Team Member- Artwork Team at Dr Reddy's Laboratories Limited

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

21 Sep, 26

Salary

0.0

Posted On

23 Jun, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Artwork Lifecycle Management, Adobe Illustrator, Karomi, Proofreading, Regulatory Compliance, Packaging Development, Change Control Management, Metadata Verification, Cross-functional Coordination, Documentation

Industry

Pharmaceutical Manufacturing

Description

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description 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. Qualifications M. Sc or B.Pharm Additional Information 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/#!/ Job Family: Regulatory Affairs Sub Job Family: Documentation Preferred type of working: On-Premise Years of Experience: 6 - 12 Business unit: EUG

Responsibilities

Manage the artwork lifecycle and support new product launches for the EU region, ensuring high-quality delivery in alignment with regulatory requirements. Coordinate with Regulatory Affairs and cross-functional stakeholders to execute artwork development and updates.