US-NJ, 2018 Internship Program, Global Development Quality Audit Intern 234539BR-MZ
2018 Internship Program, Global Development Quality Audit Intern
Global Drug Development
East Hanover, NJ
USA Novartis Pharmaceuticals Corporation, East Hanover, NJ
You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV.
The Global Development QA Intern will work with the Audit Operations team to assist in the development of the 2019 audit plan and vetting of audit targets. The GDQ Audit Intern will also work on enhancements to the reporting capabilities of the audit tracking database used for operational reporting purposes. The Intern will also assist with other key operational tasks/initiatives to ensure the department meets its objectives and successfully executes the 2018 Unified Quality Audit Plan.
AQWA data clean-up project and data management support
Contribute to the initial planning of the 2019 Unified Quality Audit Plan, including coordination of business / Clinical Quality study feedback and risk assessment/site selection.
Consolidate edits and feedback for required documentation
Provide assistance to operations team in certification management in audit database
Third party audit document requests
Fulfilling ad hoc requests for audit information from Quality and business partners
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.
Key Must Have Competencies/Experiences
Excellent organizational and interpersonal skills; attention to detail
Experience/high learning agility with databases
Basic knowledge of regulations and guidelines for pharmaceutical industry
Intermediate level of skill in the use of Microsoft Access
Trackwise system knowledge a plus
Experience in Quality Assurance and/or Clinical Development a plus
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