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Validation Engineer (Medical Device Sector)
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Engineer, Engineering, Consultant
Projektbeschreibung
Role: Quality Engineer, Validation Consultant
Place of work: Oberdorf, Baselland
Project start date: 23.01.2017
Project end date: 31.12.2017
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.
Place of work: Oberdorf, Baselland
Project start date: 23.01.2017
Project end date: 31.12.2017
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.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Organisation/Management