JB - 1704 - Regulatory Affairs - Executive Designer

Design and format regulatory documents, product labels, artworks, leaflets, and packaging materials as per approved specifications. Create and modify regulatory artwork using CorelDRAW and other relevant graphic design software. Ensure all artwork and regulatory materials comply with approved text, product specifications, and regulatory requirements. Prepare artwork for product registration, renewals, variations, and regulatory submissions. Coordinate with Regulatory Affairs, QA, QC, R&D, and Marketing teams for artwork development and approval. Review artwork for text accuracy, dimensions, fonts, colors, symbols, barcodes, batch details, and other regulatory information. Make revisions based on regulatory comments, internal review, and country-specific requirements. Maintain proper version control, artwork records, and approved master files. Prepare high-quality print-ready files and coordinate with printing/packaging vendors when required. Ensure timely completion of artwork and documentation while maintaining accuracy and consistency across product materials. Requirements2–5 years of experience in graphic designing, preferably in Pharmaceutical/Healthcare/FMCG regulatory artwork. Strong hands-on expertise in CorelDRAW. Knowledge of Adobe Illustrator and Photoshop will be an added advantage. Understanding of pharmaceutical labels, cartons, foils, leaflets, packaging materials, and regulatory artwork. Basic understanding of Regulatory Affairs and country-specific labeling requirements. Benefits

• Option to work from home or from office depending on operational requirements.
• Exposure to regulatory operations and pharmaceutical product submission processes across multiple markets.
• Opportunity to work closely with manufacturing, analytical laboratories, and regulatory teams.