Regulatory Affairs Specialist

il y a 1 semaine


Colmar, Grand Est, France Lonza Temps plein

At Lonza, we are seeking a Regulatory Affairs Specialist to join our team in the Capsules & Health Ingredients business. This role will be responsible for anticipating, capturing, and assessing regulatory requirements in the healthcare industry, with a focus on excipient, pharmaceutical, and food manufacturing.

Key Responsibilities:

  • Anticipate and capture regulatory evolutions in areas of interest, including legislative evolutions 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 degree or similar in pharmacy, chemistry, bio engineering, 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.

At Lonza, we are committed to improving lives through innovative products and services. Our Regulatory Affairs Specialist will play a critical role in ensuring our compliance with regulatory requirements and maintaining our position as a trusted partner in the industry.



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