- Equipment Operator - Execute assigned manufacturing tasks and activities according to the production schedule to enable the timely production of products with the required quality and quantity, in compliance with relevant GMP, safety, and environmental guidelines.
- Service Operator - Execute assigned manufacturing tasks and activities according to the production schedule, ensuring compliance with GMP, safety, and environmental guidelines. Perform routine operational support activities to facilitate timely production.
- Documentation Specialist Admin - Manage the modification, editing, distribution, review, and archiving of GMP manufacturing documents, including editing batch records to ensure timely delivery to production. Ensure administrative tasks are performed to support the proper functioning of the unit.
About the Role
Major accountabilities:
* Participation in manufacturing processes.
* Execution of all assigned activities according to the production schedule and in compliance with GMP, work, operating, environmental, and safety instructions and guidelines.
Key performance indicators:
* Deadlines: adherence to production planning and timely task execution.
* Quality: accuracy and error rate in production documents and batch records.
* Time management on the shop floor.
Skills:
* Transportation
* General HSE knowledge
* GMP knowledge
* Transportation classification expertise (e.g., IATA, DOT)
* Manufacturing process execution
Languages :
* German
Why Novartis: Helping people with disease and their families requires more than innovative science. It takes a community of passionate, collaborative individuals like you to achieve breakthroughs that change lives. Join us to create a brighter future: https://www.novartis.com/about/strategy/people-and-culture
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Functional Area: Technical Operations
Job Type: Full-time
Employment Type: Temporary (Fixed Term)
Shift Work: No
Novartis is committed to fostering an inclusive, diverse work environment that reflects the communities we serve.
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