Regulatory Affairs Program Lead (Visp)

Lonza; Lavamünd; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career culture

Inclusive workplace

Compensation programs recognizing high

Benefits dependent on role and locale

Zusammenfassung

Lonza in Visp, Switzerland seeks a Manager Regulatory Affairs to lead end-to-end regulatory activities for complex client programs. You act as a regulatory advisor, aligning strategies, timelines, and deliverables with program objectives across global RA networks.

You will oversee submissions, lifecycle management, and health authority interactions, ensuring compliant, timely regulatory milestones and a strong link between regulatory requirements and project execution.

Qualifikationen

• Academic degree in Chemistry, Biochemistry, Pharmacy, or related science.
• Experience in pharmaceutical/chemical/biotech industry with GMP-regulated manufacturing.
• Strong cross-functional collaboration and translating requirements into execution.
• Experience with regulatory activities (submissions, lifecycle management) is a plus.

Aufgaben

• Lead end-to-end regulatory activities for assigned Visp client programs.
• Act as Regulatory Affairs Project Lead, aligning strategy, timelines and deliverables.
• Coordinate regulatory workstreams across internal functions and global RA networks.
• Drive prioritization, planning, and tracking of regulatory deliverables across programs.
• Ensure efficient day-to-day regulatory activities, including submissions and health authority interactions.

Kenntnisse

Regulatory leadership

Cross-functional collaboration

Project management

GMP knowledge

Health Authority interactions

CMC regulatory topics

Ausbildung

Science degree (Chemistry/Biochemistry/Pharmacy)

Jobbeschreibung

Lonza in Visp, Switzerland seeks a Manager Regulatory Affairs to lead end-to-end regulatory activities for complex client programs. You act as a regulatory advisor, aligning strategies, timelines, and deliverables with program objectives across global RA networks.

You will oversee submissions, lifecycle management, and health authority interactions, ensuring compliant, timely regulatory milestones and a strong link between regulatory requirements and project execution.