QA Manager — Lonza
- Località
- Visp
- Contratto
- full-time
- Pubblicato
- 4 giorni fa
Panoramica
The actual location of this job is in Stein, Switzerland.
Relocation assistance is available for eligible candidates and their families, if needed.
In order to support our business growth in Stein (Switzerland), we are looking for a Quality Assurance Manager with expertise in Drug Product systems qualification, QC analytical equipment qualification and CSV & Automation.
- The actual location of this job is in Stein, Switzerland.
- Relocation assistance is available for eligible candidates and their families, if needed.
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities What you’ll get: An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance What you will do:
Responsabilità principali
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities What you’ll get: An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance What you will do:
- Responsible for Equipment, QC, Computerized System Validation (CSV) and Automation deliverables for new aseptic facilities, equipment and utilities related to the GMP manufacturing of drug products
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
- Representing Quality in the CAPEX project organization in regards to Equipment, QC, Computerized System Validation (CSV) and Automation and Automation
- Reviewing and releasing quality related to Equipment, QC, Computerized System Validation (CSV) and Automation project deliverables
- Ensuring Equipment, QC, Computerized System Validation (CSV) and Automation deliverables meet Global procedures, regulatory requirements and policies
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders What we are looking for:
- Bachelor or Master degree in computer science, engineering, life science or related field
- Significant experience in the GMP regulated pharmaceutical industry project; preferable in a role within a Quality Unit
- Knowledgeable in commissioning and qualification of aseptic manufacturing systems and QC analytical systems, Annex 1 requirements
- Knowledgeable in CSV, Data Integrity, Automation systems and related Guidelines (21 CFR Part 11, EU GMP Annex 11, GAMP5 and the underlying principles of each)
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.) Sound knowledge of MES and DCS is required
- Fluency in English, German would be an advantage
Dettagli ulteriori
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders What we are looking for:
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.) Sound knowledge of MES and DCS is required
Note e contenuto originale
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities
- What you’ll get:
- An agile career and a dynamic work culture
- An inclusive and ethical workplace
- What you will do:
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders
- What we are looking for:
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.)
- Sound knowledge of MES and DCS is required
Domande frequenti su questo annuncio
Che stipendio offre Lonza per questa posizione?
Lonza indica CHF 85'500 - 129'500 lordi annui per questo ruolo a Visp. 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.
