Regulatory Affairs Expert

vor 4 Wochen


Hamburg, Hamburg, Deutschland GULP – experts united Vollzeit

At GULP – experts united, we're actively shaping the future of our clients and benefiting from our exclusive network. Our global leader in skin care, cosmetics, and wound care is looking for a Regulatory Affairs Specialist to join their team in the Hamburg area.

As a Regulatory Affairs Specialist, you'll drive your professional development in an innovative environment. You'll have the opportunity to take on a wide range of responsibilities, including planning and coordination of global product approvals, development and implementation of approval strategies, and ensuring compliance with international regulations.

Here's what we offer:

  • Attractive salary and long-term job security through group affiliation
  • Up to 30 days vacation per year
  • Contribution to company pension scheme after end of probationary period
  • Extensive social benefits, including Christmas and vacation bonuses
  • Reimbursement of travel expenses
  • Generally an open-ended employment contract
  • Good chances of being taken on by our business partners
  • Tailored further training opportunities and free language courses
  • A wide range of employee benefits

As a Regulatory Affairs Specialist, you'll be responsible for:

  • Planning and coordination of global product approvals
  • Development and implementation of approval strategies
  • Ensuring compliance with international regulations
  • Compilation and review of approval documents
  • Coordination with authorities and stakeholders
  • Main contact person for registration issues
  • Establishing and maintaining an administrative system for product approvals
  • Regular updates to ensure compliance with regulations
  • Initiation and management of digitalization projects
  • Implementation of digital tools to increase efficiency

What we're looking for:

  • Completed scientific or technical studies
  • Several years of experience in the approval of regulated products
  • Knowledge of drug approval is an advantage
  • Sound knowledge of international regulations and standards
  • Strong project management skills, especially for parallel projects
  • Very good written and spoken English skills
  • SAP knowledge is an advantage
  • Good knowledge of digital tools for regulatory processes
  • High attention to detail and organizational skills
  • Ability to work in multicultural teams


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