Regulatory Affairs Specialist
il y a 2 semaines
At Lonza, we are seeking a talented Regulatory Affairs Professional to join our team in the Capsules & Health Ingredients business. As a key member of our team, you will be responsible for anticipating, capturing, and assessing regulatory requirements in the healthcare industry, including excipients, pharmaceuticals, and food manufacturing.
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 degree or similar in pharmacy, chemistry, bio engineering, biotechnology, or food technology.
- 2-3 years of experience in RA within the food industry.
- Knowledge of GMP requirements.
- Fluent in English and French.
- Strong communication skills and attention to detail.
At Lonza, we value our people and our environment. We strive to achieve our business results in an ethical and responsible manner. If you are a motivated and detail-oriented individual with a passion for regulatory affairs, we encourage you to apply for this exciting opportunity.
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