Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. By creating a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally. Join us, the future is ours to shape!
This position is a strategic role for Sandoz Regulatory Affairs to drive compliance topics, process and efficiency topics, audits, inspections and risk management tasks under one umbrella of Regulatory Operational Excellence within Sandoz Regulatory Affairs. It includes the audit/inspection management in Regulatory Affairs, as well as compliance topics , including the quality management oversight with the corresponding quality key indicators such as metrics, deviations, escalations, trainings, etc. Keeping the strategic oversight, negotiation and influencing skills as well as problem solving are key elements for this role.

YOUR KEY RESPONSIBILITIES:

Your responsibilities include, but not limited to:

WHAT YOU’LL BRING TO THE ROLE:

• University Degree, preferable Master in Bio-Medical / Life Sciences / Pharmaceutical sciences.
• Extensive experience in the pharmaceutical industry + Regulatory Affairs (> 5 years)
• Strategic leadership skills
• Strong influencer, negotiator, and collaborator in a matrix environment beyond function / area of expertise
• Understanding and experience of quality and compliance
• Understanding and experience with process optimization
• Stakeholder management
• Project Management skills
• High change ability
• Ability to manage operational and strategic workload
• Prioritization and decision taking
• Communication skills for complex topics
• Result oriented
• High ethical standards
• Fluent in English (written and oral), German is an advantage