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Bioprocess Engineer

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there is no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that is the kind of work we want to be part of.Our Bioprocess Engineer USP will take over and manage the operational activities of assigned manufacturing projects with overall responsibility of standardization equipment/systems at Up Stream- (USP) within the Business Unit, Manufacturing Complex 2 (6x20kL Large Scale Mammalian). Key responsibilities:Develop and implement MC2 standardization equipment strategy and roadmap in alignment with local (site Visp) and global Lonza SU strategy.Lead multi-disciplinary project teams as functional lead for all manufacturing aspects of assigned projects.Ensure a high level of technical and process standardization within the production plant.Work as production expert in capital investment projects for building and commissioning of manufacturing units.Implement state of the art GMP documents and regulatory requirements for corresponding SU assets and products. Key requirements:BSC/MSc plus respectively > 5/3 years’ experience within the biotechnology industry.Excellent biotechnology expertise and/or knowledge in biotechnical engineering preferable in the area of mammalian cell culture and primary capture operations.Practical experience with stainless steel and Single Use Systems.Strong leadership and very good communication skills through interaction with all kinds of interfaces within and outside the organization; strong team orientation. Structured problem solving skills (Lean Six Sigma Yellow / Green Belt), focused and well-organized working attitude; open-minded for new ideas and suggestions; high motivation and dynamic drive; solution-oriented.Expert Delta V and/or Syncade Emerson systems.Deviation / investigations including RCAChange ManagementFluent in German and/or English; advanced GMP understanding.Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Bioprocess Engineer USP (80-100%)

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. 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 cultureAn inclusive and ethical workplaceCompensation programs that recognize high performanceIn addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. The full list of our local tailored benefits can also be found below.Benefits in Visp: https://bit.ly/3wjkoFi What you will do:Plan, execute, and document manufacturing campaigns for mammalian cell culture and purification processes.Lead cross-functional project teams as Functional Lead for all manufacturing-related aspects of assigned products.Prepare and manage SHE (Safety, Health & Environment), Environmental Monitoring, operational, and cleaning risk assessments, ensuring implementation of mitigation measures.Create, maintain, and implement GMP-compliant production documentation and ensure compliance with current regulatory requirements.Oversee manufacturing activities according to cGMP standards, including batch execution, deviation management, troubleshooting, and process optimization.Act as the manufacturing expert in capital investment projects, supporting design, commissioning, qualification, and automation of production facilities and equipment.Train biotechnologists/operators, support customer audits and inspections, and drive continuous improvement, innovation, and standardization initiatives within the production plant. What we are looking for:BSC/MSc plus respectively > 3/2 years’ experience within the biotechnology industry.Strong biotechnology expertise and/or knowledge in biotechnical engineering preferable in the area of mammalian cell culture and primary capture operations.Practical experience with stainless steel and Single Use Systems.Good communication skills through interaction with all kinds of interfaces within and outside the organization; strong team orientation.Structured problem solving skills (Lean Six Sigma Yellow / Green Belt), focused and well-organized working attitude; open-minded for new ideas and suggestions; high motivation and dynamic drive; solution-oriented.Knowledge Delta V and/or Syncade Emerson systems isGMP understanding: Deviation / investigations including RCA, Change ManagementFluent in English; knowledge in German is a plus 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. Ready to shape the future of life sciences? Apply now.

Senior QA Specialist, Bioconjugates 80-100% (f/m/d)

