Bioprocess Ingénieur DSP — Lonza
- Lieu
- Visp
- Contrat
- full-time
- Publié
- Hier
Vue d’ensemble du poste
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.
Ce que l’entreprise offre
- 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.
Processus de candidature
- 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.
Entreprise et contexte
- 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.
Détails supplémentaires
- 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:
Notes et contenu original
- 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:
Questions sur cette offre
Quel salaire propose Lonza pour ce poste ?
Lonza indique CHF 68 000 - 92 000 bruts par an pour ce poste à Visp. Il s'agit du salaire publié dans l'annonce d'origine (ou, si l'employeur ne précise pas de montant, d'une estimation réaliste pour le rôle et le secteur) — le calculateur de ce site le convertit en net réel une fois l'impôt frontalier et les cotisations sociales appliqués.
Est-ce un poste à temps plein, et quel type de contrat propose Lonza ?
Cette offre est un poste en temps plein. Le type de contrat affiché ici provient directement de l'annonce originale de l'employeur ; confirmez toujours les horaires exacts, le préavis et la durée d'essai avec Lonza pendant le processus de candidature, ces détails pouvant varier même au sein de la même catégorie de contrat.
Ai-je besoin d'un permis de frontalier pour un poste dans le canton de Valais ?
Les résidents UE/AELE domiciliés dans la zone frontalière du pays voisin du canton de Valais peuvent demander un permis G ; l'employeur suisse le dépose auprès de l'office cantonal des migrations après signature du contrat. Les règles de zone frontalière et les délais varient selon le pays voisin et le canton — confirmez les détails auprès de l'office des migrations du canton de Valais ou avec les RH pendant la candidature.
Comment postuler à ce poste chez Lonza ?
Utilisez le bouton « Postuler maintenant » sur cette page — il renvoie directement à l'annonce originale de Lonza sur lonza.wd3.myworkdayjobs.com, votre candidature arrive donc directement dans le système de suivi des candidatures de l'employeur. Frontaliere Ticino ne collecte ni ne transmet lui-même les candidatures.
