QA Operations Supervisor
viatris · Inverin, County Galway, Ireland · On-site
Posted Oct 6, 2026
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Mylan Teoranta
Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.
We have been included on number of award lists that demonstrate the impact we are making.
Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach, and better access to treatment.
For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.
The Role & What You Will Be Doing
Every day, we rise to the challenge to make a difference, and here’s how the QA Operations Supervisor role will make an impact:
This position will lead the local medical team, ensure alignment and execution of local/regional medical strategy, collaborate with cross-functional teams and influence key healthcare stakeholders to drive meaningful impact for patients and the business.
Conduct checks and reviews of manufacturing operations to ensure GMP compliance and monitor factors which may affect product quality. This includes but not limited to monitoring of Aseptic Practice and techniques during assembly/ machine set up/ filling activities and adherence to procedures. Review handling of interventions for the manufacturing process, and EM monitoring.
Collaborate with manufacturing and engineering functions to drive quality awareness, facilitate Good Manufacturing Practices and implement improvements to ensure product quality.
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Monitor key quality indicators within the manufacturing processes to identify unexpected events and preventative measures in order to ensure continued product quality.
Perform spot checks of logbooks and manufacturing documentation to ensure GDocP compliance.
Assist in facility audits or Health Authority Inspections.
Assist in the delivery of quality related training applicable to your job role and continuous improvement projects.
Support event reporting and investigations applicable to the manufacturing area.
End of shift summary with manager and or Quality director
Perform QA review of executed manufacturing batch records and associated quality control testing (Chemistry and Microbiology). Support processing of…