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Product Development Engineer
Eingestellt von Experis AG
Gesuchte Skills: Engineering, Engineer, Design
Projektbeschreibung
PRODUCT DEVELOPMENT ENGINEER - ZUCHWIL - 100%
Experis is the global leader in professional resourcing and project-based workforce solutions. Our suite of services range from interim and permanent recruitment to managed services and consulting, enabling businesses to achieve their goals. We accelerate organisational growth by attracting, assessing and placing specialised professional talent.
For our international client based in Zuchwil, Experis is currently looking for a Product Development Engineer for a contracting position until the end of 2018.
General information:
- Start date: 01.02.2018
- End date: 31.12.2018
- Work location: Zuchwil
- Workload: 100%
Tasks & Responsibilities:
- be responsible for technical engineering support of different initiatives driven by manufacturing (transfers, harmonization, process changes, etc.).
- update registration relevant documentation of the Design History File to meet current standards and requirements (eg risk management documents, functional & design requirements, verification &validation activities).
- technically lead optimizations and design changes and ensure proper communication and timing with manufacturing and shared services.
- collaborate with the technical engineering office, write test methods and setups, complete testing requirements and write verification & validation reports.
Information exchange and collaboration between internal, local, external and foreign partners is essential. Close cooperation with internal departments, domestic and international authorities as well as the conscientious preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL).
You bring for this role the following qualifications:
- team player with strong initiative
- higher degree in engineering and would preferably have some practical experience in a regulated industry.
- self-motivated and take responsibility in your projects.
- creative problem-solver with excellent communication skills and strong leadership ability.
- you have a keen interest in the interrelations between medicine and technology and a strong desire to work in a global company
- ability to communicate in both spoken and written English & German is required.
Interested in this opportunity? Kindly send us your CV today through the link in the advert. However should you have any questions please contact Stéphanie Vogt.
Experis is the global leader in professional resourcing and project-based workforce solutions. Our suite of services range from interim and permanent recruitment to managed services and consulting, enabling businesses to achieve their goals. We accelerate organisational growth by attracting, assessing and placing specialised professional talent.
For our international client based in Zuchwil, Experis is currently looking for a Product Development Engineer for a contracting position until the end of 2018.
General information:
- Start date: 01.02.2018
- End date: 31.12.2018
- Work location: Zuchwil
- Workload: 100%
Tasks & Responsibilities:
- be responsible for technical engineering support of different initiatives driven by manufacturing (transfers, harmonization, process changes, etc.).
- update registration relevant documentation of the Design History File to meet current standards and requirements (eg risk management documents, functional & design requirements, verification &validation activities).
- technically lead optimizations and design changes and ensure proper communication and timing with manufacturing and shared services.
- collaborate with the technical engineering office, write test methods and setups, complete testing requirements and write verification & validation reports.
Information exchange and collaboration between internal, local, external and foreign partners is essential. Close cooperation with internal departments, domestic and international authorities as well as the conscientious preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL).
You bring for this role the following qualifications:
- team player with strong initiative
- higher degree in engineering and would preferably have some practical experience in a regulated industry.
- self-motivated and take responsibility in your projects.
- creative problem-solver with excellent communication skills and strong leadership ability.
- you have a keen interest in the interrelations between medicine and technology and a strong desire to work in a global company
- ability to communicate in both spoken and written English & German is required.
Interested in this opportunity? Kindly send us your CV today through the link in the advert. However should you have any questions please contact Stéphanie Vogt.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik