Novartis Pharmaceuticals

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Novartis Pharmaceuticals currently has the following jobs that match your search criteria.

 
View Job Description Sr. Validation Specialist / Engineer Focus: Computer Systems Validation The Senior Validation Specialist is responsible for planning, scheduling, execution
View Job Description Prepare IQ/OQ/PQ Protocols and Summary Reports for qualification of various engineering projects. Projects include production and research facilities and
View Job Description Supports day to day site compliance needs for the Process Unit. Resolves compliance issues within the Process Unit unilaterally and cross-functionally. This
View Job Description Sr. Validation Specialist / Engineer Focus: Utility/Facility Qualification The Senior Validation Specialist is responsible for planning, scheduling,
View Job Description Sr. Validation Specialist / Engineer Focus: Process Validation The Senior Validation Specialist is responsible for planning, scheduling, execution and
View Job Description Responsible for executing manufacturing process technical support functions for Novartis US Pharm Ops. Performance influences objectives of technology
View Job Description The controls and instrumentation engineer is responsible for leading all controls and instrumentation activities for the roll out of serialization technology
View Job Description The Validation Specialist I and II are responsible for authoring and executing validation project documentation. Validation assignments include validation
View Job Description To manage the Analytical Services team to ensure timely delivery of responsible services and to ensure that all aspects of team activities comply with cGMP
View Job Description Supports day to day site compliance needs for the Process Unit. Resolves compliance issues within the Process Unit unilaterally and cross-functionally. This
View Job Description Supports day to day site compliance needs on the shop floor. Identifies and resolves compliance issues within the Process Unit unilaterally and
View Job Description The Validation Specialist I and II are responsible for authoring and executing validation project documentation. Validation assignments include validation
View Job Description Lead and direct the engineering function's daily activities within Pharmaceutical Operations to ensure the Suffern Site (GMP Manufacturing and Packaging
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