AstraZeneca Hiring Executive Regulatory Affairs – M Pharm/B Pharm/MSc

Apply now for Executive Regulatory Affairs at AstraZeneca, Delhi. Openings for M.Pharm/B.Pharm/M.Sc with 2-3 years of regulatory experience. High-growth opportunity.

Executive Regulatory Affairs Opportunity at AstraZeneca – Delhi Location

Looking to advance your career with a top-tier biopharmaceutical company? AstraZeneca India is hiring Executive Regulatory Affairs professionals in Delhi. Candidates with M.Pharm, B.Pharm, or M.Sc qualifications and 2–3 years of experience in India’s regulatory function are encouraged to apply.

Why Join AstraZeneca?

AstraZeneca is a science-led, patient-focused pharmaceutical giant known for innovation in discovering, developing, and commercializing prescription drugs across several major disease areas. The company promotes a culture of collaboration, empowerment, and continuous learning—making it a leading employer in the pharma industry.

Job Role Summary

Key Responsibilities:

• Monitor and promptly report status of all product licenses.
• Implement submission plans for new product approvals and license maintenance.
• Manage SUGAM submissions and regulatory tracker archives.
• Execute timely submissions: test licenses, CT updates, IB amendments, EC approvals.
• Address queries from Health Authorities.
• Provide regulatory support for tenders and clinical trial documents.
• Collaborate across cross-functional teams – Marketing, Medical, QA, Legal, Sales, and Global Product Teams.
• Maintain detailed records of regulatory compliance and submission history.

Compliance & Ethics:

• Follow AZ’s code of conduct, maintain confidentiality and align with audit requirements.
• Ensure proactive tracking and communication of license status and changes.
• Support audits, CAPAs, and clinical research submissions.
• Contribute to artwork review and import license renewals.

Eligibility Criteria

Required Educational Background:

• M.Pharm (Master of Pharmacy)
• B.Pharm (Bachelor of Pharmacy)
• M.Sc (Master of Science – preferably in Life Sciences, Pharmaceutical Sciences, Chemistry)

Experience:

• 2–3 years in Regulatory Affairs within the Indian pharmaceutical industry.
• Knowledge of dossier compilation and Indian regulatory frameworks is essential.

 Job Location

• Delhi, India

 Skills & Competencies

• Strong communication and coordination skills
• Familiarity with Health Authority queries and SUGAM portal
• Dossier management and submission planning
• Cross-functional collaboration
• Proactive project ownership

How to Apply?

Visit the official job page and submit your application here: 👉 Apply Now

 Summary Table