Manager of Regulatory Affairs

vor 4 Wochen

Frankfurt am Main, Hessen, Deutschland Merz Therapeutics Vollzeit
Manager of Regulatory Affairs (m/f/d) CMC

Position Summary:

  • Accountable for leveraging expertise in global regulatory quality standards to facilitate the approval and ongoing compliance of pharmaceutical products.
  • Responsibilities encompass the creation, assessment, and revision of CMC documentation, executing change control protocols, addressing inquiries from regulatory bodies, orchestrating projects, formulating regulatory strategies, and remaining updated on international regulatory standards.

Qualifications:

  • Educational background in Pharmacy, Biology, or Chemistry.
  • 3-5 years of professional experience in regulatory affairs or CMC-related fields.
  • Exceptional communication, analytical, and negotiation abilities.
  • Commitment to compliance and quality assurance.

Company Overview:

Merz Therapeutics stands as a prominent pharmaceutical entity dedicated to enhancing the quality of life for individuals facing movement disorders, neurological conditions, and various health challenges. With a legacy spanning over 110 years, Merz Therapeutics is recognized as a global leader in innovation, committed to delivering effective treatments for patients across the globe.

Employee Benefits:

  • Career advancement opportunities.
  • Hybrid work model promoting work-life balance.
  • Modern workplace facilities and company dining options.
  • Global family-owned business fostering a respectful corporate culture.
  • Competitive remuneration and comprehensive social benefits.

Join Merz Therapeutics to contribute to our mission of 'Better Outcomes for More Patients.'

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