Viatris Jobs in Ireland

The EHS Associate Manager will be responsible for managing the environmental health and safety agenda for the Viatris Northern Cross Global Device Development Group & Office Location. · ...

The role of QC Analyst – Micro involves analyzing raw materials, in-process and finished products. It also includes facility monitoring, reading and trending analytical data, and authorizing reports.Key responsibilities include executing method transfers, compendia verification o ...

We're looking for a Project Manager to support our rebranding efforts globally. You'll be working with multiple teams across different regions to analyze inputs, issue reports and presentations that support decision making. · ...

We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment. · ...

We are looking for a Principal Device Technical Regulatory Specialist to join our Global Device Development organisation. · Subject Matter Expert (SME) in the application of FDA, EU and ISO standards, regulations and guidance related to design control and regulatory compliance: · ...

The Project Manager for rebranding is accountable for all required rebranding and LENC/c activities. · We are looking for a candidate who has an effective combination of project management experience in a multi-national environment.Supporting the Head, Strategic Commercial Transf ...

Provide technical support for the transfer of manufacturing of Devices and Combination Products from the Global Device Development (GDD) Group in R&D to commercial manufacturing sites as per the GDD design control process in compliance with ISO 13485 and 21 CFR 820. · ...

The Global Logistics Coordinator & SAP Administrator (part time, 6 months fixed term) role will impact: · Every day, we rise to the challenge to make a difference and here's how the · role will make an impact:Works as single point of contact for all internal customers on issue re ...

We are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. · The Manufacturing Operator role will make an impact by ope ...

We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. We empower people worldwide to live healthier at every stage of life. · Life cycle management and regulatory filing maintenance activities; · Preparation, review a ...

We do so via: Access Providing high quality trusted medicines regardless of geography or circumstance; Leadership Advancing sustainable operations and innovative solutions to improve patient health; and Partnership Leveraging our collective expertise to connect people to products ...

We are looking for a Manufacturing Operator to join our team at Viatris in Damastown. As a Manufacturing Operator , you will be responsible for safely carrying out production duties as directed in the assigned packaging area. · ...

Job summary · The Role & What You Will Be DoingConduct routine chromatographic (HPLC and GC, but primarily HPLC) and wet chemistry testing of raw materials, in process, finished product and stability samples in strict compliance with GLP & cGMP procedures. · ...

We are seeking a Head of Global Regulatory CMC Sciences to join our team at Viatris. · ...

We develop device technologies to enable drug-delivery for respiratory, biologic, biosimilar and injectable products. We operate from 4 sites: Dublin, Ireland,, Cambridge & Sandwich, UK and Southpointe,, Pittsburgh,, USA. · Provision of technical expertise to support the developm ...

We are seeking a Regulatory Affairs Manager to ensure global regulatory compliance and develop regulatory strategies. · The role involves ensuring alignment with external requirements and internal quality procedures, · demonstrating regulatory expertise, · collaboration, · and sh ...

We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. · ...

As part of our Allergy/Cardiovascular portfolio team, we are seeking an experienced Director to lead our regulatory strategy. This role will involve providing critical guidance on submissions to regulatory agencies. · Key Responsibilities: · Develop and implement effective regula ...

The Global Transportation Specialist role will make an impact by being the main point of contact for our Freight Bill & Audit Platform and working closely with Freight Bill and Audit provider to ensure Invoices are processed in timely manner. · Main point of contact for our Freig ...

The Quality Control (QC) Analyst III will be primarily responsible for the advanced chromatographic and wet chemistry analysis of raw materials, · in-process, finished product and stability product samples and completing the relevant GMP documentation.About this role: · Conduct r ...