EEMEA Regulatory Policy Associate

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.

The Position

The Opportunity

We are seeking a highly motivated and detail-oriented individual to join our team as a Regulatory Policy Associate. In this dynamic role, you will play a critical part in enhancing our regulatory intelligence and policy advocacy across the EEMEA region.

Main Responsibilities

- Conducting comprehensive intelligence digests and analyses to create insightful dashboards, slides, and summaries, capturing key regulatory updates within the EEMEA region internally and externally.

- Assisting in the empowerment program ( capability building program) by converting global strategies into effective training materials for local affiliates, and developing cross-country comparison insights that leverage your understanding of diverse local landscapes.

- Facilitating the operation of the EEMEA Regulatory Policy Community of Practice, including organizing meetings, agenda creation,  documenting minutes, coordinating with members, and managing project-based teams ("topic-based squads").

- Enhancing the communication of regulatory policy value through the creation of supportive visual materials for the leadership team, maintaining the EEMEA regulatory policy Community of Practice web page, crafting success story visuals and summaries, and assisting with various external and internal events.

- Contributing to research efforts and connecting with internal stakeholders for the development of regional and local position papers on a variety of topics, ensuring that our regulatory stances are well-informed and robust.

- Supporting the Regradar regulatory monitoring tool by ensuring that regulatory cases are thoroughly evaluated and assessed within specified timelines, maintaining high standards of compliance and awareness.

Who you are

Required experience and competencies
- A minimum of 3 years of experience in regulatory - within medtech industry is a plus

- Experience in project management and the ability to manage multiple priorities in a fast-paced environment.

- Familiarity with regulatory policy frameworks and a keen interest in staying updated with global regulatory trends is a plus

- Strong analytical skills and the ability to interpret complex regulatory information.

- Excellent communication skills, both written and verbal, with proficiency in creating clear and compelling presentations.

NOTE: This role is a contractor, the employment agreement will be signed through a third party agency

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.