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.
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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
