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Senior QA Associate
This vacancy has now expired. Please see similar roles below...
A leading biopharmaceutical company is seeking a Senior QA Associate to join their team in Breda, Netherland.
Job Role:
- Act as the first point of contact in case of production queries (quality related) during packaging and labeling operations.
- Work together with production and maintenance team to resolve the quality related problems.
- Review and approve class I Non Conformances
- Review and approve batch record exception reports
- Coach production and maintenance staff to improve on quality and to limit number of errors
- Perform finished product checks during (commercial) production runs
- Complete batch release preparation prior to Qualified person disposition.
Education, Skills and Experience:
- EU Pharmacist degree (or equivalent) is required (e.g. BIG registered)
- Preferably 0.5 year of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations.
- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.
- Manufacturing and/or Quality analytical processes and operations.
- Fluent in English language. Systems
- TrackWise (NC/CAPA)
- MS Office (Word, Excel) Werum PAS-X (electronic batch Records)
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Caleb Mensah on +44 203 854 1080 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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