QC Associate Scientist (m/w/d)

Your tasks:

• Conducting laboratory investigations, critical material qualification, and method transfers
• Authoring transfer protocols and reports, developing qualification plans for critical reagents
• Overseeing validation and qualification activities, providing training and support as needed
• Investigating and troubleshooting problems, conducting risk assessments and root cause analysis
• Owning laboratory investigations and CAPA processes
• Supporting daily QC activities, ensuring compliance with cGMP, internal policies, and EHS requirements

Your experience/knowledge:

• 1+ years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment
• Background in GMP Laboratory activities with hands-on experience with statistical tools
• Solid knowledge of method transfer and critical reagent qualification
• Proficiency in all aspects of standard IT tools
• University or engineering degree in analytical chemistry, biotechnology, biochemistry