Working Student (mfd) Global Regulatory Affairs

Merz Therapeutics

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profile Job Location:

Frankfurt am Main - Germany

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

YOUR CONTRIBUTION

Within our Global Regulatory Affairs departmentyou will support the implementation of our new DMS (Document Management System) by migrating data files. Together with you we will ensure our regulatory processes and contribute to the achievement of our corporate goals. We offer you exciting insights into the regulatory processes of an international pharmaceutical company. Your tasks with us include in particular:

  • Supporting Regulatory Experts in international submissions

  • Supportfile management in an electronic data management system

  • Support update of file naming in excel sheets for migration of products to an electronic data management system
  • Support CMC Manager in updating CMC dossiers for variations

  • Completing database entries and checking them for completeness

YOUR PROFILE

  • Studies in natural sciences (e.g. Pharmacy Chemistry Biology or related courses)

  • Basic understanding of Chemistry Analytics and Manufacturing

  • A good level of German and English is required

  • Confident and assured handling of Microsoft Office

  • Advanced knowledge of Microsoft Excel and at least first experiences with databases are an advantage

YOUR BENEFITS

  • Exciting projects and a lot of personal responsibility from day one

  • Cooperation in multifunctional and global teams

  • Flexible working hours and other employee benefits

  • Attractive remuneration

  • An open and international working environment in a global family business

Find out more about our benefitshere.

ABOUT US

Welcome to Merz Therapeuticsa leading pharmaceutical company that helps people with movement disorders neurological diseases liver diseases and other health conditions regain their quality of life.

We are proudto be a family-owned and value-driven company that has been dedicated to serving the needs of our patients for 110 years and is now a global innovation leader with products in more than 90 countries.

Our goalis to use our products to improve treatment outcomes for patients around the world thereby reducing the burden of suffering for affected people and their surroundings.

Our dedication and commitmentto relentless research and development is to ensure that unmet patient needs are identified and appropriate treatments are provided.

Therefore become part of our international and motivated Merz Therapeutics family now and help us achieve our goal: BETTER OUTCOMES FOR MORE PATIENTS


Required Experience:

Unclear Seniority

YOUR CONTRIBUTIONWithin our Global Regulatory Affairs departmentyou will support the implementation of our new DMS (Document Management System) by migrating data files. Together with you we will ensure our regulatory processes and contribute to the achievement of our corporate goals. We offer you ex...
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Key Skills

  • Proofreading
  • Adobe Acrobat
  • FDA Regulations
  • Manufacturing & Controls
  • Biotechnology
  • Clinical Trials
  • Research & Development
  • GLP
  • cGMP
  • Product Development
  • Chemistry
  • Writing Skills

About Company

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Innovative solutions in the therapeutic field of Neurology.

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