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NONovartis Radiopharmaceuticals GmbH

Process Expert(m/w/x)

Halle (Saale)
Vollzeitmit HomeofficeBerufserfahren

Front-line manufacturing support for compliant batch production at a global pharmaceutical company, driving root cause investigations. 3 years' experience in GMP manufacturing process support or QA/QC shop floor role required. Specific disability support available.

Anforderungen

  • Bachelor's degree in engineering, Pharmacy, Pharmaceutical Technology, Chemistry, or relevant experience
  • 3 years' experience in process support shop floor role in GMP manufacturing and/or QA/QC
  • Proven process understanding (Pharma, GMP, Regulatory aspects)
  • Strong awareness of quality issues
  • Compliance investigations experience
  • Excellent technical writing skills
  • Fluency in German and English
  • Previous Radiopharma experience (a plus)
  • Prior leadership and/or high cross-functional experience (preferred)

Aufgaben

  • Provide front-line manufacturing support.
  • Ensure safe and compliant batch manufacturing.
  • Act as Subject Matter Expert (SME).
  • Serve as first point of contact for product and process issues.
  • Drive investigations to root cause.
  • Implement corrective and preventive actions (CAPAs).
  • Manage and maintain Master Batch Records.
  • Manage and maintain Standard Operating Procedures (SOPs).
  • Manage and maintain risk assessments and protocols.
  • Write and review SOPs, batch records, and white papers.
  • Collect data for ongoing process verification (OPV).
  • Track and evaluate product performance.
  • Support CAPA implementation.
  • Author and own material transfer investigations.
  • Author and own API synthesis investigations.
  • Author and own Drug Substance formulation investigations.
  • Author and own Drug product filling investigations.
  • Author and own inspection and packaging investigations.
  • Ensure processes are inspection-ready.
  • Support process optimization and new technology introduction.
  • Review validation protocols and reports.
  • Support execution of process validations.
  • Support short-term improvement projects.
  • Guide and support production teams.
  • Train and share knowledge with production teams.
  • Guide processes to closure and completion.

Berufserfahrung

  • 3 Jahre

Ausbildung

  • Bachelor-Abschluss

Sprachen

  • Deutschverhandlungssicher
  • Englischverhandlungssicher

Benefits

Sonstige Vorteile

  • Disability support
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Novartis Radiopharmaceuticals GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.

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