Hays – Working for your tomorrow | Germany | Mannheim | Full time | Published since: 06.03.2025 on stepstone.de
Spezialist Batch Record Review (m/w/d)
With over 15 years of experience in the classic pharmaceutical industry, biotechnology, chemistry and medical technology, we know the key contact persons who write out demanding tasks with potential. The high demand for personnel opens up exciting opportunities for dedicated professionals and managers to develop professionally and work on their own careers. As a specialized staff consultancy with an international network, we offer you decisive advantages - and this is completely free of charge for you. Register and benefit from interesting and matching positions and projects. JOBV1_EN
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With over 15 years of experience in the classic pharmaceutical industry, biotechnology, chemistry and medical technology, we know the key contact persons who write out demanding tasks with potential. The high demand for personnel opens up exciting opportunities for dedicated professionals and managers to develop professionally and work on their own careers. As a specialized staff consultancy with an international network, we offer you decisive advantages - and this is completely free of charge for you. Register and benefit from interesting and matching positions and projects.
Operational transparency of batch papers Control of the filled HABs (also rebookings) on GMP-compliant documentation including tracking of timely correction by the responsible companies Strict compliance with OLT (Order Lead Time) including tracking and requesting the required HAB accompanying documents such as IPC sheets, audit trails, trending and EMT reports Participation in the processing of measures from GMP requirements (e.g. search for deviation etc.) Support for GMP audits e.g. by participation in the War-Room Support for actions on inspections or QRBs/DRs (e.g. HAB searches in the archive) Revision and creation of documentation-relevant SOPs in consultation with the supervisor Implementation of training on documentation-relevant SOPs or HEA changes in agreement with the supervisor and the operation
Successfully completed training as a pharmacist (m/w/d) or comparable training Professional experience in the pharmaceutical environment, especially in Parenteralia Production Very good knowledge of GMP regulations and GMP-compliant documentation as well as hygiene knowledge in the pharmaceutical field Very high level of quality awareness Funded IT system knowledge (MES, SAP, Excel, Word) Good communication and team skills, organizational skills, sense of responsibility and process knowledge Clear written and oral expression in German as well as good oral and written English skills
Working in an international company 30 days off JOBV1_EN
Company location
Location
| Hays – Working for your tomorrow | |
| Mannheim | ||
| Germany |
The text of this ad was translated from German into English using an automatic translation system and may contain semantic and lexical errors. Therefore, it should be used for introductory purposes only. For more detailed information, see the original text of the ad at the link below.
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