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Rhydburg Biotech

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JB - 1704 - Graphic Designer

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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.



Skills

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See also

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