Preferred start date: as soon as possible
Latest start date: flexible
Duration: 12 months

Language requirements: proficient in both German and English

Your key responsibilities will include: 

•    Support in the managing technical complaints by driving the manufacturing investigation, supporting Site’s Subject Matter Experts and definition of precautionary measures
•    Support continuous improvement of our activities, procedures and knowledge as well as experience sharing inside and outside the Manufacturing Site
•    Support the preparation of Health Authority responses
•    Administration of and communication with our stakeholders outside Novartis
•    Administration of product samples delivered back from the customers for technical investigation

You will be part of a supportive, open-minded team who is working closely together whilst having independent activities.

Essential requirements:
•    Education: Bachelor or Master graduate in Pharmacy, Chemistry, Microbiology, Biotechnology or another related science (graduation in the past ca. 12 months)

 •    High interest in Quality field
 •    Languages: Fluent German (spoken and written), Business-level English (spoken and written)

Desirable requirements:
•    Initial experience with working in a pharmaceutical company is a plus

Please submit a cover letter that includes your motivation for the position and from when you will be available. Thank you.

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.