Assistant Manager-Regulatory Affairs (Artwork & Packaging) Full Time NEW

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies.

Position purpose

• Artwork Management (all components) Understanding and operational efficiency of artwork management system.
• Artwork requests to be raised with India specific annotations.
• Comments received from overseas sites to be addressed and post peer review, approve final artwork files as per artwork approval checklist. Coordination with packaging coordinator, supply chain, BU/ Pricing / Legal team wherever required.
• Support for QR code / serialization implementation as per business and regulatory needs.
• Review and impact assessment of new India regulations relevant to labels if any. Ensure implementation as per timelines in coordination with local/ global stakeholders.
• Support artwork developed for local partners as applicable.
• Support labels of neighbouring markets e.g. Nepal as needed.
• Prepare for audit of labeling activity if any and implement CAPAs if applicable.
• Liaison closely with overseas manufacturing site for labels of 1st launch batch, exploring innovative options for early launch.
• Ensure 100% adherence to internal and external labelling requirements.

Internal customers

Marketing, Logistics, Medical, Legal Affairs Intellectual Property, Global Product Teams (GPTs), Key Brand Teams (KBTs), International Regulatory Affairs (IRA), Manufacturing Sites and QA

External customers Local Health Authorities and other Government Agencies

Minimum requirements Qualification: B. Pharm/ M. Sc 3-6 yrs Experience in India Artwork requirement and knowledge of D&C act for Artwork checklist. Should be conversant with Indian regulations in Artwork development.

Key Result Areas/ outputs

Adherence to AZ and industry codes of conduct, ethics and good regulatory practices

Ensure that all artwork request for assigned products is complete in accordance with relevant norms

Develop and implement action for Artwork development for allocated products to achieve requisite approvals rapidly and facilitate the rapid implementation

• Evaluates impact of new artwork guidelines in liaison with RA leadership

Align with the values and vision of AZ

Ensure compliance with Local legislation, Global regulatory policies, AZ code of conduct, Corporate Governance and Audit requirement

• Ensure that company confidentiality is maintained (i.e. intellectual property, product information and strategic information). Disclose potential breaches of codes or conducts

Ensure that all artwork request for assigned products is complete in accordance with relevant norms.

Monitor status of all product artwork request

• Manage revision in product artworks and coordinate with other changes, planned and in progress
• Maintain complete documentation records and all trackers timely maintained

Develop and implement Action for Artwork development for allocated products to achieve requisite approvals rapidly and facilitate the rapid implementation.

Maintain detailed knowledge of critical aspects of products: commercial strategies, the content of the dossiers, , regulatory timelines and supply strategy and proactive preparation of required steps

• Implement artwork development plan for new launches in conjunction with key stakeholders and deliver plans on time. Track status and take prompt corrective measures whenever necessary to ensure rapid approval of artwork.

Team player, collaboration

• Collaborates with cross functional teams- Supply chain, QA, medical, access as needed and with regional/ international RA colleagues
• Good team player
• Demonstrates ownership and accountability of assigned project with independent handling of projects with minimum supervision from manager/ lead.

Regulatory Compliance and life cycle maintenance

• Ensure timely development and approvals of artwork along with compliances as per external and internal norms with minimum supervision from manager and internal databases
• Support relevant audits internal and external
• Supports deviations/ CAPA as needed for artwork deviations

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare.

You can find alternative messaging to use in the ‘Global Talent Attraction Story messaging’ section of the Global Playbook on the Employer Brand Portal – try to use other examples in order to make it different for candidates!

So, what’s next?

• Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.
• Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours.

Where can I find out more?

Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/

Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/

Date Posted

08-May-2026

Closing Date

21-May-2026

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.