摘要
About the Role
Preferred start date: 01. April 2025
Duration: 12 months
Language requirements: proficient in both German and English
Your key responsibilities will include:
• Correct, efficient and timely execution of Batch Record Review of filled bulk drug product batches (syringes, vials, ampoules) in accordance with cGxP requirements and in compliance with registration
• Approval of Equipment related specifications (ESP)
• Active participation in the achievement of product delivery targets (On Time Batch Approval, Supply Delivery Dates, Batch record right first time, Batch right first time)
• QA Oversight on shopfloor of manufacturing activities (compounding, filling, visual inspection, storage of bulk drug product)
• Provides support in the evaluation and execution of investigations of deviations
Essential requirements:
• Education: Bachelor or Master degree in natural sciences or pharmacy (completed in the past ca. 12 months; no PhD)
• Languages: German: fluent (oral / written); English: very good understanding
• Experience/Professional requirements: not necessarily required but insight into the manufacturing of medicines in the pharmaceutical industry is an advantage
Desirable requirements:
• Ability to work in a team
• Flexibility
• Open communication and engagement
• Knowledge of Good Manufacturing Practice (GMP)
• Knowledge of MS office and SAP
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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