An individual contributor position in GDD Regulatory Affairs Operations accountable for all publishing, verification, coordination and dispatch of HA compliant, worldwide regulatory submissions in support of Novartis global product portfolio. The Global Regulatory Submission Publishing Associate will Create, assemble and publish electronic submissions per regulatory requirements with a focus on maintenance submissions worldwide (variations, Response to List of Questions etc.), coordinate internal publishing activities and liaise with cross functional teams and document authors to assist with timelines and deliverables related to submission documents.
Regulatory Submission Publisher
Global Pharma company
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Bachelor’s Degree in life sciences
As per Industry
Candidate should be from relevant discipline with 3-5 years of professional work experience in Pharma or related industry. Familiarity with regulatory requirements and good knowledge on regulatory submission format, particularly CTD/eCTD is must. Proficiency with MS office and publishing software (e.g. eCTDXpress, DocuBridge, etc.) is required.
Deutsch: Von Vorteil
Englisch: Sehr gut
If you are interested then kindly send your resume to: firstname.lastname@example.org