AstraZeneca Hiring Regulatory Affairs Executive - M.Pharm, B.Pharm, MSc Apply

AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.

Post : Executive Regulatory Affairs

Job Description
• Monitor and promptly report the status of all product licenses
• Support team in implement submission plan for new products and products maintenance (license, amendments to update registration files etc.) as approved and deliver plans on time
• Manage SUGAM submissions as and when assigned
• Collates, communicates and prepares for Health authorities’ queries
• Maintenance of all Regulatory trackers and archival
• Plan, execute & ensure timely submission of various applications when assigned including but not limited to only these: test license application, HAQ response submission, CT updates and notification submission e.g. IB amendment, site closure, site addition, EC approval submission etc.
• Support tender requirement.
• Align with the values and vision of AZ.
• Ensure compliance with Local legislation, Global regulatory policies, AZ code of conduct, Corporate Governance and Audit requirement.
• Ensure that company confidentiality is maintained (i.e. intellectual property, product information and strategic information).
• Disclose potential breaches of codes or conducts.
• Monitor status of product licenses.
• Project manage changes in product licenses and coordinate with other changes, planned and in progress.
• Maintain complete documentation records and all trackers timely maintained
• Communicate changes to licenses status promptly.

• Maintain detailed knowledge of critical aspects of products: commercial strategies, the content of the dossiers, regulatory intelligence, regulatory timelines and supply strategy and proactive preparation of required steps, manages local testing and legal documents for new launches
• Implement regulatory strategy plan for new launches in conjunction with key stakeholders and deliver plans on time
• Track status and take prompt corrective measures whenever necessary to ensure rapid approval and launch
• Collaborates with cross functional teams- Supply chain, QA, Clinical operations, medical, access as needed and with regional/ international RA colleagues.
• Demonstrates ownership and accountability of assigned project with independent handling of projects with minimum supervision from manager/ lead
• Provide guidance/ training to junior new joiners/ contract associates.
• Ensure timely submission for regulatory compliances for commercial and clinical trials as per external and internal norms with minimum supervision from manager and internal databases
• Support relevant audits internal and external
• Supports deviations/ CAPA as needed
• Ensures timely submission of import registration/ renewal and production transfer to ensure business continuity
• Supports artworks review and local FDA licenses as assigned
• Handles submission/ review/ query responses for global clinical trials/ phase IV/ PMS studies including SEC preparation
• Manages regulatory compliance during study conduct including renewal/ amendments and till study closure with minimum supervision from manager
• Monitor the global pipelines of competing pharmaceutical companies
• Analyse gathered the information for its impact on AstraZeneca’s proposed pipelines as assigned.

Candidate Profile
M.Pharm / B.Pharm / M.Sc 2-3 yrs Experience in India Regulatory function, knowledge of dossier compilation. He/ she should be conversant with Indian regulations.

Additional Information
Experience : 2-3 yrs
Qualification : M.Pharm / B.Pharm / M.Sc
Location : Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 25th May 2025