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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.

Visp

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.

Visp

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.

Visp

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!

Visp

AI Products Lead

Location: Basel, Switzerland | Hybrid Relocation assistance is available for eligible candidates and their families, if needed. We are seeking an experienced AI Products Lead to drive Lonza's AI product portfolio across the value chain. In this strategic role, you will work closely with business and functional leaders to identify, shape, build, and scale AI products that deliver measurable business outcomes. You will own the product lifecycle from opportunity identification and prioritization through delivery, adoption, scaling, and retirement, partnering with the AI Factory, technology teams, and business stakeholders to maximize value creation. This role is primarily based on site. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20% of your time. Requests are considered on a case‑by‑case basis, in line with business needs. What you will get: An agile career and dynamic working culture.An inclusive and ethical workplace.Compensation programs that recognize high performance.A variety of benefits dependent on role and location. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below. Benefits in Basel: https://media.ffycdn.net/eu/lonza-group-ag/d/5c78e3b906804b0cb6710009ab5507de?updated What you'll do: Partner with business and functional leaders to identify, evaluate, and prioritize high-value AI opportunities that deliver measurable business impact.Own the end-to-end AI product lifecycle, including strategy, roadmap development, prioritization, delivery, adoption, scaling, and retirement.Translate business challenges into scalable AI products and use cases that enhance efficiency, innovation, and decision-making.Lead cross-functional collaboration between business stakeholders, AI specialists, data teams, IT, and external partners to ensure successful product delivery.Establish product management best practices, including governance, success metrics, value realization tracking, and portfolio management.Drive user adoption and change management activities to maximize the value and scalability of AI solutions across the organization.Ensure AI products comply with responsible AI principles, data governance requirements, security standards, and regulatory expectations. What we're looking for: Master's degree in Business Strategy, Artificial Intelligence, Data Science, Computer Science, or a related field.Significant experience in AI product management, digital product leadership, or technology-driven business transformation within complex organizations.Proven ability to take AI products from concept to implementation, driving adoption, scalability, and measurable business value.Strong understanding of AI, Generative AI, product lifecycle management, agile methodologies, and portfolio prioritization.Experience working across business, data, technology, and engineering teams, with excellent stakeholder management and influencing skills.Knowledge of AI governance, responsible AI principles, data management, security, and compliance requirements.Experience in life sciences, pharmaceuticals, manufacturing, CDMO, or other highly regulated industries is highly desirable. 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!

Basel

AI Strategy & Portfolio Lead

Location: Basel, Switzerland | Hybrid Relocation assistance is available for eligible candidates and their families, if needed. We are seeking an experienced AI Strategy & Portfolio Leader to define and drive Lonza's enterprise AI strategy, roadmap, and investment portfolio. In this highly visible role, you will partner with business leaders and key functions to translate strategic priorities into impactful AI initiatives, investment decisions, and measurable business outcomes. You will oversee the end-to-end AI portfolio lifecycle, from opportunity intake and prioritization through governance and value realization, while providing senior leadership with strategic insights on AI opportunities, risks, investments, and trade-offs. This role is primarily based on site. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20% of your time. Requests are considered on a case‑by‑case basis, in line with business needs. What you will get: An agile career and dynamic working culture.An inclusive and ethical workplace.Compensation programs that recognize high performance.A variety of benefits dependent on role and location. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below. Benefits in Basel: https://media.ffycdn.net/eu/lonza-group-ag/d/5c78e3b906804b0cb6710009ab5507de?updated What you'll do: Own and drive Lonza’s enterprise AI strategy, portfolio, and roadmap, ensuring alignment with business priorities and long-term objectives.Translate business goals into clear AI investment priorities, initiatives, and execution plans that deliver measurable value.Lead portfolio prioritization, investment governance, and value realization activities across AI programs and products.Partner closely with business leaders, Finance, GIA, and IT to identify high-impact opportunities and scale successful AI initiatives.Establish frameworks, metrics, and governance processes to track performance, business outcomes, and return on investment.Provide strategic recommendations on which initiatives to accelerate, optimize, pause, or discontinue based on value and organizational priorities.Bridge strategy and execution by driving decision-making, stakeholder alignment, and successful implementation across functions. What we're looking for: 10+ years of experience in strategy, AI strategy, digital transformation, portfolio management, technology strategy, or a related field.Proven track record of translating strategic priorities into investment decisions, portfolios, and measurable business outcomes.Strong experience engaging and influencing senior business stakeholders in complex, global organizations.Solid understanding of AI and emerging technologies, with the ability to translate technology trends into practical business opportunities.Strong commercial, financial, and value-driven mindset, including experience evaluating investments and business cases.Experience operating in matrix organizations, influencing without direct authority, and driving cross-functional alignment.Experience in pharmaceuticals, life sciences, CDMO, or other highly regulated industries is strongly preferred. 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!

