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Compliance Management System; CMS Specialist; m​/f​/d

Job in 4040, Basel, Kanton Basel-Landschaft, Switzerland
Listing for: Corden Pharma GmbH
Full Time position
Listed on 2026-06-24
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 50667 - 64486 CHF Yearly CHF 50667.00 64486.00 YEAR
Job Description & How to Apply Below
Position: Compliance Management System (CMS) Specialist (m/f/d) | 50–60%

Our People Vision:

We strive for excellence. We share our passion. Together, we make a difference in patients’ lives.

Compliance Management System (CMS) Specialist (m/f/d) | 50–60% 6 months contract
  • Basel
  • as soon as possible
Your Role

In this role, you support the continuous development and optimization of our global Compliance Management System (CMS), working closely with the Head of Global CMS and the global compliance leadership.

You contribute to strengthening compliance structures across the organization by combining analytical thinking, regulatory understanding, and hands‑on execution.

What makes this role impactful:

  • Direct involvement in global compliance topics and risk management
  • Exposure to corporate and local compliance structures
  • Strong focus on process improvement, prevention, and awareness
Strategic
  • Support the continuous improvement of the global legal compliance framework
  • Evaluate and monitor regulatory developments and their business impact
  • Identify risks and contribute to the development of mitigation strategies and internal controls
Operational
  • Support risk assessments, monitoring activities, and internal audits [
  • Maintain and develop policies, processes, and compliance tools
  • Provide data privacy support (e.g. GDPR) and collaborate with local and external stakeholders
  • Deliver and support compliance training and awareness initiatives
  • Work closely with interdisciplinary teams across the organization
  • Degree in Law, Economics, Finance or a related field
  • First experience in compliance, legal, or risk management within CDMO/pharma/biotech
  • Strong understanding of regulatory and compliance frameworks (e.g. GDPR)
  • Confident handling of electronic systems and data
  • Excellent communication and stakeholder management skills
  • Fluent in English, additional languages are a plus
  • Self-driven, structured, and solution-oriented mindset
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