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The specialist will drive global regulatory strategy by providing intelligence, managing advocacy initiatives, and supporting innovation programs. They will act as a liaison between regulatory, R&D, and commercial teams to manage risks and ensure compliance across the global product portfolio.
Provide hands-on legal operations support across EU jurisdictions, including contract drafting and employment law guidance. Act as the named Responsible Person for the Swiss entity to ensure compliance with labour-leasing laws and SECO requirements.
Analyze and research complex legal matters including corporate, employment, and regulatory issues. Evaluate AI-generated legal content for accuracy and assist in the development and validation of legal datasets.
Provide expert legal analysis on the EU AI Act, GDPR, and data governance to support AI model training and compliance. Identify legal inaccuracies in AI-generated responses and develop structured legal reasoning and evaluation criteria.
Analyze and research corporate, employment, and regulatory legal matters while reviewing contracts and documentation. Annotate legal datasets and evaluate AI-generated legal reasoning for accuracy and compliance.
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The Senior Corporate Counsel will serve as a strategic legal partner, managing complex international commercial and operational legal matters across multiple markets. This role involves drafting and negotiating commercial agreements, providing risk-based advice to business leaders, and supporting regulatory and compliance initiatives.
Legal fellows will conduct research on complex legal questions, draft licensing agreements, and develop internal and external policies. They will work under the supervision of an attorney to support the Foundation's legal department on various projects.
The Senior Trade Compliance Analyst manages import and export compliance operations, including customs classification, licensing, and sanctions screening for the EU, UK, and Switzerland. This role acts as the primary point of contact for trade compliance matters, ensuring adherence to regional regulations and supporting internal stakeholders.
You will prepare and organize legal documents such as contracts and resolutions while systematically utilizing AI tools in daily workflows. Additionally, you will conduct research and ensure the quality and accuracy of AI-generated outputs for the legal team.
The Senior Manager will oversee global IP strategy for biosimilar products and manage multi-country patent litigations. They will also provide legal advice on complex IP landscapes and guide the Freedom to Operate design for new products.
Negotiate and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials. Ensure compliance with SOPs and regulatory guidelines while collaborating with legal and project management teams.
Responsible for ensuring compliance with dangerous goods and transportation regulations across European sites, specifically implementing the EU-PIC regulation. The role involves managing export notifications, auditing safety data sheets, and developing training programs for hazardous materials management.
Support clinical research, physician engagement, and global regulatory strategies to advance breakthrough cardiac therapies. Manage the development and commercialization of biomimetic TAVR valves and anti-calcification technologies.
The Contract Specialist oversees procurement processes and ensures strict compliance with federal and GSA regulations. Key duties include preparing solicitation documents, conducting cost analysis, and managing the full lifecycle of contract administration and closeout.
Manage the end-to-end global labelling lifecycle, including preliminary assessment, implementation, and post-approval maintenance. Collaborate with regional teams to ensure compliance with country-specific regulatory requirements and maintain labelling databases.
Ensure compliance with laws and regulations in Switzerland and Liechtenstein by implementing policies and conducting risk assessments. Act as the Money Laundering Reporting Officer (MLRO) to oversee AML obligations and represent the firm to regulatory authorities.
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The Director will develop and execute regional CMC regulatory strategies to support clinical development, marketing authorizations, and lifecycle management in Europe. They will serve as the primary lead for interactions with the EMA and national competent authorities while providing strategic guidance across cross-functional teams.
The Managing Counsel will lead AI and HRIS product compliance, embedding risk-based legal reviews into product development workflows. They will also own product terms and conditions for HRIS and AI features while partnering with engineering, security, and privacy teams.
The role involves planning, preparing, and revising regulatory documents for various submissions, ensuring accuracy and compliance with regulations. It also includes collaborating with internal teams to author CMC regulatory content and providing assessments for manufacturing changes.
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