Novartis hiring Global Regulatory Submission publishing Associate

Job Description

26 major approvals. 13 major submissions. 2,000 associates worldwide. That was Regulatory Affairs in 2020. We are a culturally diverse, global team of talented professionals seeking to leverage the voices of our patients in our approach to bringing potentially life-changing therapies to people who need them. Novartis has a robust pipeline, including possible treatments for rare disease conditionals with unmet needs.

We are expanding our global team and encourage you to consider a career in Regulatory Affairs at Novartis. Working collaboratively and interactively thanks to our technology, we have been as connected as ever—OneRA as we call it. We pride ourselves on our patient-focused mindset and dedication, which allow us to work closely with colleagues, share knowledge, and strive to reimagine medicine. Read on to learn what you could do as part of our closely knit team.

Your responsibilities include, but are not limited to:

• Responsible for electronically preparing, publishing, quality reviews, validation (using eCTD validator tool), and dispatch activities related to regulatory submissions (e.g., INDs, BLAs/NDAs, MAAs, HA AtoQs, Global Labeling, Annual Reports, etc.).

• Produce high quality, HA compliant submission outputs in varying formats (eCTD, NeeS and Paper) in adherence to assigned timelines and in compliance with worldwide HA requirements (US, EU, LACan, Most of World).

• Partners with Operations Submission Managers and a publishing team located in 3 regions (e.g., US, EU and India) and actively functions in a global capacity.

• Liaises /collaborates with cross functional team members and document authors (e.g., Project Management, Clinical, Nonclinical, CMC, Safety and Quality functions) to achieve timely dispatch of high quality submissions.

• Comply with and actively apply internal work practices and guidelines.

• Support implementation of new technologies, tools and processes as well as contribute to ongoing initiatives and training efforts.

• Identify process or technical issues and propose solutions relating to timing, quality, compliance and resources.

• Contributes to process efficiencies, process documentation and knowledge transfer efforts within the RA team.

Minimum requirements

• 3-5 years submission publishing experience in Pharma or related industry.

• Experience with regulatory submission format, including familiarity with submission publishing activities and CTD format criteria.

• Effective interpersonal skills, strong written and oral communication and presentation skills. Project management and time management skills to manage multiple ongoing projects simultaneously.

• Familiar with regulatory requirements and HA guidances, including FDA regulations, ICH and EMA guidelines/directives.

• Working knowledge of regulatory affairs. Works independently and with minimal supervision.

•Proficiency with computer programs/systems (MS office, etc.) with demonstrated ability to learn new systems quickly.

• Analytical skills and problem solving skills. Ability to coordinate and work effectively with cross-functional teams.

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