Viatris

Quality Systems Specialist

In short

This role develops and runs site Quality Systems supporting manufacture and release of combination products at a global healthcare manufacturer, covering SOPs, change control, CAPA, internal auditing, vendor qualification and inspection readiness. It requires close collaboration with Engineering, Validation, Manufacturing and Regulatory teams, plus support for regulatory compliance and continuous improvement initiatives. Candidates need a degree, 3+ years of industry experience, and working knowledge of EU & US regulatory requirements, with experience in quality systems, inhalation dosage forms, and systems like Trackwise or SAP being advantageous.

Company
McDermott Laboratories Limited
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.
Key Responsibilities
•Develop and implement site Quality Systems to support the manufacture and release of Combination products, including SOPs, document control, change control, investigations, CAPA, internal auditing, Vendor qualification & management, material and batch disposition, complaints and annual product review.
•Provide QA support to site to ensure Inspection Readiness.
•Collaborate with key stakeholders including Engineering, Validation, Manufacturing, Regulatory and Global Quality.
•Support operation of the site Training system, including preparing and presenting relevant training material, as required.
•Regulatory Compliance; support Dublin Respiratory reviews and generation of supporting documents including API Declaration, Approved Product List, Approved Oversight List.
•Keep abreast of regulatory initiatives and new guidance/requirements.
•Ensure compliance with appropriate regulatory guidance documents, while driving improvements in product and process quality.
•Support the implementation of the Continuous Improvement program by identifying, leading and implementing improvements.
•Comply with company and Legislative Environment, Health and Safety Requirements.
•Support and execute any other duties as assigned.
Minimum Qualifications
•Educated to degree level with 3+ years industry experience.
•Working knowledge of EU & US regulatory requirements.
•Experience in designing and implementing quality systems and/or a start-up an advantage.
•Experience in or knowledge of inhalation dosage forms an advantage.
•High proficiency in Microsoft Word/Excel/PowerPoint/MS Project etc.
•Proficiency in electronic systems/databases such as documentation, Trackwise, SAP etc.
•Good team working and strong communication skills across functions and organization.
•An ability to work flexibly in a changing environment. Good attention to detail and priority management essential.
•Flexibility to learn new skills and take on new tasks and responsibilities.
•The ability to work under pressure to demanding schedules is important, as is the ability to work on one's own initiative.
Benefits
Competitive salaries, benefits and an inclusive environment.

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