Intern - Device Development Assurance

Posted on June 26, 2023 by InternPlug

  • Other
  • 1 Vacancy

Job Description

1484 McDermott Laboratories Limited At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

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.
About Your Skills & Experience For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:
  • 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.
At Viatris, 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. You may just be the right candidate for this or other roles. Diversity & Inclusion at Viatris At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at Viatris Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Viatris is an Equal Opportunity Employer.

Advertised until:
July 26, 2023

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