Pharma Operations Specialist: Non-Conformance & Quality Impact

Johnson & Johnson

Lavamünd

Vor Ort

EUR 74.000 - 95.000

Vollzeit

Vor 8 Tagen
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Zusammenfassung

Johnson & Johnson via Cilag AG seeks an Operations Specialist - Non-Conformances Coordinator at the Schaffhausen site to manage deviations, drive root-cause analysis, and implement CAPAs in close collaboration with QA and manufacturing teams.

You will contribute to improving processes, ensuring product quality, and supporting regulatory inspections with careful documentation and training development.

Qualifikationen

  • Completed vocational training as pharmaceutically-technical or chemically-technical assistant (m/w/d) or equivalent education/ studies.
  • Experience in a chemical, pharma or food production environment.
  • Strong technical understanding of production processes.
  • High quality consciousness and sense of responsibility.
  • Communicative and goal-oriented personality.
  • Excellent German and good English skills (spoken and written).
  • SAP and MS-Office skills complement your profile.

Aufgaben

  • Open and process non-conformances; investigate root causes.
  • Define corrective actions and CAPAs with cross-function teams.
  • Update SOPs, WIs, MBRs, FRMs as needed.
  • Create trainings to prevent deviations and support inspections.

Kenntnisse

Agile Manufacturing
Analytics Dashboards
Chemistry
Manufacturing
Data Compilation
Data Savvy
Execution Focus
Gap Analysis
GMP
Issue Escalation
Operational Excellence
Pharmaceutical Industry
Plant Operations
Proactive Behavior
Problem Solving
Process Optimization
Project Administration
Quality Auditing

Ausbildung

Pharmaceutical-technical or chemical-technical training or equivalent

Tools

SAP
MS-Office

Jobbeschreibung

Johnson & Johnson via Cilag AG seeks an Operations Specialist - Non-Conformances Coordinator at the Schaffhausen site to manage deviations, drive root-cause analysis, and implement CAPAs in close collaboration with QA and manufacturing teams.

You will contribute to improving processes, ensuring product quality, and supporting regulatory inspections with careful documentation and training development.

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