Regulatory Affairs Postgraduate Program Participant (Male) / Regulatory Affairs Postgraduate Program Participant (Female)

Job ID

REQ-10077016

Date

May 20, 2026

Location

Switzerland

Summary

The Regulatory Affairs Postgraduate Training Program presents a unique opportunity to explore the global functions of Regulatory Affairs and Regulatory Chemistry, Manufacturing and Controls. Successful candidates will engage in a dynamic training position that includes two rotational assignments, each lasting one year, within different Regulatory Affairs functions.

About the Role

Are you eager to delve deeper into Regulatory Affairs (RA) and the pharmaceutical industry?

Following your Master’s or Doctoral qualifications, are you looking to build a career in Regulatory Affairs?

Do you possess a collaborative mindset and take ownership of your tasks? Are you adaptable and skilled at problem-solving while seamlessly integrating with various teams and concepts?

If so, this program offers you the chance to gain vital experience within a cross-functional team in the multicultural and diverse environment of a leading global healthcare company.

Role Responsibilities

Responsibilities may include, but are not limited to:

• Interacting with global interdisciplinary project teams to provide strategic regulatory input for development, submission planning, and necessary documentation, including timelines and strategic risks.
• Supporting and/or preparing high-quality dossiers and documentation related to drug substances and drug products for global regulatory submissions (e.g., Clinical Trial Applications, Market Authorization Applications, post-approval variations, etc.).
• Ensuring adherence to specific requirements in various countries and regions.
• Assisting in submission and response activities, including planning, preparation, review, coordination, and submission.
• Promoting regulatory compliance by raising awareness of requirements and guidelines, facilitating timely submissions of variations, and participating in the change control process.
• Contributing to the development and maintenance of globally consistent product information.
• Supporting the Regulatory Intelligence team by analyzing the EU Regulatory Framework and informing the internal RA community.
• Monitoring, searching for, and evaluating legislation and guidelines from diverse sources.

Duration and Start of Training

The training program lasts for two years, with an anticipated start date in January 2027.

Application Details

Apply online using the form below. Please note that only applications matching the job profile will be considered.

Minimum Requirements

• A strong interest in Regulatory Affairs and Drug Development.
• Completion of an MSc, PhD, or PharmD in Pharmaceutical Sciences, Pharmacy, Life Sciences, or equivalent within the last 24 months.
• Fluency in English (both written and spoken).
• A CV and cover letter in English are required to apply.
• In your cover letter, please clearly articulate your desire to join this particular program, your specific motivations for Regulatory Affairs, and how this opportunity aligns with your future career aspirations.
• An open-minded attitude with an international outlook and a readiness to expand your knowledge.
• Strong interpersonal skills, demonstrating the ability to communicate effectively with individuals from diverse backgrounds and various hierarchical levels, both within and outside the company.

Please note that we can only accept applicants who are eligible to work in Switzerland or have completed their studies at a Swiss University.

Diversity and Inclusion

Novartis is an equal opportunity employer committed to embracing and leveraging diverse backgrounds.

Accessibility and Accommodation

Novartis is dedicated to working with and providing reasonable accommodations to all individuals. If you require accommodations due to a medical condition or disability during the recruitment process, please contact us at diversity.inclusion_ch@novartis.com, and provide details about your request along with your contact information. Kindly include the job requisition number in your message.

Why Novartis

Helping individuals affected by diseases and their families requires more than innovative science; it requires a community of intelligent and passionate people like you. By collaborating, supporting, and inspiring one another, we can achieve breakthroughs that transform patients' lives. Are you ready to create a brighter future together? Learn more about us.

Benefits and Rewards

Explore all the ways we support your personal and professional growth. Read our handbook (PDF 30 MB).

Division

Development

Business Unit

Development

Location

Switzerland

Site

Basel (City)

Company / Legal Entity

C028 (FCRS = CH028) Novartis Pharma AG

Functional Area

Others

Job Type

Full time

Employment Type

Early Career (Fixed Term)

Shift Work

No

Others Development Switzerland

Job ID: REQ-10077016

Regulatory Affairs Postgraduate Program Switzerland

Apply online using the form below.