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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.
The Senior Legal Counsel will provide strategic and operational legal advice to the Packaging, Paper, and Recycling businesses across Central EMEA. Responsibilities include drafting complex agreements, managing regulatory compliance, overseeing M&A transactions, and coordinating with external law firms.
The Contract Manager oversees a portfolio of client contracts, ensuring technical maintenance, safety compliance, and operational profitability. They are responsible for managing technical teams, handling budgets, and maintaining strong client relationships.
The Associate Director will lead EU regulatory strategy and provide expert guidance throughout the product lifecycle, from preclinical stages to post-approval. They will act as a key liaison between internal teams and regulatory authorities to ensure high-quality, timely submissions and compliance.
The Regulatory Affairs Scientist supports the development and execution of global and regional regulatory strategies for clinical programs. They contribute to the compilation of regulatory submissions and collaborate with cross-functional teams to manage Health Authority interactions and regulatory risks.
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The Regulatory Liaison acts as the primary interface for clinical trial teams, ensuring compliance with global and local regulations throughout the trial lifecycle. They are responsible for preparing and coordinating regulatory submission packages and maintaining transparency in clinical trial activities.
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.
You will own and scale the global internal IT roadmap, architecture, and standards, including identity management and device compliance. Additionally, you will manage IT-related compliance controls, risk management, and audit readiness to ensure a secure and scalable environment.
The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving global regulations. They will also act as a key point of contact for regulatory authorities and provide strategic guidance to project teams.
The intern will monitor and interpret complex renewable energy and carbon pricing regulations to provide actionable market insights. They will collaborate with traders and compliance teams to quantify credit opportunities and maintain regulatory databases.
The Regulatory Affairs Specialist will manage CMC compliance activities, including change controls, deviations, and regulatory submissions. They will collaborate with cross-functional teams to ensure product registrations and documentation meet global regulatory requirements.
The Global Regulatory Lead will develop and execute global regulatory strategies while serving as a key business partner for product life cycle management. This role involves coordinating regulatory filings, overseeing vendors, and ensuring timely compliance with global health authority requirements.
The Regulatory Liaison acts as the primary interface for clinical trial teams, ensuring compliance with global and local regulations. They are responsible for preparing, reviewing, and coordinating regulatory submission packages while maintaining transparency throughout the trial lifecycle.
Lead the global data privacy strategy and framework while providing strategic leadership on compliance and risk management. Advise senior leadership on data privacy obligations and drive a privacy-by-design culture across the organization.
Manage and oversee contractual aspects of clinical trials, including drafting and negotiating high-value agreements like CTAs and CDAs. Ensure compliance with international regulations and provide guidance to project teams and junior specialists.
The role involves drafting and maintaining cyber insurance policies and managing distribution partnerships for the Belgian market. Additionally, the manager will handle cyber claims and produce reporting for risk carriers.
Manage site activation activities and serve as the single point of contact for investigative sites and project management teams. Ensure all regulatory, ethics, and contractual documents are accurately prepared and executed according to project timelines.
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Oversee global intellectual property litigation strategy and enforce Standard Essential Patents (SEPs) across various technology sectors. Manage external counsel and collaborate with internal departments to handle budgets and support licensing settlement negotiations.
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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