Internship Manufacturing
Summary
Support Manufacturing unit where sterile products are assembled and packaged. After familiarization with our procedures and processes you will provide front line technical and scientific support for process-specific issues to ensure execution of processes on-time and in compliance to Good Manufacturing Practice.
About the Role
Major accountabilities:
• Contact person for products and process problems that arise during the ongoing process• Collaboration in the preparation of Standard Operational Procedures for routine processes and inputs for electronic master batch record documentation,• Lead thorough Root Cause Investigation Process using investigation tools and methodology• Application of deviation, complaints, and the implementation of effective corrective actions• Team player with strong team spirit
Key performance indicators:
• Compliance/Quality related KPI's• Customer Complaints• Batch Success Rate
Work Experience:
• work expirience in a GMP environment desirable.
Skills:
• Master degree in Pharmacy , Pharmaceutical Technology, Chemistry or equivalent , also Postgraduate with 1-2 years experience desirable
Languages :
• Advanced English and proficient in site local language
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives.
Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Support Manufacturing unit where sterile products are assembled and packaged. After familiarization with our procedures and processes you will provide front line technical and scientific support for process-specific issues to ensure execution of processes on-time and in compliance to Good Manufacturing Practice.
About the Role
Major accountabilities:
• Contact person for products and process problems that arise during the ongoing process• Collaboration in the preparation of Standard Operational Procedures for routine processes and inputs for electronic master batch record documentation,• Lead thorough Root Cause Investigation Process using investigation tools and methodology• Application of deviation, complaints, and the implementation of effective corrective actions• Team player with strong team spirit
Key performance indicators:
• Compliance/Quality related KPI's• Customer Complaints• Batch Success Rate
Work Experience:
• work expirience in a GMP environment desirable.
Skills:
• Master degree in Pharmacy , Pharmaceutical Technology, Chemistry or equivalent , also Postgraduate with 1-2 years experience desirable
Languages :
• Advanced English and proficient in site local language
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives.
Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
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