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.The site in Visp, Switzerland is growing and for our Biologics Quality organization, we are currently looking for a Senior QA Specialist (f/m/d) for the Bioconjugates plant. The successful candidate will be responsible for QA Bioconjugates activities and will be in direct contact with the key stakeholders in the Operations Team, MSAT, QA/QC & Project Management teams within the organization.What you will get: An agile career and dynamic working cultureAn inclusive and ethical workplaceCompensation programs that recognize high performanceA variety of benefits dependant on role and locationThe full list of our global benefits can be also found on https://www.lonza.com/careers/benefits.What you will do:Support continuous improvement programs to establish effective Quality Management System in Bioconjugates.Partner closely with cross‑functional teams to identify risks, drive deviation management & continuous improvement.Guide and influence stakeholders by providing QA expertise, ensuring robust quality culture and operational compliance.Manage and actively participate in “QA on the floor” program, including QA walkdowns and GEMBA walks. Act as QA SME in meetings with the relevant stakeholders, and customers, in audits and inspections.Responsible for the review and final release of records like Standard Operating Procedures (SOPs), Deviations, Change Requests, Effectiveness Checks, risk assessment etc.Identify emerging QA relevant topics, communicating to the relevant stakeholders and working actively on their development into new or already established Quality and Compliance strategies and/or standards i.e., CAPAs.Train and coach new employees and existing QA Specialists.What we are looking for: Academic degree in Chemistry/ Biotechnology/ Life Science or related field.Extensive experience in the GMP-regulated pharmaceutical industry including continuous improvement within QA area required.Green Belt certification is an advantage.General knowledge of manufacturing processes, great understanding and knowledge in Deviations, CAPA and  Change Request management including related activities.Demonstrated ability to act proactively with a detail‑oriented, problem‑solving and continuous‑improvement mindset.Write, review and approve documents e.g. SOPs and other Quality documents as applicableExperience in the interaction with health authorities (Swissmedic, FDA etc.) is desired.We are looking for someone who is independent, sociable, pro-active, customer focused and who values working as a team player.Experience as a QA trainer or trained as a trainer for Quality topics is an advantage.Experience with TrackWise, SAP, and Microsoft Office software is preferred.Fluency in English is required; German would be an asset.About LonzaAt 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.Ready to shape the future of life sciences? Apply now.

Bioprocess Engineer (m/w/d) 80%-100%

Bioprocess Engineer (m/f/d) 80%-100%The actual location of this position is Visp, Switzerland. Relocation support is available for eligible candidates and their families if required.As a Bioprocess Engineer, you will play a key role in the planning, execution, and continuous improvement of our GMP bioprocesses. Working closely with Operations, MSAT, Quality, and Engineering, you will help ensure reliable, efficient, and high-quality production, directly contributing to the manufacture of life-changing therapies for patients worldwide.This is a fully site-based position. Close in-person collaboration enables real-time alignment and supports the technical precision required to manufacture medicines to the highest quality and safety standards. Remote work is not available for this role.What you will get:An agile career path and a dynamic working culture.An inclusive and ethical work environment.Compensation programs that recognize high performance.The opportunity to actively shape and optimize complex GMP bioprocesses.Collaboration with cross-functional teams in an international environment.Diverse development and training opportunities.In addition to a competitive salary, we offer a wide range of benefits supporting lifestyle, family, and leisure activities. Our full list of local benefits can be found here: Benefits in Visp: https://bit.ly/3wjkoFiWhat you will do:Plan, execute, and document GMP manufacturing campaigns in close collaboration with the Head of Operations.Provide technical and organizational support for GMP production, including training and coaching production personnel.Create, optimize, and review GMP-related production documentation such as EBRs, SOPs, and work instructions.Ensure high-quality and timely handling of deviations, change controls, and CAPAs following a first-time-right approach.Monitor, analyze, and report operational process KPIs and identify and implement improvements using Lean, Six Sigma, and Kaizen methodologies.Ensure production equipment and manufacturing areas remain in a qualified and technically compliant state; perform troubleshooting and participate in on-call duty rotations.Execute and optimize cleaning processes and perform risk assessments related to SHE, Operations, Environmental Monitoring, and Cleaning Validation.What we are looking for:Bachelor's or Master's degree in Biotechnology, Bioprocess Engineering, Chemical Engineering, Life Sciences, or a related scientific or technical discipline.Experience in a GMP-regulated environment within the biotechnology, pharmaceutical, or life sciences industry.Strong knowledge of biotechnological manufacturing processes, GMP requirements, and documentation standards.Experience with deviations, CAPAs, change controls, and risk assessments.Excellent analytical skills with a structured, solution-oriented approach and strong technical understanding.Experience with Operational Excellence, Lean Manufacturing, Six Sigma, or similar continuous improvement methodologies is considered an advantage.Excellent English language skills and strong communication and teamwork abilities.About LonzaAt Lonza, our people are our greatest strength. Across more than 30 sites on 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. Every idea, whether big or small, has the potential to improve millions of lives, and we invite you to be part of that mission.Innovation thrives when people from diverse 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 are ready to transform our customers' groundbreaking ideas into viable therapies, we would be delighted to welcome you on board.Ready to shape the future of Life Sciences? Apply now!

