Tirocinante - QA Specialista Batch Record Review — Lonza
- Località
- CH
- Contratto
- full-time
- Pubblicato
- 61 giorni fa
Panoramica
The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation.
This role provides hands‑on exposure to regulated industry practices, including data integrity, documentation control, and compliance with internal procedures and regulatory standards.
The intern will work closely with QA specialists and cross‑functional teams to ensure timely and accurate batch record processing.
Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get
- An agile career and a dynamic work culture.
- Compensation programs that recognize high performance.
What you will do
- Review of the Executed Batch Records (e.g.
cleaning logs, production documentation review, temperature reports, test procedures, raw data, logbooks)
- Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager
- Support the initiation of deviations and investigations for Batch Record review related observations What we are looking for:
- Bachelor degree or relevant work/ internship experience in Biology, Chemistry, Biotechnology, Life Science or other related field
- Previous experience in GMP regulated pharmaceutical / API industry is an advantage
- Ability to identify non-compliance and gaps from quality standards
- Structured, precise and well-organized working attitude; open-minded for new ideas and suggestions; agile, highly motivated and dynamic drive
- English: Fluent.
About Lonza At Lonza, our people are our greatest strength.
With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow.
Processo di candidatura
- now.
- Lonza is a global leader in pharma and biotech manufacturing.
- The company operates major production facilities in Visp (Valais), Basel, and Stein (Aargau), Switzerland.
Azienda e contesto
- The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation.
- This role provides hands‑on exposure to regulated industry practices, including data integrity, documentation control, and compliance with internal procedures and regulatory standards.
- The intern will work closely with QA specialists and cross‑functional teams to ensure timely and accurate batch record processing.
- This is a fully site‑based role.
- Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get:
- An agile career and a dynamic work culture.
- An inclusive and ethical workplace.
- Compensation programs that recognize high performance. What you will do:
- Review of the Executed Batch Records (e.g. cleaning logs, production documentation review, temperature reports, test procedures, raw data, logbooks)
- Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager
Dettagli ulteriori
- Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
- Compensation programs that recognize high performance.
Note e contenuto originale
- What you will get:
- What you will do:
Domande frequenti su questo annuncio
Che stipendio offre Lonza per questa posizione?
Lonza indica CHF 49'500 - 66'500 lordi annui per questo ruolo a CH. Questo è lo stipendio pubblicato nell'annuncio originale (o, quando il datore non specifica una cifra, una stima realistica per ruolo e settore) — il calcolatore di questo sito lo converte nel netto reale una volta applicate imposta da frontaliere e contributi sociali.
È un ruolo a tempo pieno, e che tipo di contratto offre Lonza?
Questo annuncio è una posizione a tempo pieno. Il tipo di contratto mostrato qui arriva direttamente dall'annuncio originale del datore di lavoro; conferma sempre orario esatto, preavviso e durata del periodo di prova con Lonza durante il colloquio, perché questi dettagli possono variare anche all'interno della stessa categoria contrattuale.
Serve un permesso da frontaliere per un ruolo nel canton Vallese?
I residenti UE/AELS nella zona di frontiera del paese confinante con il canton Vallese possono richiedere il Permesso G; il datore di lavoro svizzero lo presenta all'ufficio della migrazione di quel canton dopo la firma del contratto. Regole sulla zona di frontiera e tempi di lavorazione variano per paese confinante e canton — verifica i dettagli con l'ufficio della migrazione del canton Vallese o con HR durante il colloquio.
Come mi candido a questa posizione presso Lonza?
Usa il pulsante "Candidati ora" in questa pagina — rimanda direttamente all'annuncio originale di Lonza su lonza.wd3.myworkdayjobs.com, quindi la tua candidatura arriva direttamente nel sistema di gestione candidature del datore di lavoro. Frontaliere Ticino non raccoglie né inoltra candidature in proprio.