Basel

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

Visp

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.

Visp

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.

Visp

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!

Visp

Customer Portal Product Owner and Data Governance Lead (m/w/d) (80-100%)

A Career at Lonza What you’ll getAn 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.Relocation support for eligible candidate Lonza is establishing a One Lonza customer portal and experience capability as a core workstream of the Data-as-a-Product initiative under the One Lonza Program Advanced Industry. The role is based in Basel, Switzerland We are actively looking for a driven Customer Portal and Experience Product Owner (Director level) to be accountable for shaping and delivering the customer-facing experience layer through which customers collaborate with Lonza and securely access documents, governed data products, insights and digital services. In this role you will own the workstream vision, customer journeys, product roadmap, requirements, operating model, governance, business case and implementation outcomes, while ensuring alignment with Data-as-a-Product strategy, business-platform roadmaps and Lonza’s broader digital architecture. Working across Commercial, Project Management, Operations, Quality, IT, Data, Security, Legal and external delivery partners, the role will create a scalable, secure and consistent experience across business platforms rather than a collection of disconnected portal solutions. What you will do Lead the Customer Portal Workstream: Lead the end-to-end Customer Portal and Experience workstream from strategy through execution, translating it into an executable product strategy, prioritized roadmap, milestones and measurable outcomes. Own Customer Experience and Product Direction: Define the target customer experience, personas, end-to-end customer journeys, design principles and value proposition across the customer lifecycle.Define Functional and Integration Requirements: Own the business and product requirements for information architecture, document and data exchange, collaboration workflows, dashboards, notifications, support services, APIs and integration with relevant enterprise systems. Shape MVP (Minimum Viable Product) and Phased Delivery: Prioritize use cases and requirements, define the MVP and pilot approach, and establish a phased implementation roadmap that balances customer value, feasibility, risk and reuse across platforms. Align Platform Initiatives: Coordinate with ongoing and planned portal initiatives across business platforms to ensure forward compatibility, common standards and a coherent One Lonza customer-facing experience. Embed Security, Quality and Compliance by Design: Ensure customer isolation, role-based access, auditability, data integrity, privacy, cybersecurity, IP protection and applicable GxP requirements are built into the portal design and delivery model. Establish Governance and Operating Model: Define portal ownership, decision rights, support processes, service levels, release and enhancement management, data stewardship and operational handover. Drive Cross-Functional Decision-Making: Align Commercial, Project Management, Operations, Quality, IT, Data, Enterprise Architecture, Security, Legal, Digital Marketing and platform stakeholders and resolve cross-functional dependencies and trade-offs. Manage Scope, Investment and Delivery: Maintain accountability for workstream scope, budget, schedule, resource plan, risks, dependencies, vendor contributions and delivery outcomes, escalating material deviations through the appropriate governance. Deliver Value and Adoption: Define success measures, validate customer and business value, prepare implementation recommendations, and drive adoption through stakeholder engagement, communication, training and continuous improvement. What we are looking for Bachelor or Master Business, Digital Product Management, Information Systems, Engineering, Life Sciences, Customer Experience or a related disciplineDigital Product Leadership: product vision, strategy, discovery, prioritization, roadmaps, MVP definition, release planning and lifecycle ownership.Requirements Definition & Translation: development of comprehensive user, business, functional and technical requirements for the portal, translate customer journeys and business processes into clear specifications and acceptance criteriaCustomer Experience Design: customer research, personas, journey mapping, service design, information architecture and experience measurement.Enterprise Platforms and Integration: understanding of identity and access management, APIs, workflow platforms, document and data exchange, integration patterns and enterprise architecture.Data and Governance Acumen: ability to translate governed data products, semantics, lineage, access controls and lifecycle requirements into customer-facing capabilities.Regulated Delivery: practical understanding of quality, GxP, data integrity, privacy, cybersecurity, IP and auditability considerations in digital product delivery.Commercial and Value Orientation: ability to connect portal capabilities to customer value, operational efficiency, differentiation, adoption and investment decisions.Stakeholder Alignment and Influence: ability to align executives, business owners, technical experts and external partners across organizational boundaries.Program and Vendor Management: strong governance, financial management, risk management, dependency management, sourcing and delivery oversight.English fluent 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.