Anlageningenieur Bioconjugates 80-100% (m/w/d)

Sofern erforderlich, steht berechtigten Kandidaten und ihren Familien Unterstützung beim Umzug zur Verfügung.Werde Teil unseres Engineering Teams als Anlageingenieur Bioconjugates 80-100% (m/w/d) in Visp und gestalte die Zukunft moderner Produktionsanlagen aktiv mit. Als Anlageingenieur Bioconjugates sorgst du für eine hohe Anlagenverfügbarkeit, treibst Optimierungen voran und leistest einen wichtigen Beitrag zu einem effizienten und zuverlässigen Betrieb.Was wir Dir bieten:Eine agile Karriere und eine dynamische ArbeitskulturEin integrativer und ethischer ArbeitsplatzVergütungsprogramme, die hohe Leistung anerkennenNeben einem wettbewerbsfähigen Gehalt erwarten Sie zahlreiche Vorteile in den Bereichen Lifestyle, Familie und Freizeit. Die vollständige Liste unserer globalen Leistungen finden Sie auch unter: Benefits - VispDeine Aufgaben:Gewährleisten einer fachgerechten und wirtschaftlichen Durchführung der Instandhaltung bei gleichzeitig ausreichender Anlagenverfügbarkeit, inkl. Umgang mit den BehördenVorbereitung und Koordination der Instandhaltungsarbeiten gemeinsam mit den WerkstättenLaufenden Optimierung von Prozessen, Anlagen und internen Abläufen im VerantwortungsbereichArbeiten mit SAP (Auftragserteilung, technisch- kommerzielle Auswertungen, Kapazitätsplanung zur Optimierung von Anlagen- und Personaleinsatz, etc.)Mitarbeit bei der Überwachung und Einhaltung des zur Verfügung stehenden Budgets (Unterhalt, Umstellungen und Investitionen) im VerantwortungsbereichSicherstellen, Aktualisieren und Überprüfen der laufenden Anlagendokumentation, z.B. Fliessbilder, Zonen- und Aufstellungspläne, Stücklisten, Änderungswesen nach GMPStellvertretungen und Dienste innerhalb der Abteilung, technische Projektleitung oder Mitarbeit in Teil- und Kleinprojekten, z. B. verfahrenstechnische Berechnungen und Optimierungen in der Anlage; Machbarkeitsstudien Neuanlagen und/ oder Umbau bestehender Anlagen inkl. Kostenabschätzung, Termine und Funktionalität; Risikoanalysen, Betriebsversuchen und UmstellungenAusbildung der Anlagen-Mannschaft und des Werkstattpersonals bezüglich Prozess- und Anlagenkenntnissen sowie betreffend Sicherheit, Hygiene, Umwelt und Qualität (cGMP)Dein Anforderungsprofil:Technikerschule (HF) / Fachhochschule (FH) / Uni Studium (Maschinenbau, Verfahrenstechnik)Fundierte Berufserfahrung in Engineering und Maintenance wünschenswertKenntnisse in MS-Office und SAP Strukturierter, lösungsorientierter und sehr organsierter ArbeitsstilFliessende Deutsch- und gute EnglischkenntnisseÜber Lonza:Bei Lonza sind unsere Mitarbeiter unsere größte Stärke. An über 30 Standorten auf fünf Kontinenten arbeiten unsere global vernetzten Teams täglich zusammen, um die Medikamente von morgen herzustellen. Unsere Grundwerte: Zusammenarbeit, Verantwortlichkeit, Exzellenz, Leidenschaft und Integrität spiegeln wider, wer wir sind und wie wir zusammenarbeiten. Die Ideen jedes Einzelnen, ob groß oder klein, haben das Potenzial, Millionen von Leben zu verbessern, und genau daran möchten wir Dich teilhaben lassen.Innovation gedeiht, wenn Menschen unterschiedlichster Herkunft ihre einzigartigen Perspektiven einbringen. Bei Lonza schätzen wir Vielfalt und setzen uns für ein integratives Umfeld für alle Mitarbeiter ein. Wenn Du bereit bist, die bahnbrechenden Ideen unserer Kunden in praktikable Therapien umzusetzen, freuen wir uns, Dich an Bord begrüßen zu dürfen.Bereit die Zukunft der Life Sciences zu gestalten? Jetzt bewerben

Bioprocess Engineer for MMM MC1 DSP 80-100% (m/f/d)

