Regulatory Program Manager

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:

Are you ready to innovate, collaborate, and create impactful outcomes? Join us as a Regulatory Program Manager in the Pharma Technical Regulatory Submission Management Group. In this role, you will play a pivotal part in global planning, tracking, and monitoring of regulatory information crucial for compliance and successful submission execution.

You will:

1. Manage regulatory information activities in coordination with the regulatory product portfolio team.
2. Partner with various departments to ensure seamless submission processes.
3. Oversee the formatting (and editing) of technical documents.
4. Coordinate document flow within the management system and ensure version control throughout the submission process.
5. Ensure timely delivery of content and maintain clear communication with technical subject-matter experts.

Who You Are:

1. A graduate with a Bachelor's or higher degree in biology, chemistry, English, or a related field.
2. Proficient in document management best practices and comfortable with diverse digital tools.
3. Skilled at building productive relationships across departments and with external partners, thriving in a diverse team.
4. An effective problem-solver with excellent interpersonal skills, able to prioritize multiple tasks.
5. Committed to continuous improvement, always looking for ways to enhance processes, systems, and tools, and open to giving and receiving feedback.
6. Experience with Veeva Vault RIM is desirable.

Join us and be part of a team dedicated to making a difference for patients, stakeholders, and our company. Apply now and help us drive innovation in regulatory submissions!

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.

Our UK Pharmaceutical head office is situated in Welwyn Garden City, Hertfordshire, with beautiful countryside surrounding the area. Supported by major motorways & airports as well as being a 30 minute train ride to London, access is easy. Our award-winning office, known as Hexagon Place, was opened in 2005 and provides a modern, flexible working environment with facilities that are second-to-none. Around 2,000 people work at our Welwyn office in Global Early Development (pRED), Global Product Development (PD), Commercial (Rx) and our Corporate functions.

Roche offers a competitive salary plus the excellent benefits you would expect from a blue-chip organisation. There is a fully equipped gym on-site, a library and information centre, and an active sports and social club. We also have a subsidised staff restaurant providing foods to cater for every taste throughout the day. At the heart of the building is an informal meeting area known as The Street which features a coffee shop, snack machine and cashpoint. A second building on-site, called The Hub, contains modern meeting room and conference facilities. Roche promotes personal well-being and work-life balance. Therefore, flexible working options will be considered for all roles at Roche UK. Roche is committed to creating a diverse & inclusive environment.