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Auditor
Eingestellt von Experis AG
Gesuchte Skills: Engineering, Client
Projektbeschreibung
AUDITOR - NEAR SOLOTHURN - 100%
Experis is the global leader in professional resourcing and project-based workforce solutions. Our suite of services range from interim and permanent recruitment to managed services and consulting, enabling businesses to achieve their goals. We accelerate organisational growth by attracting, assessing and placing specialised professional talent.
For our international client based near Solothurn, Experis is currently looking for an Auditor for a contracting position of, at least, 6 months.
TasksISO EN 13485:2016; MDD; other applicable regulations
- Writing of internal and reports and creation of relevant documentation
- Follow up of internal and external audit observation to assure appropriate and timely implementation of Corrective Actions
- Provide Regulatory Compliance support in all areas of Quality System Elements
- Documentation review in Quality System relevant areas
You bring for this role the following qualifications:
- Previous experience in a similar position in auditing in the medtech or pharma
- A qualification as an auditor within the medtech is highly appreciated and as well the training in the new ISO 13485:2016
- Fluent English
- Strong tracking, coordination and project planning skills
- Master and/or Bachelor Degree in Mathematics, Engineering, Computer Science or Chemistry ...
Interested in this opportunity? Kindly send us your CV today through the link in the advert. However should you have any questions please contact Stéphanie Vogt.
Experis is the global leader in professional resourcing and project-based workforce solutions. Our suite of services range from interim and permanent recruitment to managed services and consulting, enabling businesses to achieve their goals. We accelerate organisational growth by attracting, assessing and placing specialised professional talent.
For our international client based near Solothurn, Experis is currently looking for an Auditor for a contracting position of, at least, 6 months.
TasksISO EN 13485:2016; MDD; other applicable regulations
- Writing of internal and reports and creation of relevant documentation
- Follow up of internal and external audit observation to assure appropriate and timely implementation of Corrective Actions
- Provide Regulatory Compliance support in all areas of Quality System Elements
- Documentation review in Quality System relevant areas
You bring for this role the following qualifications:
- Previous experience in a similar position in auditing in the medtech or pharma
- A qualification as an auditor within the medtech is highly appreciated and as well the training in the new ISO 13485:2016
- Fluent English
- Strong tracking, coordination and project planning skills
- Master and/or Bachelor Degree in Mathematics, Engineering, Computer Science or Chemistry ...
Interested in this opportunity? Kindly send us your CV today through the link in the advert. However should you have any questions please contact Stéphanie Vogt.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik