Job Description Summary
The Regulatory Affairs Postgraduate Training Program is an opportunity to discover the global functions of Regulatory Affairs and Regulatory Chemistry, Manufacturing and Controls. Successful candidates will be offered a training position consisting of two rotational assignments, each of 1-year duration, within two different Regulatory Affairs functions.
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Job Description
Are you interested to learn more about Regulatory Affairs (RA) and the pharmaceutical industry?聽
After your Master鈥檚 or Doctoral qualification, do you want a career in Regulatory Affairs?聽
Do you have a collaborative mindset and take ownership of assigned tasks? Are you able to quickly adapt to different teams and concepts, with excellent problem-solving skills?聽
Would you like to work and gain experience in a cross-functional team in the multicultural and diverse environment of a leading global healthcare company?聽
The Regulatory Affairs Postgraduate Training Program is an opportunity to discover the global functions of Regulatory Affairs and Regulatory Chemistry, Manufacturing and Controls.聽
Successful candidates will be offered a training position consisting of two rotational assignments, each of 1-year duration, within two different RA functions.聽
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Responsibilities can include, but are not limited to:聽
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Interacting with global interdisciplinary project teams to provide strategic regulatory input to development, submission planning, documentation needed, as well as timelines and strategic risks聽
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Supporting and/or preparing high quality dossiers, drug substance and/or drug product quality documentation to support global regulatory submissions (e.g. Clinical Trial Applications, Market Authorization Applications, post-approval variations etc.)聽
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Supporting and/or preparing high quality dossiers according to specific requirements in the different countries and regions聽
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Supporting submission and response activities (planning, preparation, review, coordination, submission)聽聽
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Ensuring regulatory compliance by creating awareness of requirements and guidelines, facilitating timely submission of variations and participation in the change control process聽
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Supporting the development and maintenance of globally consistent product information聽
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Supporting the Regulatory Intelligence group analysing the EU Regulatory Framework and informing the internal RA community聽聽
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Monitoring, searching for and evaluating legislation, as well as guidelines from different sources聽
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Duration and start of training: 2 years with an expected start date beginning January 2027聽
Deadline for applications: June 3, 2026聽
Interviews: September 2026聽
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Minimum requirements:聽
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Strong interest in Regulatory Affairs and Drug Development;聽
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Completion of an MSc, PhD or PharmD in Pharmaceutical Sciences/Pharmacy/Life Sciences or equivalent within the last 24 months;聽
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Fluency in English (written and spoken);聽聽
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CV and Cover letter in English required to apply;聽
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For your cover letter, please consider addressing the following:聽Articulate clearly your desire to join this particular program, your specific motivations for Regulatory Affairs and how this opportunity will facilitate your future career ambitions in Regulatory Affairs聽
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Ready to expand your knowledge and are open minded with an international outlook聽
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Strong interpersonal skills i.e. can demonstrate your ability to communicate well with people from a variety of backgrounds/cultures and at different hierarchical levels inside and outside the company聽
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Please note that we can only accept applicants who are eligible to work in Switzerland or have completed their studies at a Swiss University.聽
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Novartis is an equal opportunity employer committed to embracing and leveraging diverse backgrounds.聽
Accessibility and accommodation:
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com, and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
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Skills Desired