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Human Factors Engineer Intern

MEDA Pharma GmbH & Co. KG
Pay: Competitive
Internship Type:
Length of Scheme: Unknown
Deadline date: Unknown
Location: Cambridge Cambridge United Kingdom
Category: Internship
Available from: Immediately
Finishes on: Ongoing Position
Type of work: Full Time, Indoor , Daytime Work
Job reference: E03932754
Engineering 2021-05-17 2021-06-23

Job Description

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 Device Development organisation is focused on the design, development and commercialisation of a diverse portfolio of device technology solutions to enable delivery for our large and growing generic and branded products around the globe. We develop device technologies to enable drug-delivery for respiratory, biologic, biosimilar and injectable products, and work across Viatris to support innovative technology solutions to provide healthcare solutions for our patients. We operate from 4 sites: Dublin, Ireland, Cambridge & Sandwich, UK and Southpointe, Pittsburgh, USA. Every member of our team is dedicated to creating better health for a better world, one person at a time. Every day, we rise to the challenge to make a difference and here’s how the Human Factors Engineer Internship role will make an impact: Key responsibilities for this role include: Support a number of usability engineering programs; maintaining a current view of how FDA Quality Systems-Design Control requirements, IEC 62366, AAMI/ANSI HE75 are integrated in the process for developing high-quality combination products. Support User Interface design including Instructions for Use and Packaging. Support User Research into combination device users, intended use, user needs and use issues encountered with similar devices. Support the development of human factors usability evaluations from study design, sample preparation, use error root cause analysis, report reviews to results analysis. Input qualitative and quantitative user data into Viatris’s Risk Management program. Investigate and assess current databases to track and monitor marketed device combination product complaints on a range of global products. The minimum qualifications for this role are: Currently enrolled or a recent graduate at a Human Factors, Design or Engineering degree program, or a related field of study at an accredited college or university. In depth knowledge of how Human Factors Engineering plays a key role in medical device development and integration into device design control. Proficient in Microsoft Office, specifically Excel, Word and Powerpoint. Familiar with Adobe Illustrator, InDesign and Photoshop. The ability to produce quality output within tight deadlines. Effective presentation skills, both written and verbal. Strong analytical skills, able to digest complicated data, perform analysis and produce clear findings. Comfortable working independently with minimal supervision. Proficiency in speaking, comprehending, reading and writing English is required. 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.

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