Glenmark Pharma Hiring: Officer – Labelling Regulatory Operations

Are you passionate about regulatory affairs and global labelling compliance?
Here’s your chance to join Glenmark Pharmaceuticals, a global innovation-driven pharmaceutical company, as an Officer – Labelling Regulatory Operations within the Global Regulatory Affairs (GRA) team.

This position offers a dynamic platform to work on labelling management, safety assessments, and compliance documentation for multiple global markets — including the EU, USA, Canada, Australia, and New Zealand.

If you have a background in pharmaceutical sciences and experience in labelling operations, this role is your gateway to a rewarding regulatory career.

Key Responsibilities

• Manage labelling and safety assessments for global products
• Review and maintain Reference Safety Information (RSI) for Glenmark products
• Author and review Labelling Core Notification Forms (LCNF), Summary of Product Characteristics (SmPC), and Patient Information Leaflets (PIL) for the EU region
• Maintain trackers for labelling updates and safety documentation
• Collaborate with cross-functional teams to ensure timely regulatory submissions
• Exposure to labelling requirements across the USA, Canada, Australia, and New Zealand will be advantageous
• Familiarity with RIMS and eCTD systems is desirable

Qualifications and Experience

• Qualification: B.Pharm / M.Pharm
• Experience: 1 to 3 years in labelling or regulatory operations
• Strong understanding of pharmaceutical regulations, product safety, and documentation workflows

Benefits of Working at Glenmark

• Opportunity to work in a globally recognized pharmaceutical company
• Exposure to multiple regulatory markets
• Professional growth in a collaborative environment
• Competitive compensation and employee benefits
• Learn from seasoned regulatory experts and innovators

How to Apply

Interested and eligible candidates can send their updated resumes to:
📩 purna.ambekar@glenmarkpharma.com