Senior Counsel - Regulatory

Job not on LinkedIn

June 28

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Logo of Avantor

Avantor

Science • Biotechnology • Healthcare Insurance

Avantor is a leading life science tools company and global provider of mission-critical products and services to the life sciences and advanced technology industries. The company collaborates with scientists around the world to enable breakthroughs in medicine, healthcare, and technology. Avantor offers a proven portfolio of trusted, quality brands used in research, development, and production activities across more than 300,000 customer locations in 180 countries. It focuses on supporting scientific journeys through reliable products, digital solutions, innovation, and manufacturing facilities. Avantor is committed to sustainability, advancing biopharma, and enhancing scientific collaboration with digital technologies.

10,000+ employees

Founded 1904

🔬 Science

🧬 Biotechnology

⚕️ Healthcare Insurance

đź“‹ Description

• Provide expert legal advice and guidance to senior management and legal colleagues on European regulations, directives, and policies impacting the business, including REACH, CLP, MDR/IVDR, GMP guidelines, pharmaceutical and/or medical device law, regulations and guidance related to the development of and commercialization of products, import/export law and environmental regulations. • Develop and implement compliance strategies to ensure adherence to European regulatory requirements including adherence to EU and international trade regulations, including customs classifications, Incoterms, duty drawback processes, and trade sanctions. • Collaborate with internal and external stakeholders, including government bodies, industry associations, and cross-functional teams, to address regulatory issues. • Conduct training sessions to enhance awareness of regulatory requirements within the organization.

🎯 Requirements

• 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. • Law degree (LLM or equivalent) and registered as an attorney in at least one European jurisdiction. • Strong analytical and problem-solving abilities, excellent communication and negotiation skills, and the ability to work effectively in cross-functional teams. • Proficiency in English is required and at least one other European language is preferred.

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