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/MSc 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 MSc 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)
• MSc (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

Company Name	Current Vacancies in Departments	Required Education	Experience Required
AstraZeneca India	Regulatory Affairs	M.Pharm, B Pharm, MSc	2–3 Years