JB - 1704 - Graphic Designer
Summary
Designs and formats regulatory pharmaceutical artwork — product labels, leaflets, cartons, foils, and packaging — primarily in CorelDRAW (Adobe Illustrator/Photoshop a plus), ensuring compliance with approved text and country-specific regulatory requirements while coordinating with Regulatory Affairs, QA/QC, R&D, and print vendors.
- 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.
Requirements
- 2–5 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.