Validation Engineer (Medical Device Sector)

Vertragsart:
Vor Ort
Start:
keine Angabe
Dauer:
keine Angabe
Von:
Harvey Nash IT Recruitment Switzerland
Ort:
Nidwalden
Eingestellt:
06.01.2017
Land:
flag_no Schweiz
Projekt-ID:
1264272

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Role: Quality Engineer, Validation Consultant

Place of work: Oberdorf, Baselland

Project start date:

Project end date:

Workload/weekly working hours: 100%/40 hours

Validation Engineer to provide support for Functional Test Method Validation activities associated with Mechanical and Materials Test Methods.

Primary Tasks and Responsibilities:

. Serves as technical expert for the Validation process and responsibilities to ensure compliance
. Writes, reviews and approves Validation Plans, Summary Reports and other documentation associated with validations
. Ensures that all validation activities are carried out and reported in a timely manner.
. Facilitates, encourages and coordinate continuous improvement with respect to validation activities.
. Execute Mechanical Testing projects

Requirements:

. High understanding of GMP, Compliance, and Validation Practices. Experience with Mechanical Testing is desirable
. Qualification in an appropriate discipline (eg Engineering or Life Science with additional technical qualification) with a broad technical/educational skills base

Non-Technical Profile Requirements:

. Must be able to lead and give direction to Validation Projects.
. Minimum of 2 years working in a regulated environment, a minimum 1 of which has been spent carrying out validation activities.
. English and German spoken and written.