Stellen-ID: 60601
Standort:Springe, DE Stockholm, SE Lingolsheim, FR Wien, AT
Karrierestufe: Experte
Fachbereich: Quality
Beschäftigungstyp: Festanstellung
Karrierestufe:
Octapharma is a global company whose products support patients in 118 countries worldwide. Our medicines are high-quality human proteins extracted from human plasma and human cell lines.
Octapharma Produktionsgesellschaft Deutschland mbH (OPGD) in Springe near Hanover is one of five state-of-the-art production sites. There, our approximately 800 employees manufacture the finished medicinal product albunorm® as well as intermediate products for further processing.
We look forward to continuing our growth together with you (m/f/d) as Group Analytical Specialist QC (m/f/d) - Method Validation starting immediately.

• Prepare validation documents and other GMP-relevant documents with the support of senior analyticalspecialists and team leaders
• Develop and validate methods
• Support troubleshooting in the QC laboratories
• Manage sample administration and follow-up of validation-related testing in the QC and R&D laboratories
• Support method transfer and the issue/update of product specifications
• Administer documents required for submission and assist with inspection tasks
• Prepare statistical evaluations of data and reports using Excel