Support new product regarding design control related activities for the development of medical device / combination products and support process development activities within the line function as part of the Novartis Global Device Development & Commercialization organization
Lead creation of development documentation strategy for the project including the list of required documents in order to comply with the applicable regulations
Subject matter expert responsible for independently supporting projects utilizing Design Control expertise
Ownership of the commercial design history file to ensure documents are maintained through the life cycle of the product
The position offers opportunities to work in multidisciplinary teams, across projects, where specific contribution within the development and life cycle management process is a key element for success
Education : University degree (Bachelor’s degree or higher) in Mechanical Engineering, Biotechnology, Biomedical Engineering, Medical Technology or similar
Languages : English fluent / German beneficial
Experience : Minimum 3 years of experience in pharmaceutical or medical device industry in the development, submission and commercialization of medical or drug delivery devices as a quality engineer or development engineer;
vast experience in writing / reviewing design control documents and compilation of design history files
Contact : Alexandra Paul, Recruiter
We offer a market-competitive base salary in line with your qualification, experience and individual competencies. Additionally, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning & development options and worldwide career opportunities within the Novartis group.
The base pay is composed of a market oriented excess payment and the respective amount according to the Austrian collective agreement (at least € 48,718.
04 per year on a full time basis).