Intern: Environmental Compliance

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.

Join Roche, where every voice matters.

Help shape the future of sustainable healthcare.

Global chemical and environmental regulations play a vital role in every stage of a product's lifecycle - from development and manufacturing to usage and disposal. At Roche Pharma Technical Operations, we are uniting our expertise and expanding our capabilities to ensure strong compliance with these important regulations.

In this role, you will work directly alongside our Environmental Regulatory Experts to navigate highly complex global chemical policies, contributing to the compliance and sustainability of our life-saving products.

This internship offers a unique opportunity to gain hands‑on experience in global environmental regulatory affairs within a leading pharmaceutical setting. Supported by senior experts, you will drive specific initiatives, including:

• Regulatory Analysis & Impact Mapping:
  Monitor and analyze key global and regional regulations (such as EU/China REACH, Biocides, and EPR) to assess and document their impact on Roche Pharma operations
• Dossier & Registration Support:
  Collaborate with internal stakeholders and technical experts (e.g., ecotoxicologists) to gather data required for chemical and biocide registration dossiers
• External Study & Compliance Monitoring:
  Assist in tracking and monitoring testing studies conducted by external service providers for global chemical regulations
• Compliance Framework Development:
  Support the definition and digital implementation of a standardized global compliance oversight tool to ensure operational adherence
• Cross-Functional & Divisional Engagement:
  Actively participate in projects involving Pharma Sites, Diagnostics, and Diabetes Care to foster regulatory alignment and knowledge sharing

• You are currently enrolled in, or have graduated from, a Master's degree program in Environmental Regulations, Bio-engineering, Medical technical engineering Law with a focus on Env Law or Regulatory compliance, Chemistry or Chemical engineering (with knowledge of product regulations). Masters can be recently graduated within the last 12 months of starting the internship. PhD students must be enrolled for the entire duration of the internship

• Analytical skills:
  Ability to analyse complex regulations and regulatory guidance documents and translate them into easily understandable concepts.
• Strong
  
  Collaboration:
  
  Team player who is comfortable working in a matrixed, multinational environment and building networks across different global sites
• Communication & Presentation:
  Fluent in English (written and verbal) with an aptitude for presenting complex technical data clearly
• Proactive & Independent:
  Self-motivated to take ownership of tasks and drive them to completion with guidance from mentors and subject matter experts
• Digital Proficiency:
  Strong competency with Google and or Microsoft Workspace, AI tools, and data analysis software, with an aptitude for working with regulatory compliance databases

• Due to regulations, non-EU/EFTA citizens must be actively enrolled for the entire duration of the internship and provide an official university certificate stating that the internship is a mandatory part of their studies
• This internship position is located in Basel
• The…