"Unlock Your Career Potential as an International CMC Regulatory Affairs Manager at AstraZeneca!"
"Unlock Your Career Potential as an International CMC Regulatory Affairs Manager at AstraZeneca!"

AstraZeneca BPharma Jobs – Apply For International CMC Regulatory Affairs Manager

International CMC Regulatory Affairs Manager

Type: Full time

Posted: Today

Job Requisition ID: R-184660

Location: India – Bangalore

Job Description

About AstraZeneca

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.

Chemistry, Manufacturing, and Controls (CMC)

Our Chemistry, Manufacturing, and Controls (CMC) Regulatory function spans across the product lifecycle and are responsible for the regulatory strategy relating to the development, manufacture, and testing of all of our medicines.

With our expertise, we interpret, anticipate and shape global Health Authority expectations to build insightful CMC and Device Regulatory Strategies.

What you will do:

The role holders effectively manage the delivery, compilation and production of Chemistry, Manufacturing and Control (CMC) documentation for designated product ranges to deliver the needs for the international region and filings according to accelerated wave plans. They project manage global CMC regulatory submissions ensuring that project activities and documentation are delivered

to the required standards across the product Lifecyle. The role holder will contribute and lead the regulatory CMC components of business-related projects. They will have effective levels of interactive communication with stakeholders and project team members to ensure relevant timelines and regulatory commitments are communicated.

They will ensure the application of international CMC regulations and guidance within AstraZeneca and lead/contribute to the development of new guidance, policy, and processes.

Key Responsibilities:

  • Manage the timely preparation (may include authoring) and delivery of CMC contributions to the regulatory submissions linked to medicinal products throughout the lifecycle; including marketing authorisation applications and all post-approval activities.
  • Accountable for delivering “submission ready” international CMC modules to internal and external regulatory stakeholders in compliance with relevant AstraZeneca systems and procedures and ensuring submission quality.
  • Documenting maintenance and communication of Health Authority approval status.
  • Develops and builds expertise in regional regulatory requirements to ensure assurance of compliance of CMC submissions.
  • Project management expertise with the ability to adapt to changing situations to ensure on-time delivery.
  • Ensure the learning from own projects is shared with other colleagues/within the functions.
  • Supporting the agreed strategy to employ fit for purpose content applying regulatory intelligence and to optimize proposed submission content.
  • Participation in regulatory execution and delivery meetings and communicate and provide relevant updates to the international CMC team.
  • Contribute to business process optimization activities to reduce waste and ensure efficiency.
  • Continually evolve and develop regulatory expertise through proactive recording and communications of Health Authority interactions, responses, and commitments.
  • Apply GxP principles according to the stage of the product lifecycle.

Essential Requirements

  • Bachelor’s degree in Science, Regulatory Sciences, or Pharmacy.
  • Experience in Regulatory / Drug development (Industry or Health Authority).
  • Breadth of knowledge of manufacturing, project, technical, and regulatory management.
  • IT Skills.
  • Stakeholder & Project management.

Professional capabilities: Regulatory knowledge

APPLY ONLINE HERE

Keywords: International CMC Regulatory Affairs Manager, AstraZeneca, Chemistry, Manufacturing, and Controls, Regulatory strategy, Drug development, Project management, Compliance, GxP principles. AstraZeneca BPharma Jobs – Apply For International CMC Regulatory Affairs Manager. Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.

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