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Job Description
Career Level: D
Introduction to role:
Are you ready to lead the charge in transforming drug development strategies into reality As a Regulatory Affairs Manager II, youll be at the forefront of coordinating, developing, and implementing new and revised printed labeling for our commercial products. Your expertise will ensure that packaging components meet regulatory standards across the US, export markets, and EU centralized procedures. Dive into a role where your strategic input and leadership in cross-functional activities will drive continuous improvement in processes and tools.
Accountabilities:
What youll do:
- Ensure all work is performed in accordance with established procedures, regulatory requirements, and GxPs.
- Serve as the point of contact for managing all labeling/artwork requests for allocated products requiring market/regulatory approval in the US, markets receiving a standard export pack, and EU centralized procedures.
- Coordinate and/or lead the development and lifetime maintenance of packaging component labeling for commercial products, including new pack introductions, product launches, updates to existing packs, and mock-ups for regulatory submissions.
- Collaborate with marketing company colleagues regarding global artworks as appropriate.
- Engage with operations/manufacturing sites regarding implementation of global artworks as needed.
- Ensure proper version control and document integrity of packaging component labeling, printed labeling artworks, and other assigned labeling documents.
- Process and prepare all final printed labeling for the US and required EU specimens for submission.
- Relevant university degree in science or related discipline
- Minimum 7 years of regulatory experience within the biopharmaceutical industry, preferably working with labeling
- Keen attention to detail and accuracy
- Thorough knowledge of labeling regulations and guidance
- Strong project management skills
- Leadership skills, including experience leading multi-disciplinary project teams
- Experience in packaging labeling development and/or maintenance
- Experience working with stakeholders from locations outside of India, especially Europe and/or USA
At AstraZeneca, innovation drives us forward. We are committed to pushing beyond traditional regulatory approaches to develop progressive solutions that prevent and treat diseases. Our diverse team thrives on curiosity and collaboration, empowering us to make quick decisions and influence drug development strategies. With a focus on technology adoption and automation, we strive for efficiencies that bring life-changing medicines to patients faster. Here, youll find a supportive environment where your professional growth is nurtured through our Regulatory academy and development path.
Ready to make an impact Apply now to join our dynamic team and be part of shaping the future of medicine!
Skills
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About Company
Important dates & deadlines?
Application Deadline
04 Jul 25, 03:29 PM IST
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