AstraZeneca Regulatory Affairs Jobs For Pharma, Apply Online
Assistant Manager – Regulatory Affairs
India – Bangalore
time type: Full time
posted on: Posted Yesterday
time left to apply: End Date: February 28, 2025 (30+ days left to apply)
Job requisition id: R-217891
About AstraZeneca
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies.
Position purpose
- Monitor and promptly report the status of all product licenses.
- Implement submission plan for new products and products maintenance (license, amendments to update registration files, etc.) as approved and deliver plans on time.
- Collate, communicate, and prepare for Health Authorities’ queries.
- Perform archival and update submission trackers.
Internal customers:
Marketing, Sales, Logistics, Medical, Legal Affairs, Intellectual Property, Clinical Operations, Global Product Teams (GPTs), Key Brand Teams (KBTs), International Regulatory Affairs (IRA), Manufacturing Sites and QA, Regional Office.
External customers:
CDSCO Office, NIB, IPC, CDTL, CDL, NCB & DCK, and other Local Health Authorities and Government Agencies.
Minimum requirements:
- M.Pharm/B.Pharm/ M.Sc.
- 3-6 years of experience in India Regulatory function, knowledge of dossier compilation.
- He/she should be conversant with Indian regulations.
Key Result Areas/Outputs
- Adherence to AZ and industry codes of conduct, ethics, and good regulatory practices.
- Ensure that all licensing for assigned products is complete in accordance with relevant norms.
- Develop and implement action regulatory plans for allocated new products to achieve requisite approvals rapidly and facilitate the rapid launch.
- Evaluate the impact of new guidelines in liaison with RA leadership.
- Support Regulatory competitive intelligence and analysis.
- 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 trackers, ensuring they are updated timely.
- Communicate changes to license status promptly.
- Maintain detailed knowledge of critical aspects of products: commercial strategies, content of dossiers, regulatory intelligence, regulatory timelines, and supply strategy. Proactively prepare required steps, manage local testing, and legal documents for new launches.
- Implement regulatory strategy plans 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.
- 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, both internal and external.
- Support deviations/CAPA as needed.
- Ensure timely submission of import registration/renewal and production transfer to ensure business continuity.
- Support artwork reviews and local FDA licenses as assigned.
- Handle submission/review/query responses for global clinical trials/Phase IV/PMS studies, including SEC preparation.
- Manage regulatory compliance during study conduct, including renewal/amendments and until study closure, with minimum supervision from manager.
Why AstraZeneca?
At AstraZeneca, we’re dedicated to being a Great Place to Work. You are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference in medicine, patients, and society. An inclusive culture champions diversity and collaboration, always committed to lifelong learning, growth, and development. We’re on an exciting journey to pioneer the future of healthcare.
Date Posted: 22-Jan-2025
Closing Date: 27-Feb-2025
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