Beschreibung
Für unseren Kunden in Süddeutschland suchen wir Unterstützung im Bereich Deviation & Capa Management.Start: ASAP
Umfang: Vollzeit
Laufzeit: bis Ende des Jahres
Job requirements:
- Job-focus is on management of deviations and CAPA (corrective and preventive actions) management as well as complaints to ensure the timely evaluation of deviations and complaints and that the resulting actions are reasonably set and provided
- Conduction of training with regard to compliance to regulations and handling of deviations (for example certifications as investigators) and complaints according to company regulation
- Project lead and support of other departments on GMP-compliance related issues at manufacturing and analytical processes. Contributes pharmaceutical expertise in area of responsibility
- Create and review GMP relevant documents in own area of responsibility (e.g. SOPs, procedures, reports, records, third party work)
- Provide support to internal policies (GOPs, Manual) and global compliance initiatives.
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