One Product Development Regulatory (PDR) Early Talent (ET) Program (Basel, 2 years)

Roche; Basel; On-site; CHF 90,000 - 120,000; Full time

Job summary

Roche is offering a two-year Early Talent program in Regulatory Affairs that blends hands-on assignments with tailored learning. It provides exposure to the full lifecycle of pharmaceutical products and rotating opportunities within PDR.

ETs work with global teams, developing scientific writing skills and preparing regulatory documents for Health Authority interactions. The program emphasizes learning, ownership of development, and collaboration across seasonal therapeutics, with a strong

Qualifications

• Degree in life sciences or related field completed within the expected timeframe.
• No more than 1 year of pharma experience after last degree.
• Basic understanding of drug development and regulatory roles.
• Willingness to learn, accept feedback and grow professionally.

Responsibilities

• Build foundational regulatory experience through mentored regulatory projects.
• Learn drug development processes and regulatory roles across teams.
• Prepare regulatory documents and support health authority interactions.
• Collaborate with global product development regulatory teams and stakeholders.
• Develop business process understanding to deliver regulatory deliverables.
• Spend significant time on-site at Roche offices and participate in reviews.

Skills

Learning mindset

Team collaboration

Autonomy

Education

B.Sc., M.Sc., or PhD in life sciences/biology/chemistry/pharmacy

Job description

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

Embark on a transformative two-year journey with the One Product Development Regulatory (PDR) Early Talent (ET) Program, meticulously crafted to impart comprehensive foundational knowledge in regulatory affairs. This dynamic initiative blends hands‑on assignments with tailored learning solutions, making it an ideal entry‑point for aspiring regulatory professionals. Participants gain invaluable insights into the complete lifecycle of pharmaceutical products, from initial clinical trials to market exit, by engaging in diverse activities across various therapeutic areas and stages of development. The latter part of the program offers the opportunity to rotate into another function or specialize further in PDR.

Throughout the program, ETs collaborate with global drug development teams to support the introduction of novel pharmaceutical products to patients worldwide. This environment not only enhances their scientific writing skills but also deepens their understanding of regulatory frameworks by preparing a wide array of regulatory documents and supporting Health Authority Interactions.

The opportunity

• Actively build foundational regulatory experience through your work on regulatory projects with the appropriate mentorship
• Take ownership of your learning and development, actively seeking to understand drug development and regulatory roles, and engaging in knowledge sharing and peer support
• Become responsible for understanding and applying business processes to deliver foundational regulatory deliverables
• Engage with regulatory and cross functional teams through active listening, practicing open communication, and building trust with global team members
• Grasp the vision of the Roche organization, understanding how your work impacts the team and contributes to overall goals
• Improve prioritization and time management skills while spending significant time on-site at the Roche office

Who you are

You hold a degree (B.Sc., M.Sc., or PhD) in a life sciences, biological sciences, biology, chemistry, pharmacy, or related field before the start of the program, and you are within two years of completion of a degree program in the before mentioned disciplines. Furthermore, you have:

• no more than 1 year of relevant past pharmaceutical experience post last degree
• a basic understanding of drug development and entry level understanding of the role of a regulatory professional
• You demonstrate a learning mentality, are engaged in personal growth, and actively seek and act on feedback
• You foster partnership, collaboration, empowerment, and autonomy to build a strong community

Additional Information

• Department: Global Product Development Regulatory (PDR)
• Hours: full-time (40 hours per week)
• Start date: 1 May 2027
• We have 2 available positions in this recruitment cycle
• The recruitment process will include two rounds of interviews with selected candidates, providing an opportunity for us to get to know you better and for you to demonstrate your suitability for the role

Application

The statements made in this job description are intended to describe the general nature and level of work being performed by those persons assigned to this job. These statements are not intended to be a comprehensive list of all responsibilities, duties and skills required of people assigned to this job.

For this position, relocation is not supported by the employer.

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.