Your accountabilities will include:

• Perform QC related investigations like OOS, OOE, OOT or Deviations including report writing
• Perform Deviation reports linked to equipment failures or malfunction
• Define Corrective Actions or Preventive Actions as part of the investigation performed
• Guide analysts during the routine analysis and support in finding solutions in case or problem detection
• Support the senior QC specialist during health authority inspections
• Support KPI tracking and trending
• Generate and review standard operating procedures

What you'll bring to the role:

• Education: bachelor/master degree or PhD in chemistry, bio-chemistry, biology or pharmacy (completed in the past ca. 12 months)
• Laboratory experience
• Resilient and good team player
• Sound technical & scientific knowledge of pharmaceutical/ chemical analytics/QC/ equivalent
• Languages: business-level German and English

Important information:

Application deadline: October 6 EOB. We welcome your application as soon as possible: in the event that we identify suitable candidates sooner, we reserve the right to close the vacancy ahead of the scheduled closing date.

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

Please note that we can only accept applicants who are eligible to work in Switzerland.

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.