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Quality Engineers, Validation Consultant
Eingestellt von Experis AG
Gesuchte Skills: Consultant, Engineer
Projektbeschreibung
QUALITY ENGINEERS, VALIDATION CONSULTANT
New aspiration? New work environment? New horizon? New Job?
Why don't you look at what Experis can offer you?!
One of the biggest Medical Devices Company based in Oberdorf is looking for a QUALITY ENGINEER/VALIDATION CONSULTANT for a contracting role starting in the mid of January until the end of THE YEAR.
In overall, you as a QUALITY ENGINEER/VALIDATION CONSULTANT will be responsible for the validation process and responsibilities to ensure compliance. You will also write reviews and approve Validation Plans, Summary Reports and other documentation associated with validations. Furthermore, you will ensure that all validation activities are carried out and reported in a timely manner, facilitates, encourages and coordinate continuous improvement with respect to validation activities. Finaly, you will execute mechanical testing projects.
THIS ROLE REQUIRES:
- High understanding of GMP, COMPLIANCE, AND VALIDATION PRACTICES
- Good experience with Mechanical Testing
- QUALIFICATION EXPERIENCE
- Experienced in validation projects.
- Minimum 2+ YEARS' experience in a REGULATED ENVIRONMENT
- Medical devices experiences is a plus
- FLUENT ENGLISH AND GERMAN
Are you a QUALITY ENGINEER/VALIDATION CONSULTANT with excellent ANALYTICAL SKILLS, looking for a challenging position in a dynamic and well known company then we looks forward to receiving your application!
Further information on the role? Call Julie Mackerer.
New aspiration? New work environment? New horizon? New Job?
Why don't you look at what Experis can offer you?!
One of the biggest Medical Devices Company based in Oberdorf is looking for a QUALITY ENGINEER/VALIDATION CONSULTANT for a contracting role starting in the mid of January until the end of THE YEAR.
In overall, you as a QUALITY ENGINEER/VALIDATION CONSULTANT will be responsible for the validation process and responsibilities to ensure compliance. You will also write reviews and approve Validation Plans, Summary Reports and other documentation associated with validations. Furthermore, you will ensure that all validation activities are carried out and reported in a timely manner, facilitates, encourages and coordinate continuous improvement with respect to validation activities. Finaly, you will execute mechanical testing projects.
THIS ROLE REQUIRES:
- High understanding of GMP, COMPLIANCE, AND VALIDATION PRACTICES
- Good experience with Mechanical Testing
- QUALIFICATION EXPERIENCE
- Experienced in validation projects.
- Minimum 2+ YEARS' experience in a REGULATED ENVIRONMENT
- Medical devices experiences is a plus
- FLUENT ENGLISH AND GERMAN
Are you a QUALITY ENGINEER/VALIDATION CONSULTANT with excellent ANALYTICAL SKILLS, looking for a challenging position in a dynamic and well known company then we looks forward to receiving your application!
Further information on the role? Call Julie Mackerer.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Organisation/Management