Requirement Engineer - IVD/Diagnostics/CPRE/IREB/CCBA

Luzern  ‐ Vor Ort
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Beschreibung

Requirement Engineer: IVD/Diagnostics/CPRE/IREB/CCBA/IIBA/Medical Devices/English

Role Purpose: Our client is looking for a Required Engineer with a background in IVD development.

Job Responsibilties & Requirements:

- Should have at least 5 years of experience working as a Requirements Engineer in Diagnostics Environment.
- Should have at least 5 years of experience handling the multiple projects on the whole development process.
- Good experience working in regulated environment and functions and dependencies in IVD development.
- Responsible for elicitation of customer and internal stakeholder requirements.
- Responsible to cooperate with usability engineering in process analysis.
- Leadership to drive cross functional team alignment and support of team decisions in engineering process.
- Responsible to transfer of product requirements into technical and software requirements in cooperation with receiving department (instrument, reagent, software development)
- Documentation and change management of requirements
- Contribution to assessment of changes and its impact on technical and software requirements
- Responsible to support of product risk assessment.

IT Skills:

- Good experience in application management tools (ideally HP ALM), tools for analysis, interpretation of data and visualization (like MS access, visio, office)
- Strong analytical thinking, ability to see the big picture as well as the details (ia separation of requirements, breakdown structures)
- Should have good experience in moderating peers and stakeholders.

Education:

- Bachelor/Master (BSc/MSc) in Engineering, Biotechnology or equivalent.
- Knowledge of engineering approaches and tools (Application Lifecycle Management Tools).
- Certification in CPRE/IREB and/or CCBA/IIBA (foundation level/capability level).

Languages:

- Fluent in English (Writtern & Oral).
- Fluent in German

Reference No .: 917568NC

Role: Requirement Engineer: IVD/Diagnostics/CPRE/IREB/CCBA/IIBA/Medical Devices/English

Domain:
Pharma

Location:
Lucerne and region, Switzerland

Workload:
100%

Start Date:


Duration: Till

Should you find yourself suitable for this position then please send us your complete CV using the link in this advert.

If the position is not a perfect match and you wish to receive other opportunities directly,you can send us your CV anyway via this advert or to jobs[at]itcag[dot]com.

About us:

ITech Consult is a certified ISO 9001:2008 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.

Start
ab sofort
Dauer
Till 31.12.2018
Von
ITech Consult
Eingestellt
12.07.2018
Projekt-ID:
1596993
Vertragsart
Freiberuflich
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