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Product Quality Engineer
Eingestellt von ITech Consult
Gesuchte Skills: Engineer, Support
Projektbeschreibung
PRODUCT QUALITY ENGINEER
About us:
ITech Consult AG is a certified ISO 9001/2008 Swiss company with offices also located in Germany, Great Britain and Ireland. ITech Consult is specialised in delivering ICT 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.
REFERENCE NO: 916967NC
ROLE: Product Quality Engineer
DOMAIN: Pharma
LOCATION: Luzern und region, Switzerland
JOB TYPE: Contract.
WORKLOAD: 100%
START DATE: ASAP
DURATION: 31/12/2018
JOB DESCRIPTION:
Summary:
Looking for someone who is responsible for editing and technical review of deviations, as well as technical release of the assigned products. Assistance in troubleshooting the allocated analysis system in the case of complex error messages.
RESPONSIBILITIES:
- Ensuring and checking the product quality during system development and the subsequent production of the system.
- Responsible for the evaluation and analysis of quality data (eg right first time, error messages) as well as the relevant meetings in the product management team.
- Create, update, and drop default documents, statements and reports, training, and technical support of staff in the laboratory and share.
- Identification and presentation of measures for improvement and implementation in consultation with the product team.
- Coordination of the tasks in the equipment management process and support of the authorities.
REQUIRED SKILLS:
- Minimum 3 years of experience working with Pharma or Diagnostics or Molecular Biology labs.
- Experience in a regulated GxP environment ideally of medical technology (ISO 13458, GMP, FDA 21 CFR 820) in deviation management.
- You appreciate independent and responsible work in a versatile product and project environment.
- Have an acute sense for quality and a structured and scientific approach is natural for you.
- Technical flair and understanding in dealing with the products (analysers), text systems and test software.
NICE TO HAVE:
- Understanding of Complex Hardware and Software Architectures are advantageous.
- SAP Knowledge is an advantage.
EDUCATION: Bachelor or Master Degree in Science or Technical field.
LANGUAGES: Fluent in German and English language.
SHOULD YOU FIND YOURSELF SUITABLE FOR THIS POSITION THEN SEND YOUR COMPLETE DOSSIER USING THIS LINK IN THE ADVERT.
CALL US AND DISCOVER THE QUALITY OF OUR SERVICES FOR YOURSELF. WE ARE MORE THAN HAPPY TO MEET WITH YOU FOR AN INDIVIDUAL CONSULTATION. DO NOT HESITATE TO CONTACT US FOR FURTHER ENQUIRES.
OUR PAY ROLLING IS REFERRED BY 98% OF OUR FREELANCERS AS THE BEST PAY ROLLING SYSTEM IN SWITZERLAND. DO YOU REQUIRE MORE INFORMATION? FEEL FREE TO CONTACT US.
About us:
ITech Consult AG is a certified ISO 9001/2008 Swiss company with offices also located in Germany, Great Britain and Ireland. ITech Consult is specialised in delivering ICT 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.
REFERENCE NO: 916967NC
ROLE: Product Quality Engineer
DOMAIN: Pharma
LOCATION: Luzern und region, Switzerland
JOB TYPE: Contract.
WORKLOAD: 100%
START DATE: ASAP
DURATION: 31/12/2018
JOB DESCRIPTION:
Summary:
Looking for someone who is responsible for editing and technical review of deviations, as well as technical release of the assigned products. Assistance in troubleshooting the allocated analysis system in the case of complex error messages.
RESPONSIBILITIES:
- Ensuring and checking the product quality during system development and the subsequent production of the system.
- Responsible for the evaluation and analysis of quality data (eg right first time, error messages) as well as the relevant meetings in the product management team.
- Create, update, and drop default documents, statements and reports, training, and technical support of staff in the laboratory and share.
- Identification and presentation of measures for improvement and implementation in consultation with the product team.
- Coordination of the tasks in the equipment management process and support of the authorities.
REQUIRED SKILLS:
- Minimum 3 years of experience working with Pharma or Diagnostics or Molecular Biology labs.
- Experience in a regulated GxP environment ideally of medical technology (ISO 13458, GMP, FDA 21 CFR 820) in deviation management.
- You appreciate independent and responsible work in a versatile product and project environment.
- Have an acute sense for quality and a structured and scientific approach is natural for you.
- Technical flair and understanding in dealing with the products (analysers), text systems and test software.
NICE TO HAVE:
- Understanding of Complex Hardware and Software Architectures are advantageous.
- SAP Knowledge is an advantage.
EDUCATION: Bachelor or Master Degree in Science or Technical field.
LANGUAGES: Fluent in German and English language.
SHOULD YOU FIND YOURSELF SUITABLE FOR THIS POSITION THEN SEND YOUR COMPLETE DOSSIER USING THIS LINK IN THE ADVERT.
CALL US AND DISCOVER THE QUALITY OF OUR SERVICES FOR YOURSELF. WE ARE MORE THAN HAPPY TO MEET WITH YOU FOR AN INDIVIDUAL CONSULTATION. DO NOT HESITATE TO CONTACT US FOR FURTHER ENQUIRES.
OUR PAY ROLLING IS REFERRED BY 98% OF OUR FREELANCERS AS THE BEST PAY ROLLING SYSTEM IN SWITZERLAND. DO YOU REQUIRE MORE INFORMATION? FEEL FREE TO CONTACT US.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges