One Product Development Regulatory (PDR) Early Talent (ET) Program (Basel, 2 years)
Roche is hiring a One Product Development Regulatory (PDR) Early Talent (ET) Program (Basel, 2 years) (Switzerland). Level rates it ; you can apply on Level.
Level's read on this job
- Little AI ●○○○ is how Level rates this role: aI is not part of the work.
- The posting mentions regulatory affairs, pharmaceutical development and scientific writing among its tools and skills.
- Level classes it as an internship.
- Roche has 1,200+ other open roles on Level.
- This posting went up within the past two weeks.
AI in this role
Participate in a two-year early talent program focusing on pharmaceutical regulatory affairs, drug development lifecycles, and 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.
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. By joining the One PDR ET Program, participants become pivotal contributors to the regulatory landscape, dedicated to ensuring that life-changing medicines reach those who need them most.
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
Submit your application including your Curriculum Vitae and motivation letter with responses to the following:
What is your motivation to join the One PDR Early Talent Program at Roche?
Why are you interested in Regulatory Affairs and what technical and personal competencies would you bring to the role?
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.
Ready to take the next step? We'd love to hear from you. Apply now to explore this exciting opportunity!
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.
How we rate this
One Product Development Regulatory (PDR) Early Talent (ET) Program (Basel, 2 years) at Roche rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where regulatory affairs was part of your work. What did you do?
- Tell me about a project where pharmaceutical development was part of your work. What did you do?
- Tell me about a project where scientific writing was part of your work. What did you do?
- Tell me about a project where clinical trials was part of your work. What did you do?
- Tell me about a project where compliance was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Regulatory Affairs, Pharmaceutical Development, Scientific Writing, Clinical Trials, and Compliance. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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