Bioprocess Ingenieur DSP — Lonza
- Ort
- Visp
- Vertrag
- full-time
- Veröffentlicht
- Gestern
Rollenüberblick
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.
Was das Unternehmen bietet
- 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.
Bewerbungsprozess
- 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.
Unternehmen und Kontext
- 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.
Weitere Details
- 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:
Notizen und Originalinhalt
- 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:
Fragen zu dieser Stellenanzeige
Welches Gehalt bietet Lonza für diese Stelle?
Lonza gibt CHF 68'000 - 92'000 brutto pro Jahr für diese Position in Visp an. Dies ist das im Original-Inserat veröffentlichte Gehalt (oder, falls der Arbeitgeber keinen Betrag nennt, eine realistische Schätzung für Rolle und Branche) — der Rechner auf dieser Seite berechnet daraus Ihr tatsächliches Netto nach Grenzgänger-Steuer und Sozialabgaben.
Ist das eine Vollzeitstelle, und welchen Vertragstyp bietet Lonza?
Diese Stelle ist eine Vollzeit-Position. Der hier angezeigte Vertragstyp stammt direkt aus dem Original-Inserat des Arbeitgebers; klären Sie genaue Arbeitszeiten, Kündigungsfrist und Probezeit während des Bewerbungsprozesses mit Lonza, da diese Details auch innerhalb derselben Vertragskategorie variieren können.
Brauche ich eine Grenzgänger-Bewilligung für eine Stelle im Kanton Wallis?
EU/EFTA-Bürger mit Wohnsitz in der Grenzzone des an den Kanton Wallis angrenzenden Landes können eine G-Bewilligung beantragen; der Schweizer Arbeitgeber reicht sie nach Vertragsunterzeichnung beim Migrationsamt dieses Kantons ein. Grenzzonen-Regeln und Bearbeitungszeiten variieren je nach Nachbarland und Kanton — klären Sie die Details mit dem Migrationsamt des Kantons Wallis oder mit HR während der Bewerbung.
Wie bewerbe ich mich für diese Stelle bei Lonza?
Nutzen Sie die Schaltfläche "Jetzt bewerben" auf dieser Seite — sie führt direkt zum Original-Inserat von Lonza unter lonza.wd3.myworkdayjobs.com, sodass Ihre Bewerbung direkt im Bewerbermanagementsystem des Arbeitgebers landet. Frontaliere Ticino sammelt oder leitet keine Bewerbungen selbst weiter.
