By optimizing analytical and quality control processes, you will enhance the efficiency and effectiveness of our clinical and commercial production pipelines, securing the high standards of pharmaceutical manufacturing.
Regulatory & Compliance Excellence: Ensure robust data integrity practices and compliance with global regulatory standards (cGMP, ICH, FDA, EMA). Degree in natural sciences, pharmacy, engineering, or a related field. Proven experience in effectively managing CMC-QC portfolios of multiple late-stage clinical products including incoming goods, finished product and stability studies & expertise in quality management systems, with a focus on method validation, data integrity, and compliance.
Regulatory Know-How: In-depth knowledge and hands-on experience of regulatory requirements for clinical and commercial production, including experience with FDA and EMA inspections.
Your Benefits:
Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning
Job ticket | Deutschlandticket
Apply to our Marburg, Germany location by sending us your documents via our online form.