Beschreibung

In this role, you will oversee critical project tasks while authoring essential documentation. Your work will involve managing stability studies and validations, ensuring compliance, and supporting the lab team in resolving complex issues.

Anforderungen

• •Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry or similar
• •At least 4 years strong relevant industry experience or PhD in relevant field or equivalent
• •2+ years of work experience within the pharmaceutical industry
• •Proficiency in English and German
• •Good knowledge of sound technical & scientific of pharmaceutical, chemical analytics, QC or equivalent
• •Proven experience within GMP environment
• •Good theoretical and scientific knowledge in the area of expertise (like HPLC, CE)
• •Can-do mindset and adaptability to change
• •Strong communication across organizational interfaces and presentation skills
• •Ability to work and lead a cross-functional team in a matrix

Aufgaben

• •Manage key project tasks independently
• •Write protocols and scientific reports
• •Prepare ready-to-submit documents for submissions
• •Approve GMP documents and test records
• •Investigate quality events within projects
• •Support the lab team in troubleshooting methods and processes

Tools & Technologien

Benefits