Basel

Advanced Manufacturing Technology Lead

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s 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’s the kind of work we want to be part of.We are looking for Senior Director, Advanced Manufacturing Technology Lead to join our team!The Advanced Manufacturing Technology Lead defines and advances the cross-platform manufacturing technology agenda across Integrated Biologics, Advanced Synthesis and Specialized Modalities. The role identifies, evaluates and matures technologies that can materially improve productivity, autonomy, process control, quality assurance, flexibility and unit cost across manufacturing operations.The role focuses on reusable manufacturing technologies such as robotics, automation, automated material movement, smart sensing, PAT, process monitoring, process prediction, advanced control, digital twins and operator support technologies.The Advanced Manufacturing Technology Lead works closely with the Factory of the Future, Lab of the Future and Data Strategy & Products Leads to ensure technology solutions support the required manufacturing concepts, analytical capabilities and data needs, and can be scaled across platforms, sites and future builds. Key responsabilities:Technology Strategy & Roadmap• Define the cross-platform advanced manufacturing technology roadmap• Identify opportunities in robotics, automation, material movement, sensing, PAT, prediction and advanced process control• Assess technology maturity, applicability and scalability• Translate emerging technologies into prioritized manufacturing use casesLighthouse & Solution Development• Identify and prioritize cross-platform lighthouse opportunities• Drive technology assessment, partner selection and solution concept development• Ensure lighthouse solutions address clear operational or quality needs• Define success criteria and replication potentialIntegration with Manufacturing, Lab & Data• Translate manufacturing requirements into relevant technology solutions• Align sensing, monitoring and quality-related technologies with Lab of the Future• Align data and analytics requirements with Data Strategy & Products• Ensure solutions are integrated into coherent manufacturing conceptsScale-up & Replication• Convert proven solutions into reusable deployment requirements• Identify replication opportunities across platforms, sites and future builds• Support standardization of successful technologies and interfaces• Feed technology learnings into future manufacturing concepts and investment decisions Key requirements:• Bachelor or Master in Engineering, Automation, Robotics, Computer Science, or a related discipline• Highly Experienced in Advanced Manufacturing Technology, Automation & Operations Transformation• Highly Experienced in Development & Industrial Scale-Up• Ability to define cross-platform roadmaps across robotics, automation, material movement, sensing, PAT, prediction, advanced control, digital twins and operator-support technologies• Strong understanding of biopharmaceutical manufacturing, automation architectures, process monitoring and control, equipment interfaces and GMP requirements• Ability to quantify productivity, autonomy, quality, flexibility and unit-cost potential and translate it into prioritized use cases and investment cases• Ability to integrate equipment, automation, sensing, data, analytics and operator workflows into maintainable solutions with reusable interfaces• Demonstrated ability to lead multidisciplinary solution teams, assess suppliers and research partners, and drive concept development without relying on direct authority• Ability to communicate technology maturity, risks, architecture choices, evidence and recommendations clearly to technical, operational and executive stakeholders• Experience assessing readiness, technical and compliance risks, success criteria and dependencies and using evidence to support go, adapt or stop decisions• Ability to convert proven lighthouse solutions into reusable technical requirements, standards, interfaces and deployment recommendations across platforms, sites and future buildsEvery 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.

Basel