Regulatory Specialist

Zentiva Group, a.s

Warsaw, Poland
Hybrid
European registration procedures mrp dcp cp
National phase registration coordination
Medical product labeling verification
Zentiva Group is seeking a Regulatory Specialist in Warsaw, Poland, to oversee the registration processes of medicinal products in European procedures. The ideal candidate should possess a relevant degree, at least three years of experience in regulatory affairs, and strong English language skills

Job Summary

  • The role involves overseeing new medicinal product registrations within European procedures including MRP, DCP, and CP.
  • Candidates will coordinate national registration phases and verify graphic projects for drug leaflets and packaging.
  • The position requires ensuring proper communication with local regulatory authorities and collaborating with central RA departments.

Matching Summary

Match Score: 85

Zentiva Group is seeking a Regulatory Specialist in Warsaw, Poland, to oversee the registration processes of medicinal products in European procedures. The ideal candidate should possess a relevant degree, at least three years of experience in regulatory affairs, and strong English language skills.

Skills & Requirements

Must-have

  • European registration procedures MRP DCP CP
  • National phase registration coordination
  • Medical product labeling verification
  • Post-registration change implementation
  • English language proficiency required

Nice-to-have

  • Strong organizational and prioritization skills
  • Problem-solving and independent action
  • High interpersonal and team collaboration skills
  • Meticulous attention to detail and punctuality

Key Requirements

  • Higher education in pharmaceutical, medical, chemical, or biological fields
  • Minimum 3 years experience in European and national registration processes
  • Fluency in English speaking and writing
  • Knowledge of pharmaceutical law and required documentation

Work Rights

Not specified

Tailored Resume

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