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Merck KGaA·1 day ago
1 day agoBe an early applicant

Regulatory Affairs Manager (all genders)

Zug, SwitzerlandFull-timeSenior · 5-10 yearsRegulatory Affairs Specialist

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Top 10%Top 10%: 19 out of 100

Top 10% of NextRaise users, across all roles in this function in Switzerland.

Must-have skills for this role

  • regulatory affairs
  • regulatory compliance
  • marketing authorization submission
  • life cycle management

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What you'll do

  • Support our local Regulatory Team in Zug
  • Oversee the submission strategy for new medicinal products
  • Manage the lifecycle of existing ones
  • Ensure compliance with local regulations

What they're looking for

  • Significant regulatory experience in Switzerland
  • Pharmacy, medicine, or natural sciences degree
  • Strong analytical and communication skills

Summarised by NextRaise from the employer’s description, which follows in full below.

Full description from employer

We are seeking a Regulatory Affairs Manager to support our local Regulatory Team in Zug. You will oversee the submission strategy for new medicinal products and manage the lifecycle of existing ones, ensuring compliance with local regulations. Ideal candidates have significant regulatory experience in Switzerland and strong analytical and communication skills.

Skills

  • regulatory affairs
  • marketing authorization submission
  • german language proficiency
  • life cycle management
  • regulatory compliance
  • promotional material review
  • pharmacode compliance
  • e-ctd submissions
  • stakeholder management
  • english language proficiency
  • pharmacy degree
  • medicine degree
  • natural sciences degree
  • teamwork
  • strategic thinking
  • analytical skills

Company

Merck KGaA
Zug, Switzerland

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from Merck KGaA·first seen 24 Sept 2026·last verified 24 Sept 2026·How we source jobs

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