Beschrijving vacature

NNE PHARMAPLAN A/S

Gentofte, 1 stilling

If you have been working within medical device design for some years now, and you would like to broaden you competencies and take on more responsibility – here is your opportunity.



Your job



NNE Pharmaplan has established a Global Drug Delivery/Medical Device competence centre, working from Copenhagen with clients in Denmark, Central Europe, and the United States. We have been developing patient-centric medical device solution for several decades and have expanded our business globally over the last three years.



We see a huge demand for our expertise and are looking for medical device engineers with the potential of becoming one of our Senior Technology Partners in a few years.



We are looking for candidates that have been involved in the early development stages and who also have the very important expertise of detailed design work; bringing a user-friendly device to the manufacturing stage. Essentially, we are looking for candidates who can close the loop between concepts and real-life manufacturing realities. The job requires the ability to bridge the theoretical and practical experience in the process of designing a device that improves the quality of life for patients and improves the daily operation for trained nurses, doctors, etc.



You will be part of a team of internationally acknowledged medical device engineers and consultants who are involved in defining the international standards of the future and are key note speakers at international conferences and events. They will be your mentors and support you in taking the next step in your career.



Your Qualifications



You have a Bachelor’s Degree in Engineering or Science and an advanced degree is a plus. Furthermore, you typically have 4+ years of experience within the field of medical devices/drug delivery.



We are looking for candidates who are flexible with regards to travel and willing to go the extra mile to find the right solution



General characteristics:

•Fluency in English, other languages a plus

•Proficiency in FDA (21 CFR part 820) and EU (ISO 13485, ISO 14971) regulations

•History of ensuring GMP compliance including: input requirement development, maintenance and review, Formative and Summative studies, clinical validation, traceability matrix from design input through V&V testing, SOPs, manufacturability, and CAPA processes

•Concept and prototype development skills

•Pharmaceutical and Biotech drug delivery experience is a plus, e.g., needle, dual chamber, and injector development

•CAD modelling; SolidWorks and or Creo



Contact



For further information, please contact Carsten Bech Vice President for Drug Delivery, +45 30751818 or Stephen Fournier, Senior Technology Partner, +45 30754947.



Application



Please submit your application online via http://www.nnepharmaplan.com

Functiebeschrijving
Sector:
Human health and social work activities
Beroepsveld:
Engineering professionals (excluding electrotechnology)
Work experience:
Work experience is not required
Salaris van/tot:
Not provided
Date of expiry: