Batch Record Reviewer

vor 2 Wochen


Visp, Schweiz BioTalent Vollzeit CHF 60'000 - CHF 80'000 pro Jahr

Deutsch
12-Monats-Vertrag: Batch Record Reviewer (m/w/d)
Standort: [Ort einfügen]

Wir suchen eine engagierte Person, die als Batch Record Reviewer eigenverantwortlich Produktions- und Reinigungsprotokolle im pharmazeutischen Umfeld überprüft und Daten in Kontrollsysteme überträgt. Sie arbeiten eng mit QA und Betrieb zusammen und nehmen an Review-Meetings teil. Zudem leisten Sie bei Bedarf Unterstützung bei allgemeinen Betriebseinheiten wie Präsentationserstellung, Büro-materialbestellungen oder Dokumentenarchivierung.

Ihre Aufgaben:

  • Selbstständige und termingerechte Prüfung von Herstell- und Reinigungsdokumenten gemäß interner Arbeitsanweisung

  • Pflege der Dokumenten- und KPI-Listen sowie Unterstützung des Anlageteams

  • Dokumentensupport für Projektteams (z. B. Bereitstellung/Einsammlung, Etikettenkontrolle)

  • Erstellung des Produktionsnachweises nach Abschluss eines Batches

  • Verantwortung für die Archivierung prozess­relevanter Dokumente

Ihr Profil:

  • Berufsausbildung und Erfahrung im pharmazeutischen Umfeld

  • Sehr gute Deutschkenntnisse in Wort und Schrift, Englisch von Vorteil

  • Verständnis der gültigen cGMP-Vorschriften

  • Gute IT-Kenntnisse (insbesondere MS Office)

  • Sorgfältige und strukturierte Arbeitsweise, Organisationstalent

  • Flexibilität, Kommunikationsstärke und Teamfähigkeit

Wenn Sie Lust haben, in einem dynamischen Umfeld Verantwortung zu übernehmen, freuen wir uns auf Ihre Bewerbung

English
12-Month Contract: Batch Record Reviewer (m/f/d)
Location: [insert location]

We are seeking a motivated professional to join us as a Batch Record Reviewer. In this role, you will independently review production and cleaning documents within a pharmaceutical environment, transfer data into control systems, and collaborate closely with QA and operations. You will also support general operational tasks when required, such as preparing presentations, ordering office supplies, and archiving documents.

Your Responsibilities:

  • Conduct timely and independent review of manufacturing and cleaning records according to internal procedures

  • Maintain document and KPI lists, supporting the plant team

  • Provide document support for project teams (e.g. distributing/collecting documents, label checks)

  • Create the production certificate upon batch completion

  • Manage the archiving of process-relevant documentation

Your Profile:

  • Professional qualification and experience in a pharmaceutical environment

  • Excellent German language skills (written & spoken), English is an advantage

  • Understanding of current cGMP regulations

  • Strong IT skills, especially in MS Office

  • Precise and structured work style, ability to organise daily tasks and meet deadlines

  • Flexible, communicative and a team player


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