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Quality Assurance Manager
Eingestellt von ITech Consult
Gesuchte Skills: Support, Sap
Projektbeschreibung
Quality Assurance Manager
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.: 916461NC
ROLE: Quality Assurance Manager
INDUSTRY: Pharma
LOCATION: Luzern und Region; Switzerland
WORKLOAD: 100%
START DATE: ASAP
DURATION: Till 31.12.2017
JOB DESCRIPTION:
SUMMARY:
Assure that qualification, validation, equipment management activities as well as CSV Activities within the area of responsibility of the department are completed in time and documented in a traceable manner. Assure that corrective and preventive action as well as effectiveness checks within the area of responsibility (eg SCAR cases) of the department are completed in time and documented in a traceable manner.
Job Responsibilities:
-Support and consult the business partners of the department in the area of qualification, validation, equipment management as well as CSV activities as assigned.
-Assurance and continuous monitoring of cGMP compliance (eg FDA, IVDD, ISO) at RDI within the area of responsibility of the department.
-Support and performance of assigned, general and specific tasks within the area of responsibility of the department.
-Performance of trainings within the area of responsibility of the department.
Skills:
-At least 5 years of experience in area of medical devices and especially Supplier Quality and Qualification & Validation.
-Monitoring and Tracking of SCAR cases (Supplier Corrective Action Requests) according to daily business.
-Handling and/or review of Periodic Reviews (Qualification, Validation, CSV) according to daily business.
Nice to Have:
-SAP user ID
-Sharepoint
-MS Office
-Temporary support for SCARs and Q&V topics in Team Q&V and Supplier Quality
Education:
-Higher Education, such as Bachelor Degree in Computer Science or similar
-Qualification for Supplier Quality topics or similar
-Qualification for Qualification & Validation or similar
LANGUAGES: Excellent spoken and written German and English
Should you find yourself suitable for this position then send your complete dossier using this link in the advert.
Even if this position doesn't suit your profile we recommend that you send us your CV and share with us what you are exactly looking for.
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.: 916461NC
ROLE: Quality Assurance Manager
INDUSTRY: Pharma
LOCATION: Luzern und Region; Switzerland
WORKLOAD: 100%
START DATE: ASAP
DURATION: Till 31.12.2017
JOB DESCRIPTION:
SUMMARY:
Assure that qualification, validation, equipment management activities as well as CSV Activities within the area of responsibility of the department are completed in time and documented in a traceable manner. Assure that corrective and preventive action as well as effectiveness checks within the area of responsibility (eg SCAR cases) of the department are completed in time and documented in a traceable manner.
Job Responsibilities:
-Support and consult the business partners of the department in the area of qualification, validation, equipment management as well as CSV activities as assigned.
-Assurance and continuous monitoring of cGMP compliance (eg FDA, IVDD, ISO) at RDI within the area of responsibility of the department.
-Support and performance of assigned, general and specific tasks within the area of responsibility of the department.
-Performance of trainings within the area of responsibility of the department.
Skills:
-At least 5 years of experience in area of medical devices and especially Supplier Quality and Qualification & Validation.
-Monitoring and Tracking of SCAR cases (Supplier Corrective Action Requests) according to daily business.
-Handling and/or review of Periodic Reviews (Qualification, Validation, CSV) according to daily business.
Nice to Have:
-SAP user ID
-Sharepoint
-MS Office
-Temporary support for SCARs and Q&V topics in Team Q&V and Supplier Quality
Education:
-Higher Education, such as Bachelor Degree in Computer Science or similar
-Qualification for Supplier Quality topics or similar
-Qualification for Qualification & Validation or similar
LANGUAGES: Excellent spoken and written German and English
Should you find yourself suitable for this position then send your complete dossier using this link in the advert.
Even if this position doesn't suit your profile we recommend that you send us your CV and share with us what you are exactly looking for.
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:
SAP Entwicklung, Sonstiges