Relocation assistance is available for eligible candidates and their families, if needed. Join our Bioprocess DSP Team in Visp as Bioprocess Engineer for MMM MC1 DSP 80-100% (m/f/d) and be part of a world‑class environment where innovation meets purpose. You’ll play a key role in purifying life‑saving therapies while collaborating with talented experts in a dynamic, high-performance setting. If you’re passionate about biotechnology and want to make a real impact, this is your opportunity.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’ll get:An agile career and dynamic working cultureAn inclusive and ethical workplaceCompensation programs that recognize high performanceIn addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. What you’ll do:Serve as the Bioprocess Engineer (BPE) for DSP manufacturing operations, ensuring reliable execution of clinical and commercial manufacturing campaigns within safety, quality, and GMP requirements.Act as the primary MES and manufacturing systems representative for the assigned DSP area, supporting recipe execution, troubleshooting, optimization, and continuous improvement activities.Provide first-line support for DeltaV and Manufacturing Execution Systems (MES), working closely with Operations, Automation, MSAT, QA, and Technical Support Teams  to resolve process and system issues.Own, maintain and review electronic Batch Records (eBRs), manufacturing recipes, workflows, and associated GMP documentation to ensure compliance, data integrity, and operational efficiency.Lead investigations, deviations, CAPAs, and change controls related to manufacturing systems, batch execution, and process documentation.Drive digitalization and process improvement initiatives by identifying opportunities to simplify workflows, enhance data visibility, and improve manufacturing performance.Support process transfers, new product introductions, validation activities, and implementation of manufacturing system enhancements.Act as a key interface between Production, Automation, MSAT, QA, and Technical Services to ensure robust and compliant manufacturing operations.What we are looking for:Master's Degree in Biotechnology, (Bio)chemical Engineering, Life Sciences, Automation, Industrial Engineering, or a related discipline; alternatively, a Bachelor's Degree with relevant biopharmaceutical manufacturing experience.Experience in biopharmaceutical manufacturing with strong understanding of DSP processes and GMP requirements.Knowledge of Manufacturing Execution Systems (MES), electronic Batch Records (eBR), and process automation platforms such as DeltaV.Experience supporting manufacturing operations, troubleshooting process and system-related issues, and driving continuous improvement initiatives.Understanding of data integrity principles, change management, deviation management, and GMP documentation requirements.Strong analytical and problem-solving skills with the ability to manage multiple stakeholders across Operations, QA, Automation, MSAT, and Technical Services.Excellent communication skills in English; German language skills are considered an advantage.Ability to work in a fast-paced manufacturing environment while maintaining a strong focus on quality, compliance, and operational excellence.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. 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.Ready to shape the future of life sciences? Apply now.

Manager, QA, Data Integrity Program Manager

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.You will support the site's Data Integrity (DI) program at one of the largest biologics manufacturing sites in the world, where reliable, complete, and accurate data is essential to ensuring product quality, patient safety, regulatory compliance, and operational excellence.In this role, you will work closely with the Site Data Integrity Lead and cross-functional stakeholders to support Data Integrity governance, promote ALCOA+ principles, support continuous improvement activities, and help maintain a sustainable state of compliance across the Visp site.What you will get• A place in an inclusive, dynamic, and passionate team, with the opportunity to contribute to the site's Data Integrity program and collaborate with cross-functional stakeholders across a diverse GMP manufacturing environment.• An agile career and a dynamic work culture.• An inclusive and ethical workplace.• Compensation programs that recognize high performance.What you will do• Support the site's Data Integrity governance program and contribute to the implementation of DI standards, initiatives, and site-specific improvement activities. • Promote Data Integrity awareness and ALCOA+ principles through training programs, coaching, and engagement with site functions across Visp. • Plan, coordinate, and support the execution of Data Integrity Walkthroughs across the Visp site and drive follow-up actions as required. • Support and coordinate Data Integrity assessments, remediation activities, and continuous improvement initiatives across GMP processes on site. • Provide Data Integrity support for deviations, investigations, change controls, CAPAs, quality risk assessments, audits, and inspections. • Deputize the Visp Data Integrity Community and act as deputy for the Site Data Integrity Lead, facilitating community meetings, stakeholder engagement, and site-wide alignment activities as required.What we are looking for• Academic degree in Life Sciences, Engineering, Information Technology, Pharmaceutical Sciences, Quality Management, or another relevant discipline.• Experience in a GMP-regulated pharmaceutical, biotechnology, or healthcare environment.• Good understanding of Data Integrity principles, ALCOA+, computerized systems, and applicable regulatory requirements.• Experience with quality processes, including deviations, investigations, CAPAs, change controls, and risk assessments.• Ability to identify compliance risks, evaluate issues, and support the implementation of effective and pragmatic solutions.• Strong communication and collaboration skills with the ability to work effectively in cross-functional teams.• Experience supporting Data Integrity, compliance, computerized systems, CSV, Quality Systems, or related GMP activities.• Experience supporting audits, inspections, or regulatory interactions is desirable.• Fluency in English is required; German is an advantage.

