Regulatory Affairs Specialist, 50%, 1-year Contract

Johnson & Johnson Johnson & Johnson · Pharma · Zagreb, Croatia

This role is for a Regulatory Affairs Specialist at Johnson & Johnson, focusing on regulatory activities for the Innovative Medicine portfolio in Croatia. Responsibilities include collaborating on regulatory submissions, ensuring compliance with local and EU regulations, and supporting audits. The role requires a university degree in life sciences and 2-4 years of experience in Regulatory Affairs within the pharmaceutical/biotechnology industry, with strong knowledge of Croatian and EU legislation.

What you'd actually do

  1. Partners with local RA team with regards to regulatory activities for the Johnson & Johnson Innovative Medicine portfolio
  2. Collaborate with cross-functional regional/global and in country teams to ensure timely and quality regulatory submissions, including review and approval of regulatory documents and labeling and to align strategies and share best practices
  3. Monitor and interpret local regulatory requirements and guidelines in Croatia, providing guidance and training to ensure compliance
  4. Support regulatory inspections and audits and facilitate timely resolution of any regulatory issues or deficiencies
  5. Ensure compliance with local regulatory requirements and company standards.

Skills

Required

  • University degree or equivalent in life sciences field or a related field
  • Proven experience in Regulatory Affairs within the pharmaceutical/biotechnology industry (at least 2-4 years in industry field)
  • Solid understanding of regulatory requirements and procedures in Croatia and EU legislation.
  • Excellent understanding of the drug development process, including clinical trials, pharmacovigilance, and post-market surveillance.
  • Ability to effectively communicate regulatory information to diverse partners, both internally and externally.
  • Profound English language skills
  • High attention to details and analytical skills (e.g., systems, documentation, metrics)
  • Ability to independently plan, organize, co-ordinate, proactively lead and execute tasks

What the JD emphasized

  • Proven experience in Regulatory Affairs within the pharmaceutical/biotechnology industry (at least 2-4 years in industry field)
  • Solid understanding of regulatory requirements and procedures in Croatia and EU legislation.