To release product that meets required quality and manufactured standards to affiliates and the public.
Ensure that products are manufactured to appropriate cGMP standards by reviewing all deviations related to all processes within operations, including compounding, filling, packaging and product release.
Act as lead trainer for new QA associates.
Provide guidance to production and maintenance groups on intervention recovery methods in the aseptic areas.
Review critical alarms assessments and assist with investigations as necessary.
Author, review and approve QA documents and procedures.
Assist in smoke studies, media program and other validation/compliance activities in the aseptic areas.
Review and approve sterility break request forms.
Submit quality data metrics requested by Global, such as cockpit.
Right first time
MNCs associated with QA error
On-time training completion Safety suggestions/input Continuous Improvement suggestions/input
The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
Minimum Education: BS in Science or Engineering with 3 years experience Preferred Education: Advanced degree in Science or Engineering, ASQ Certified Quality Engineer with 5 years experience. English Minimum Education: BS in Science or Engineering with 3 years experience Preferred Education: Advanced degree in Science or Engineering, ASQ Certified Quality Engineer with 5 years experience.
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