Require Manager Regulatory Affairs at Boehringer Ingelheim

Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry’s top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain.

Post : Manager Regulatory Affairs

The Position
Ensure that all regulatory updates are shared with local and global teams in timely manner. Ensure that timely and complete regulatory actions are taken regarding assigned product/therapeutic area. Ensure operational RA tasks are executed in timely manner

Duties & Responsibilities
• Registration of NCE and line extensions for therapeutic area of responsibility
• Strategies compliant with regulations, Liaise with Health Authority and ensure earliest submission and registration in the country.
• Follow-up regulatory approvals for the products per registration plan.
• Liaise with Health Authority regularly and engage in impactful discussion with Senior Regulatory officials.
• Ensure earliest submission & approvals at the right time to ensure quick implementation of proposed CMC changes as per global timelines.
• Renewal on time to ensure uninterrupted availability of products in the country.
• Amendments and updates are approved on time to ensure study is continued in the country and ensure timely notification of notifiable updates.
• Follow-up on submitted applications at HA.
• Regulatory Intelligence, ensure all regulatory updates are shared with local and global team in timely manner. Follow the RI procedure of making entry and impact assessment of each relevant update in RINTOOL to maintain RIN database.

Candidate Profile
• Education: Bachelor’s degree in pharmacy or similar medical education.
• Pharma experience with regulatory focus in a multi-national for at least 8-10 years.
• Proven track record of Strong Liaising experience in the health authority
• Solid understanding of D&C Act and Rules.
• Understanding of working practices at HA.
• Experience of direct interactions with Regulatory Authorities.
• Eye for details
• Analytical skills
• Communication skills
• Negotiation skills
• Position is based in Delhi

Additional Information
Experience : 5+ years
Qualification : B.Pharm
Location : Delhi, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 30th September 2026