
Quality Control Analyst
- Baldoyle, Co Dublin
- Permanent
- Full-time
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership – Leveraging our collective expertise to connect people to products and services.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 worldThe Role & What You Will Be DoingEvery day, we rise to the challenge to make a difference and here’s how the Quality Control Analyst role will make an impact:
- 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.
- Educated to degree level with proven experience in the industry.
- 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.