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Regulatory Affairs Specialist

Il y a 2 mois


Colmar, Grand Est, France Lonza Temps plein
Join Our Team as a Regulatory Affairs Specialist

Lonza, a global leader in life sciences, is seeking a talented Regulatory Affairs Specialist to anticipate, capture, and assess regulatory requirements in the healthcare industry. As a key member of our team, you will play a crucial role in ensuring continued compliance and sustaining market recognition as a compliant business partner in a regulated environment.

Key Responsibilities:
  • Anticipate and capture regulatory evolutions in areas of interest, including legislative changes and industry guidance.
  • Draw up documented regulatory impact assessments and translate applicable regulations into comprehensive action plans.
  • Create and maintain relevant documentation, registration files, and standard operating procedures.
  • Actively support EMEA customers and authority requests related to regulatory requirements.
  • Support marketing, R&D, and Lonza BU in ad hoc projects related to market growth and innovation initiatives.
Requirements:
  • Master's degree or similar in pharmacy, chemistry, bioengineering, biotechnology, or food technology.
  • 2-3 years of experience in RA within the food (supplements) industry.
  • Knowledge of GMP requirements.
  • Fluent in English and French.
  • Strong communication skills and attention to detail.

Lonza is committed to improving lives worldwide through innovative products and services. As a Regulatory Affairs Specialist, you will have the opportunity to make a meaningful difference in the lives of millions of people. If you are passionate about regulatory compliance and have a strong desire to contribute to a global leader in life sciences, we encourage you to apply for this exciting opportunity.