Expert állások Svájcban (egészségügy, gyógyszeripar)

Collaborate closely with Translational Science Leads (TSL), Clinical Operations, Biostatistics/Bioinformatics, and Data Management teams to execute translational science strategies in clinical trials....

• Develop new product forms of fat-soluble and water-soluble actives, focusing on vitamins, carotenoids, and eubiotics to support animal health
• Formulation of product forms using emulsification, milling, spray drying, extrusion, and related formulation technologies

• Responsible of manufacturing planning & execution, industrial performance follow-up and reporting, crisis management and day-to-day management of our outsourced production by CMOs
• CMO Management in Mexico, Finland and Germany

• Active contribution to Product care and a Key role in Product development as the technical lead for the Orbit & Consumables portfolio
• Technical support of product development project team

• Lead and develop the Product Risk Management team
• Own and continuously improve the risk management process according to ISOwithin our product development framework
• Ensure high-quality risk analyses and maintain consistent, audit-ready risk management documentation

• Conduct HPLC analyses for release and stability testing of small molecules and professional use of various HPLC separation techniques.
• Work collaboratively on method validation and verification to support drug development program
• Data interpretation and exploitation in CDS

Commercial qualification with an advanced further education (e.g. Business Administrator) or a university degree in Business Administration...

• Responsible for project management of NIS and IIS
• Manage the publication processes related to clinical studies conducted by Octapharma
• Product reviews for submissions to international health-authorities
• Response to internal scientific questions
• Response to external medical enquiries

• Drive global CMC strategies for clinical trial applications, new product licenses, and post-approval changes.
• Assess CMC, facility/equipment, and plasma-related changes and manage regulatory submissions in coordination with regional teams.