Summary
About the Role
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.
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