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Regulatory Affairs Specialist
Il y a 2 mois
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.
- 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.