Regulatory Affairs Lead — Basel Relocation & Swissmedic

Sandoz

Risch-Rotkreuz

On-site

CHF 120,000 - 150,000

Full time

11 days ago

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Job summary

Sandoz is seeking a Regulatory Affairs Specialist to drive the Basel relocation from Rotkreuz to Basel. You will own the address-change across all Swiss-market artworks and manage Swissmedic submissions, in coordination with RA, QA, and Supply teams.

The role requires strong regulatory project leadership, experience with packaging changes, and a focus on timely, compliant delivery of all regulatory activities associated with the relocation.

Qualifications

  • Bachelor’s degree in biomedical, life or pharmaceutical sciences or equivalent with substantial regulatory experience.
  • 3+ years of regulatory affairs experience including lifecycle changes and cross‑functional implementation.
  • Fluent German and English; French/Italian desirable.

Responsibilities

  • Lead the regulatory address-change workstream for Basel relocation and manage Swissmedic submissions where applicable.
  • Oversee artwork updates, packaging texts, and product information across Swiss market.
  • Coordinate cross‑functional RA, QA, Supply and artwork teams to ensure timely delivery and risk mitigation.
  • Maintain consolidated project tracker and provide progress reports to stakeholders.
  • Ensure archiving of regulatory documentation and compliant handover to permanent RA team.

Skills

Regulatory Affairs
Project leadership
Cross-functional collaboration
German language
English language

Education

Bachelor’s degree in biomedical, life or pharmaceutical sciences
Postgraduate qualification desirable

Tools

Excel
SAP
Regulatory databases
Artwork management systems

Job description

Sandoz is seeking a Regulatory Affairs Specialist to drive the Basel relocation from Rotkreuz to Basel. You will own the address-change across all Swiss-market artworks and manage Swissmedic submissions, in coordination with RA, QA, and Supply teams.

The role requires strong regulatory project leadership, experience with packaging changes, and a focus on timely, compliant delivery of all regulatory activities associated with the relocation.

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