Polpharma Biologics requires a mid to
Requirements:
Stability studies for proteins (macromolecules),
Peptide mapping analytical method
Analytics of Biopharmaceuticals (Proteins) in a QC environment
Practical and theoretical knowledge in chromatography, electrophoreses, pH, subvisible particle measurement performed in a QC environment
Designing, managing and performing of stability studies of Biopharmaceuticals
Knowledge in all topics needed for Biopharmaceuticals like Setting specification, establishment of reference standards
Experienced in all GMP topics like handling OOS, Deviations, change requests
Length of contract – 6 months
Availability – 4 – 5 days onsite per week.
Compétence attendue : Expérience sur les macromolécules et gestion d’études de stabilité
2019-07-Polpharma-hiring