Intern - Device Development Assurance
Posted on June 26, 2023 by InternPlug
- Dublin, Ireland
- No Salary information.
- Full Time
Viatris empowers people worldwide to live healthier at every stage of life.
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 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 world. The Role & What You Will Be Doing Support the general maintenance and improvement of the Global Device Development Quality Management System, with particular focus on execution of activities to enhance the usability of the existing GDD Document Management System and the further development of the Combination / Medical Devices products List. Every day, we rise to the challenge to make a difference and here’s how the Intern - Device Development Assurance role will make an impact:
- Support the general maintenance and improvement of the Global Device Development Quality Management System.
- Supporting the ongoing continuous improvement of Document Control processes / procedures in accordance with department and company goals.
- Supporting the implementation of upgrades to the GDD Document management system.
- Supporting third party inspections / audits.
- Project: Executing project to link SOPs and Forms in Documentum to enhance available search and SOP update functionality in Documentum to enhance the user experience and create additional efficiency in the SOP / Form / Work Instruction Update process.
- Project: Executing project to create and update existing MyUni Curricula to create efficiency in assignment of read and understand training to new starters in GDD and enhance the induction training experience for new starters.
- Project: Supporting the development & enhancement of the Combination Products / Medical Devices List to take account of new and emerging regulatory reporting requirements.
- Project: Supporting the development of a process to acquire and assess proposed updates and updates to relevant standards / regulations / guidance documents and pharmacopeia monographs and ensure these are transmitted internally in GDD and ultimately reflected in the relevant GDD SOPs / Wis / Forms and documents.
- Have Completed, or presently undertaking, a 3rd-Level course of study in the area of engineering / life sciences / quality assurance / regulatory science
- Strong problem solving and analytical skills.
- A team player willing to support any other organisational needs/activities outside primary expertise to continuously develop the business.
- Previous placement / experience in a Quality Management System driven organization.
- Experience with Document and Record control practices, Data Integrity and Good.
- Documentation practices.
- Previous experience with Enterprise software packages such as Documentum, MyUniversity and TrackWise™.
- Individuals with a keen interest in medical device / combination product development and / or Quality Assurance or Regulatory principals very desirable.
Advertised until:
July 26, 2023
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