Regulatory Affairs Team Lead - 12 months mission

Michael Page; Genf; Vor Ort; CHF 80’000 - 120’000; Vollzeit

Zusammenfassung

A leading company in Geneva is seeking a Regulatory Affairs Team Lead for a 12-month mission. The ideal candidate will gain valuable experience in a globally recognized healthcare firm, developing regulatory expertise while coordinating with various departments, ensuring compliance with Swissmedic and EU regulations.

Leistungen

Collaborative and supportive team environment

Exposure to international regulatory processes

Competitive compensation

Qualifikationen

• 2 years of experience in Regulatory Affairs within healthcare/pharmaceutical/medical device industry.
• Familiarity with Swiss and EU regulatory frameworks.
• Fluency in English; French is a strong asset.

Aufgaben

• Support the Regulatory Affairs team in preparing and tracking regulatory documents.
• Coordinate with internal departments to gather necessary documentation.
• Ensure compliance with regulatory requirements.

Kenntnisse

Organizational skills

Communication skills

Ausbildung

Bachelor's degree in Life Sciences, Pharmacy, or related field

Tools

Microsoft Office

Regulatory tracking tools

Jobbeschreibung

Regulatory Affairs Team Lead - 12 months mission

Join to apply for the Regulatory Affairs Team Lead - 12 months mission role at Michael Page

Regulatory Affairs Team Lead - 12 months mission

Join to apply for the Regulatory Affairs Team Lead - 12 months mission role at Michael Page

• Gain valuable experience in a globally recognized healthcare company
• Develop your regulatory expertise through hands-on experience
  
  

• Gain valuable experience in a globally recognized healthcare company
• Develop your regulatory expertise through hands-on experience
  
  

About Our Client

Our client a healthcare company in Geneva.

Job Description

• Support the Regulatory Affairs team in the preparation, submission, and tracking of regulatory documents.
• Coordinate with internal departments (Quality, Clinical, R&D, Marketing) to gather necessary documentation.
• Maintain regulatory databases and ensure timely updates of product information.
• Assist in compiling dossiers for product registrations, renewals, and variations in compliance with Swissmedic and EU regulations.
• Monitor regulatory timelines and ensure adherence to submission deadlines.
• Liaise with health authorities and third-party partners as needed.
• Ensure compliance with internal SOPs and applicable regulatory requirements.
  
  

The Successful Applicant

• Bachelor's degree in Life Sciences, Pharmacy, or a related field.
• Minimum 2 years of experience in Regulatory Affairs within the healthcare, pharmaceutical, or medical device industry.
• Familiarity with Swiss and EU regulatory frameworks.
• Strong organizational and communication skills.
• Proficiency in Microsoft Office and regulatory tracking tools.
• Fluent in English; French is a strong asset.
  
  

What's on Offer

• A collaborative and supportive team environment.
• Exposure to international regulatory processes.
• Opportunity to work with a reputable healthcare company in Geneva.
• Competitive compensation through Michael Page.
  
  

Contact: Aurélien Monchambert

Quote job ref: JN-062025-6759061

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science and Health Care Provider

• Industries

  Staffing and Recruiting

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