Beschreibung

In this role, you will transform complex biopharmaceutical data into clear, structured documentation, ensuring compliance and transparency throughout the development and manufacturing processes. Your responsibilities include analyzing data, drafting reports, and maintaining high quality standards.

Anforderungen

• •Degree in a scientific discipline
• •Peer-reviewed publications as first author
• •Knowledge of biotechnological development processes (USP/DSP)
• •Excellent English skills (written and spoken)
• •Solid understanding of DoE and biostatistics
• •Basic project management knowledge
• •Ability to present complex data clearly and logically
• •Strong attention to detail in language, scientific accuracy, and formatting
• •Proficiency in MS Office and JMP
• •Experience in preparing regulatory documents is advantageous
• •Skills in visualizing scientific content is a plus
• •Affinity for interdisciplinary collaboration

Aufgaben

• •Analyze raw data from process development
• •Prepare and review reports from Process Science and Manufacturing Science and Technology
• •Draft and review protocols, policies, and overarching SOPs
• •Write clear, structured reports for early, late-stage, and commercial process development
• •Present complex data in an understandable and scientifically accurate way for stakeholders
• •Ensure high standards in grammar, scientific precision, layout, and design
• •Contribute to document harmonization and standardization projects

Tools & Technologien

Benefits