Education: Law degree (LLM or equivalent) and registered as an attorney in at least one European jurisdiction.
Experience: 10+ years of legal experience, preferably from working for a leading law firm and/or multinational corporation, with 5-7 years of experience specializing in European regulatory law within the pharmaceutical, chemical, medical device or other highly regulated industries. Experience collaborating across a matrixed business and legal environment.
Expertise: In-depth knowledge of EU regulatory frameworks, including CLP, REACH, and GMP guidelines.
Skills: Strong analytical and problem-solving abilities, excellent communication and negotiation skills, and the ability to work effectively in cross-functional teams.
Languages: Proficiency in English is required and at least one other European language is preferred.