Automatisierungsingenieur / Automation Specialist 80–100 % (m/w/d)

Sofern erforderlich, steht berechtigten Kandidaten und ihren Familien Unterstützung beim Umzug zur Verfügung.Werde Teil unseres EMR-Teams in Visp!Zur Verstärkung unseres Engineering-&-Maintenance-Teams im Bereich Development & Manufacturing Solutions am Standort Visp suchen wir eine/n Elektro-, Mess- und Regeltechnik (EMR) Ingenieur/in. Die Position umfasst die Verantwortung für die Instandhaltung und verschiedene Projekte in Mono- oder Mehrprodukteanlagen.Was wir bieten:Eine agile Karriere und eine dynamische ArbeitskulturEin integrativer und ethischer ArbeitsplatzVergütungsprogramme, die hohe Leistung anerkennenNeben einem wettbewerbsfähigen Gehalt erwarten Dich zahlreiche Vorteile in den Bereichen Lifestyle, Familie und Freizeit. Die vollständige Liste unserer globalen Leistungen findest Du unter:Benefits - VispDeine Aufgaben:Planung und Durchführung von Investitions- und Umstellungsaufgaben in einem automatisierten Produktionsbetrieb für pharmazeutische WirkstoffeKontinuierliche Anpassung und Verbesserung von Anlagen, Prozessen und Produktwechseln mit Fokus auf Qualität, Sicherheit und LeistungSicherstellung des reibungslosen Betriebs und der zuverlässigen Performance hochautomatisierter Produktionsanlagen mit DeltaV- und MES-SystemenGMP-konforme Durchführung von Prüfungen, Dokumentationen und Änderungsmanagement unter Verwendung von Kneat und UbikErstellung und Pflege von Anlagendokumentationen in SAP/COMOS zur Sicherstellung regulatorischer AnforderungenKoordination und Überwachung von Projekten hinsichtlich Funktionalität, Leistung, Kosten und TerminenBegleitung der Projekte von der Planung bis zur erfolgreichen InbetriebnahmeEffiziente Planung und Organisation der Instandhaltung zur Sicherstellung von Anlagenverfügbarkeit und BetriebssicherheitFörderung technologischer Weiterentwicklungen durch eine innovative und proaktive ArbeitsweiseAktive Mitarbeit in fachübergreifenden GremienDein Profil:Abgeschlossenes Bachelor- oder Masterstudium in Elektro-, Automations- oder Systemtechnik bzw. InformatikErste Berufserfahrung im Betriebs- oder Projektengineering, in der Instandhaltung oder im Anlagenneubau, idealerweise in einem GMP-regulierten Umfeld der Pharma- oder ChemieindustrieKenntnisse in GMP, COMOS, DeltaV, MES und SAPFreude an interdisziplinärer Zusammenarbeit sowie eine selbstständige und flexible ArbeitsweiseAusgeprägte Teamfähigkeit und sehr gute KommunikationsfähigkeitenGute Deutsch- und Englischkenntnisse in Wort und SchriftGeschäftliches Denken, hohe Motivation und VeränderungsbereitschaftBei Lonza sind unsere Mitarbeiter unsere grösste Stärke. An über 30 Standorten auf fünf Kontinenten arbeiten unsere global vernetzten Teams täglich zusammen, um die Medikamente von morgen herzustellen. Unsere Grundwerte: Zusammenarbeit, Verantwortlichkeit, Exzellenz, Leidenschaft und Integrität spiegeln wider, wer wir sind und wie wir zusammenarbeiten. Die Ideen jedes Einzelnen, ob gross oder klein, haben das Potenzial, Millionen von Leben zu verbessern, und genau daran möchten wir Sie teilhaben lassen.Innovation gedeiht, wenn Menschen unterschiedlichster Herkunft ihre einzigartigen Perspektiven einbringen. Bei Lonza schätzen wir Vielfalt und setzen uns für ein integratives Umfeld für alle Mitarbeiter ein. Wenn Sie bereit sind, die bahnbrechenden Ideen unserer Kunden in praktikable Therapien umzusetzen, freuen wir uns, Sie an Bord begrüssen zu dürfen.Bereit die Zukunft der Life Sciences zu gestalten? Jetzt bewerben!