Cmc Regulatory Affairs Manager
hace 2 semanas
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.
Our Chemistry, Manufacturing, and Controls (CMC) Regulatory function spans across the product lifecycle and is responsible for the regulatory strategy relating to the development, manufacture, and testing of all our medicines. With our expertise, we interpret, anticipate, and shape global Health Authority expectations to build insightful CMC and Device Regulatory Strategies.
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 lifecycle. 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.
**Accountabilities**:
- 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 are shared with other colleagues/within the functions.
- Participation in regulatory execution and delivery meetings and communicate and provide relevant updates to the international CMC team.
- Contribute to business process optimisation activities to reduce waste and ensure efficiency.
- Continually evolve and develop the regulatory expertise through proactive recording and communications of Health Authority interactions, responses, and commitments.
**Essential Skills/Experience**:
- Bachelors 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
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Be empowered with the tools to innovate This is a place for innovation and originality. Empowered to take smart risks with the tools of a leading pharmaceutical fused with an agile mindset. It means we are encouraged to be fearless and break barriers to develop better solutions. It's through our creative ideas that we uncover innovative regulatory approaches and pathways.
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