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Quality Assurance Officer
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Client
Projektbeschreibung
To perform site wide self-inspections as lead auditor and promote continuous improvement across all disciplines.
Ensure compliance to GMP, GCP and GLP throughout the company.
In conjunction with Operations, critically assess deviations and customer complaints to ensure closure in a timely manner.
To assist with client inspections.
To perform batch documentation review of the critical process parameters of manufacturing, packaging and distribution operations to ensure compliance with written specifications, SOP's GMP and GDP.
To provide KPI's for batch review and manage priorities/workload to ensure that batches are received and released in a timely manner to meet customer expectation.
Be fully competent to train others in batch documentation review of critical process parameters of the Manufacturing, Clinical and Packaging batches.
To ensure that following QA review that the batch is suitable for progression to the QP.
Deliver GMP training to site.
Respond to client requests and batch comments in a timely manner and measure/act on these metrics.
Qualifications/Experience:
The job holder will have significant (ideally more than 10 years) experience in the pharmaceutical industry, with a diverse knowledge of various dosage forms manufacturing and experience of meeting client deadlines.
Excellent written and verbal communication skills are essential. The job holder will need to communicate with personnel outside of the Quality group, with external clients, in order to ensure timely completion of business demands and customer service.
To find out more about Real Staffing please visit www.realstaffing.com
Projektdetails
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Einsatzort:
South Wales, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung