Technical Regulatory Associate

Johnson & Johnson MedTech

Latina, Italy
Quality systems
Technical regulatory
Change control
The role is responsible for ensuring product quality conforms to current specifications and regulations (GMP) through the verification of standard operating procedures and the use of appropriate tools

Job Summary

  • The role is responsible for ensuring product quality conforms to current specifications and regulations (GMP) through the verification of standard operating procedures and the use of appropriate tools.
  • Responsibilities include preparing international and local registration documentation, collecting and processing required information and certifications, and compiling regulatory master data.
  • The company aims to create an inclusive work environment where each person is considered an individual, respecting diversity and dignity.

Matching Summary

The role is responsible for ensuring product quality conforms to current specifications and regulations (GMP) through the verification of standard operating procedures and the use of appropriate tools.

Skills & Requirements

Must-have

  • Quality Systems
  • Technical Regulatory
  • Change Control
  • GMP compliance
  • International registration documentation

Nice-to-have

  • Accountability
  • Analytical Reasoning
  • Communication
  • Process Oriented
  • Data Savvy

Key Requirements

  • Master's degree in Chemistry and Pharmaceutical Technology, Pharmacy, Chemistry, or Biology
  • 12 months of experience in the pharmaceutical sector or similar
  • Excellent knowledge of English
  • Good knowledge of the Office package

Work Rights

Not specified

Tailored Resume

Cover Letter