1997

Technical Operation Engineer (m/w)

Für wen suchen wir

Unser Kunde ist ein internationales Unternehmen der Pharma- und Logistikbranche.

Ort

65451 Kelsterbach

Frei ab

sofort

Vertragsart

befristet

Beschäftigungsart

Vollzeit

Option auf Übernahme

vorhanden

Arbeitszeiten

  • Vollzeit (40 Stunden/Woche)
  • Arbeitszeiten: Mo-Fr
  • Beginn: ab sofort

Vergütung

nach Absprache - Branchenüblich 

Der Job

  • Generation and review of validation documents (URS, DQ, IQ, OQ, PQ).
  • Train Depot Operations before validation activities to ensure Marken, global and technical standards.
  • Train Depot Operations on corrective and preventative actions to ensure improvements.
  • Facilitate and perform Risk Assessments as required
  • Training of team members
  • Verification processes of the Depot operations
  • Oversight and follow up of the annual maintenance schedule  and arrangements of the equipment maintenances with the maintenance providers
  • Performing investigations regarding area non-conformances and implementation of appropriate actions to prevent recurrence
  • Participation on the improvement processes for the Depot operations, SOPs and all related to the execution of activities in the depot.
  • Implementation of area KPIs and continuous improvement initiatives
  • Take over responsibilities in creating and writing of SOP´s Training material
  • Ensure performance maintenance and back up for Central Monitoring system
  • Ensure the compliance with the requirements of GMPs
  • Support client audits and regulation audits
  • Take over Depot Operation task as Reception, Processing of returns, Preparation of Returns
  • Prepare Processing of stock control including periodic cycle counts
  • Support on the follow up of the annual maintenance schedule  and arrangements  of the equipment maintenances with the maintenance providers
  • Participation on the improvement processes for the Depot operations, SOPs and all related to the execution of activities in the depot.
  • Implementation of area KPIs and continuous improvement initiatives

Das bringen Sie mit

  • Bachelor degree level in the careers of: Logistics, Pharmacy, Life Science, Engineering
  • A minimum of 2-3 years of experience in a clinical trials supplies environment including validation and process improvements
  • Proficiency in Microsoft Office applications (in particular Excel)
  • Knowledge of validation and Qualification processesl
  • Good command of English
  • Strong team, and individual management skills
  • Good knowledge of GxP requirements

Kontaktinformationen

Herr Sascha Wittig
Office Events P & B GmbH
Freseniusstraße 29
65193 Wiesbaden

Bewerbungsinformationen

Sie verfügen über die oben genannten Kenntnisse und möchten diesen Aufgabenbereich mit Engagement, Spaß und Teamgeist übernehmen?

Dann warten Sie nicht länger. Das Office Events Team freut sich über Ihre Bewerbung.

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