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Regulatory Affairs Manager (a)

Michael Page International (Switzerland) SA

Baar

Hybrid

EUR 60.000 - 80.000

Vollzeit

Heute
Sei unter den ersten Bewerbenden

Zusammenfassung

A leading recruitment company is seeking an RA Manager in Baar, Germany. This role involves preparing and submitting regulatory documentation, ensuring compliance, and collaborating with cross-functional teams. Candidates should have a background in Life Sciences and experience in regulatory affairs. The position offers a hybrid work model and the chance to contribute to impactful projects.

Leistungen

Access to industry-leading resources and tools
Professional and supportive working environment

Qualifikationen

  • Proficiency in English, both written and spoken; additional languages are a plus.
  • Proven experience (3-5 years) in regulatory affairs within the LIFE SCIENCE industry.
  • Strong knowledge of relevant regulatory guidelines and processes.

Aufgaben

  • Develop and execute regulatory strategies to support product approvals.
  • Ensure alignment of regulatory activities with global and local requirements.
  • Collaborate with cross-functional teams to support regulatory submissions.
  • Monitor and interpret regulatory guidelines.
  • Maintain regulatory records and manage documentation systems.

Kenntnisse

Regulatory strategy development
Compliance monitoring
Team collaboration
Excellent communication

Ausbildung

Educational background in Life Sciences or related field
Jobbeschreibung
  • Prestigious, global player in biotechnology
  • 7 months contract with extension option
About Our Client

Our client is a medium-sized enterprise within the LIFE SCIENCE industry, known for its innovative approach and commitment to excellence. They focus on delivering high-quality solutions and maintaining compliance within a regulated environment. Hybrid work model.

Job Description

As RA Manager your focus will be on preparing, reviewing, and submitting regulatory documentation to relevant authorities. On top you will also be responsible for the following task areas:

  • Develop and execute regulatory strategies to support product approvals and compliance.
  • Ensure alignment of regulatory activities with global and local requirements.
  • Collaborate with cross-functional teams to support regulatory submissions.
  • Monitor and interpret regulatory guidelines to ensure compliance.
  • Maintain regulatory records and manage documentation systems effectively.
  • Act as a point of contact for regulatory agencies and internal stakeholders.
  • Support the team in implementing best practices and continuous improvements in regulatory processes.
The Successful Applicant

A successful REGULATORY AFFAIRS MANAGER should have:

  • Educational background in LIFE SCIENCES or a related field.
  • Proficiency in English, both written and spoken; additional languages are a plus.
  • Proven experience (3-5 years) in regulatory affairs within the LIFE SCIENCE industry.
  • Strong knowledge of relevant regulatory guidelines and processes.
  • Excellent organizational and communication skills.
  • Ability to work collaboratively in a cross-functional team environment.
What's on Offer

Our client offers you:

  • An engaging temporary role in Baar within the LIFE SCIENCE industry.
  • Opportunities to contribute to impactful projects and regulatory success.
  • A professional and supportive working environment.
  • Access to industry-leading resources and tools.

If you are ready to make a significant impact as a REGULATORY AFFAIRS MANAGER, we encourage you to apply today

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