Team Member- Artwork Team

The Artwork Officer will be responsible for managing artwork lifecycle activities and supporting new product launches and life cycle management across the EU region. The role involves ensuring timely delivery of high-quality artwork in alignment with regulatory requirements, launch timelines, and implementation schedules.

The incumbent will provide administrative and operational support to the EU Artwork team, while working closely with Regulatory Affairs and cross-functional stakeholders to ensure compliance and seamless execution of artwork development and updates.

Key Responsibilities

Collaborate within the EU Artwork team and coordinate with suppliers, third parties, and cross-functional teams to ensure adherence to artwork timelines and delivery milestones.
Partner with Regulatory Affairs and key stakeholders to contribute to artwork development strategies aligned with implementation and submission timelines.
Develop and deliver high-quality EU artworks using Illustrator and Karomi etc.
Create and maintain cutter asset libraries, including standardized naming conventions and symbol libraries for broader business use.
Support the management and continuous improvement of the artwork management system, ensuring timely completion and accuracy of all artwork deliverables.
Address internal and external artwork-related queries, ensuring efficient communication and timely sharing of required files and information.
Liaise closely with packaging development teams to ensure alignment between artwork and packaging specifications.
Perform detailed proofreading of artwork components against approved briefs to ensure full compliance with applicable regulatory and international guidelines.
Verify accuracy of metadata, including EAN and pharmaceutical codes, ensuring correct orientation and readability.
Coordinate product-related artwork changes in line with regulatory requirements and supply chain plans.
Initiate and manage artwork change controls, including tracking implementation through completion.
Prepare and compile documentation for submission to the Patient Information Quality (PIQ) unit, supporting regulatory notifications and assessment processes.

M. Sc or B.Pharm

About the Department

This role will be part of GG-Europe & will be based out of Bachupally, Hyderabad, India.

Benefits Offered
At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.

Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
For more details, please visit our career website at https://careers.drreddys.com/#!/