Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity.
Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.
Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.
About the role
This role will lead the Quality compliance to the new facility, Perform the risk assessment. Review QMS related documents and will be responsible for setting QMS for the recent facility.
Role Responsibilities
Project Start up Phase:
Timely input to the facility/ process/ equipment’s/ logistics quality requirements.
Ensures that appropriate systems are implemented and maintained
influences operational and production facility GMP design, supplier management and site strategy.
Ensures the right validation protocols are developed for the new site validation and documentation.
Regulatory Standards Matching and Mapping
Preparing Validation Master Plan for Site
QMS Documents ( SOP/NCR/ Investigations) Process Set Up
QA SOP and documents drafting
Change Control process Set for Manufacturing Site
Coordination for ISO Audit QMS Documents
Risk Assessments as Per ICH guidelines
Once the site is operational: Commercial production
Ensures that all aspects of the site Quality and Manufacturing tasks comply with the Haleon Quality Manual and meet all relevant cGMP and regulatory requirements.
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