Regulatory Affairs Associate

Regulatory Affairs Associate - One PDR

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. 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:

• Delivers on projects with mentorship and actively builds foundational regulatory experience with the support of colleagues.

• Owns their learning and development, actively seeking to understand drug development and regulatory roles, and engaging in knowledge sharing and peer support.

• Responsible for understanding and applying business processes to deliver foundational regulatory deliverables.

• Engages with the team through active listening, practicing open communication, and building trust within regulatory and cross-functional teams.

• Grasps the vision of the Roche organization, understanding how their work impacts the team and contributes to overall goals.

• Improves prioritization and time management skills while spending significant time on-site at Roche office.

Who you are:

• You hold a degree (B.Sc., M.Sc., or Doctorate) 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.

• You have a basic understanding of drug development and entry level understanding of the role of a regulatory professional.

• You have no more than 1-year of relevant past pharmaceutical experience.

• Demonstrates a learning mentality, engages in personal growth, and actively seeks and acts on feedback.

• Fosters partnership, collaboration, empowerment, and autonomy to build a strong community.

Submit your application including your Curriculum Vitae and cover letter with responses to the following:

• What is your motivation to join the One PDR Early Talent Program at Roche?

• What technical and personal competencies would you bring along to the One PDR Early Talent Program?

Additional Information:

• Department: Global Product Development Regulatory (PDR).

• Location: Based in South San Francisco, United States.

• Hours: Full-time (40 hours per week).

• Start date: April 2026 or upon agreement.

• Length: 2-year work term

• Number of Positions: 2 available in this recruitment cycle.

Relocation benefits are not offered for this job.

The expected salary range for this position, based on the primary location in California, is $56,800 – $105,600 USD annually. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also includes paid holiday time off benefits.

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.