++
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
• Lead and drive formulation development and manufacturing activities for assigned projects, ensuring scientific and technological excellence focus on parenteral drug products
• Collaborate closely with cross-functional teams to align formulation project plans with control strategies, project timelines, and overall development strategies
• Communicate and exchange knowledge with Biopharmaceutics Experts and internal subject matter experts to incorporate critical factors for absorption and DP-performance into formulation development strategy
• Generate accurate and comprehensive scientific documentation, including development reports and manufacturing instructions, to support development trials, process transfers, and supply activities
• Ensure compliance with regulatory requirements and support inspections by contributing to filing dossiers, addressing DP-related questions, and representing project/product-related aspects during internal and health authority inspections
Ihre Qualifikationen:
• Advanced degree in scientific or relevant discipline (Masters or equivalent)
• Desirable: Ph.D. in scientific or relevant discipline or equivalent
• Well-founded experience in the development of sterile pharmaceutical formulations
• Strong knowledge of relevant GxP regulations and policies related with aseptic/sterile manufacturing
Ihre Vorteile:
• Renowned pharmaceutical company
• International environment
Projektdauer: 12 MM++
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
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