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Projektbeschreibung
QA Executive for leading Pharmacutical & Medical Device company in the North West
An exciting new opportunity has become available for an enthusiastic QA Executive with technical writing expereince for a leading Medical Device company. Candidates will be expected to be organised with a keen attention to detail.
QA Executives responsibilities will be;
File generation during the design and transfer to manufacturing processes
* Production of procedures and technical reports as part of the development cycle of new products
* Investigations and investigation report
* Technical writing to ensure timely delivery of design verification protocols, validation protocols, test summary reports and technical file generation.
* Document Control and Change Management
Technical Authors main requirements will be;
* Technical understanding of product development lifecycles
* Candidate must possess excellent written and oral communication skills
* Scientific or technical knowledge,
* Medical Device experience
* ISO 13485 and Medical Device Quality System regulations
I am very interested in discussing your future availability to contract work and talking through latest CV. Rest assured, discretion shall be applied at all times. Call on +44 (0)207 7758 7322 or email me at find out more about Real Staffing please visit www.realstaffing.com
An exciting new opportunity has become available for an enthusiastic QA Executive with technical writing expereince for a leading Medical Device company. Candidates will be expected to be organised with a keen attention to detail.
QA Executives responsibilities will be;
File generation during the design and transfer to manufacturing processes
* Production of procedures and technical reports as part of the development cycle of new products
* Investigations and investigation report
* Technical writing to ensure timely delivery of design verification protocols, validation protocols, test summary reports and technical file generation.
* Document Control and Change Management
Technical Authors main requirements will be;
* Technical understanding of product development lifecycles
* Candidate must possess excellent written and oral communication skills
* Scientific or technical knowledge,
* Medical Device experience
* ISO 13485 and Medical Device Quality System regulations
I am very interested in discussing your future availability to contract work and talking through latest CV. Rest assured, discretion shall be applied at all times. Call on +44 (0)207 7758 7322 or email me at find out more about Real Staffing please visit www.realstaffing.com
Projektdetails
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Einsatzort:
North West England, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Medien/Design