What are the responsibilities and job description for the Pharmacovigilance QA Auditor Specialist position at Johnson & Johnson?
Janssen Pharmaceuticals, Inc. a member of the Johnson & Johnson family of companies, is currently recruiting for a Pharmacovigilance QA Auditor Specialist in Raritan, NJ!
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. Janssen Research & Development, LLC is part of the Janssen Pharmaceutical Companies.
Are you interested in joining a team delivering outstanding results to our customers and patients? Apply now for this exciting opportunity!
As a Pharmacovigilance Quality Auditor Specialist you will be part of a dynamic global team working to enhance quality across the Company through pharmacovigilance audit and business partner collaboration.
Key Responsibilities:
- Leads the planning, conduct and reporting of routine PV audits
- Supports non-routine audits of activities, data, internal facilities and processes in GxP/non-regulated areas
- Supports regulatory inspections in various supporting roles.
- Participates in projects or serves on teams, as assigned by supervisor.
- Provides consultation to business partners on routine tasks with occasional supervision.
- Collaborates with business partners when contacted for compliance inquiries and seeks advice on non-routine and more complex issues to ensure a departmental unified position.
- May assist in the preparation of training material if requested.
Salary : $75,000 - $110,000