Bioprocess Ingegnere DSP — Lonza
- Località
- Visp
- Contratto
- full-time
- Pubblicato
- Ieri
Panoramica
The actual location of this job is in Visp, Switzerland.
Relocation assistance is available for eligible candidates and their families, if needed.
This is a fully site‑based role.
- The actual location of this job is in Visp, Switzerland.
- Relocation assistance is available for eligible candidates and their families, if needed.
- in Visp: https://bit.ly/3wjkoFi
- The DSP Bioprocess Engineer is responsible for the planning, execution, monitoring, and documentation of commercial and clinical manufacturing campaigns within the Downstream Processing (DSP) area.
Cosa offre l’azienda
- in Visp: https://bit.ly/3wjkoFi
- The DSP Bioprocess Engineer is responsible for the planning, execution, monitoring, and documentation of commercial and clinical manufacturing campaigns within the Downstream Processing (DSP) area.
- The role serves as the manufacturing subject matter expert for assigned products, ensuring compliant, safe, efficient, and reliable production according to cGMP requirements, regulatory expectations, and operational excellence standards.
- The DSP Bioprocess Engineer acts as the Functional Lead for manufacturing-related activities, supports plant operations, leads risk assessments and process improvements, and provides technical expertise for capital projects, commissioning, qualification, and operational readiness. What you will do:
- Lead and oversee DSP manufacturing campaigns, ensuring execution, monitoring, troubleshooting, and documentation are compliant with cGMP and regulatory requirements.
- Act as the manufacturing Functional Lead for assigned products, coordinating cross-functional teams and maintaining technical expertise in processes, equipment, and facilities.
- Drive risk management activities, including SHE, EM, operational, cleaning, and product risk assessments, while supporting investigations, deviations, CAPAs, and change controls.
- Maintain GMP documentation such as SOPs, manufacturing instructions, risk assessments, and records to ensure compliance and audit readiness.
- Train and support manufacturing personnel, contributing to workforce development and fostering a culture of safety, quality, operational excellence, and continuous improvement.
- Represent manufacturing in capital projects, providing technical input for facility design, equipment selection, commissioning, qualification, and technology transfers.
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
- Strong communication and stakeholder management capabilities, enabling effective collaboration across functions and organizational levels.
- Demonstrated project leadership and team coordination experience within complex, regulated manufacturing environments.
- Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or a related field, along with relevant experience in biopharmaceutical manufacturing, process engineering, technical operations, or cGMP-regulated environments.
- 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.
- Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together.
- Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
- Innovation thrives when people from all backgrounds bring their unique perspectives to the table.
- At Lonza, we value diversity and are committed to creating an inclusive environment for all employees.
- If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
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. An agile career and a dynamic work culture An inclusive and ethical workplace
- Benefits in Visp: https://bit.ly/3wjkoFi
- The DSP Bioprocess Engineer acts as the Functional Lead for manufacturing-related activities, supports plant operations, leads risk assessments and process improvements, and provides technical expertise for capital projects, commissioning, qualification, and operational readiness.
- Lead continuous improvement initiatives and serve as a manufacturing representative during customer audits, inspections, and strategic cross-functional projects. What we are looking for:
Note e contenuto originale
- 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’ll get:
- An agile career and a dynamic work culture
- An inclusive and ethical workplace
- What you will do:
- Lead continuous improvement initiatives and serve as a manufacturing representative during customer audits, inspections, and strategic cross-functional projects.
- What we are looking for:
Domande frequenti su questo annuncio
Che stipendio offre Lonza per questa posizione?
Lonza indica CHF 68'000 - 92'000 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.
