Lonza jobs

Relocation assistance is available for eligible candidates and their families, ensuring a smooth transition to our welcoming community in Visp. Today, Lonza is a global leader in life sciences operating across three 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. For our site in Visp, we are currently seeking several qualified Pipe Fitters / Metalworkers. What you’ll get: - An agile career and dynamic working culture - An inclusive and ethical workplace - Compensation programs that recognize high performance - Along with competitive salaries, you’ll find a wide range of lifestyle, family and leisure benefits available. Your Responsibilities: - Professionally and cost-effectively measure, fabricate, and install complex piping systems and support structures in industrial piping construction - Prepare isometric drawings and piping spool assemblies in accordance with technical specifications and project requirements - Plan and organize work processes based on P&ID flow diagrams for project work and plant modifications - Apply PED directives and work according to internal piping classes, plant standards, and quality assurance requirements Your Profile: - Completed vocational training as a technician specializing in piping construction, pipefitting, heating installation, or plumbing installation. - Several years of professional experience as a pipefitter or piping preparator/fabricator is an advantage - Willingness to pursue continuous professional development - Enjoy working across departments and capable of working independently and flexibly within a team - Reliable, resilient, entrepreneurial mindset, with open and direct communication skills - Good command of German, both written and spoken; English skills are an advantage 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.

Sofern erforderlich, steht berechtigten Kandidaten und ihren Familien Unterstützung beim Umzug zur Verfügung. Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen. Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen. Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig. Denn ihre Ideen, ob gross und klein, verbessern die Welt. Und das ist die Art von Arbeit, an der wir Teil haben möchten. Zur Verstärkung des Teams am Standort Visp wird eine erfahrene Persönlichkeit für die fachliche Leitung eines EMR-Subteams gesucht. Im Fokus stehen Projektierung, Instandhaltung, Dokumentation, Know-how-Transfer sowie die Einhaltung von GMP- und Sicherheitsvorschriften. Was wir dir bieten: - Eine agile Karriere und eine dynamische Arbeitskultur - Einen integrativen und ethischen Arbeitsplatz - Vergütungsprogramme, die hohe Leistung anerkennen - Neben einem wettbewerbsfähigen Gehalt erwarten dich zahlreiche Vorteile in den Bereichen Lifestyle, Familie und Freizeit. Die vollständige Liste unserer globalen Leistungen findest du auch unter: https://bit.ly/3wjkoFi Deine Aufgaben: - Planung und Umsetzung von Automatisierungsprojekten (Anlagenoptimierungen, Erweiterungen, Produkteumstellungen) - Technische Verantwortung über alle Projektphasen – von der Konzeption bis zur Inbetriebnahme - Mitarbeit in interdisziplinären Projektteams sowie Teilnahme an Risikoanalysen und Betriebsversuchen - Sicherstellung einer zuverlässigen, wirtschaftlichen Instandhaltung im GMP-regulierten Umfeld - Koordination von internen und externen Partnern sowie Überwachung des Instandhaltungsbudgets - Pflege und laufende Aktualisierung der Anlagendokumentation (SAP, COMOS) - Verantwortung für GMP-gerechtes Änderungsmanagement und Systempflege - Fachliche Betreuung definierter EMR-Bereiche sowie Weitergabe von Know-how an Werkstatt- und Betriebspersonal - Einhaltung und Umsetzung geltender GMP-, Sicherheits- und Umweltvorgaben Dein Profil: - Abgeschlossenes Studium als Ingenieurin (ETH, FH, HF) in Elektro-, Automations- oder Systemtechnik - Mehrjährige Erfahrung im Betrieb, in der Instandhaltung oder im Anlagenbau in einem GMP-regulierten Umfeld - Kenntnisse in SAP, COMOS, DeltaV, MES von Vorteil - Sehr gute Deutschkenntnisse in Wort und Schrift, gute Englischkenntnisse - Strukturierte und selbständige Arbeitsweise mit hoher Eigenverantwortung - Teamorientiertes Denken, klare Kommunikation und hohe Belastbarkeit - Offen für neue Technologien und agile Arbeitsweisen Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus. Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar. Wie wir unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst. Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt. Erfolg für uns bedeutet moralisch vertretbarer Fortschritt. Menschen werden Teil der Lonza, um herausfordernde und komplexe Problemstellungen durch kreative und innovative Ansätze im Bereich Life Sciences zu lösen. Im Gegenzug bieten wir die Zufriedenheit, die mit der Verbesserung des Lebens auf der ganzen Welt einhergeht. Die Zufriedenheit, die damit einhergeht, einen sinnvollen Unterschied zu machen. Bereit, die Zukunft der Life Sciences mitzugestalten? Dann bewirb dich jetzt!

The actual location of this job is in Stein, AG, Switzerland . Relocation assistance is available for eligible candidates and their families, if needed. Lead a high-impact MSAT team through a demanding CAPEX growth project ramp-up—driving Performance Qualifications (PPQs), aseptic process simulations (media fills), and equipment/process qualifications (PQs) for sterile fill & finish lines, supporting technology transfers, and ensuring successful operational readiness. Build accountability, manage performance, deliver under pressure, and shape a resilient, future-ready culture. We are seeking an authentic leader with proven people leadership experience (including performance management and difficult conversations), strong resilience, and deep expertise in MSAT and sterile fill-finish manufacturing. Experience with lyophilization and/or ADCs is a strong advantage. You will lead the team through facility ramp-up, PPQ execution, aseptic process simulations, technology transfers, inspection readiness, and operational challenges while inspiring a diverse organization through growth and change. Check out Your Career in Drug Product Services at Lonza ! 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 will get: - An agile career and a dynamic work culture. - An inclusive and ethical workplace. - Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits What you will do: - Lead and develop a high-performing MSAT organization responsible for facility ramp-up, process implementation, technology transfers, aseptic process simulations (media fills), process performance qualifications (PPQs), and lifecycle process support. Provide full people leadership responsibility, including talent development, performance management, succession planning, and organizational design. Foster a culture of accountability, empowerment, innovation, resilience, and continuous improvement while ensuring effective utilization of personnel, equipment, materials, and facility resources. - Own the technical implementation and qualification strategy for manufacturing processes within the facility, ensuring compliance with Lonza standards, customer requirements, GMP regulations, and industry best practices. Drive successful execution of process qualifications, validation activities, and operational readiness milestones to support commercial manufacturing. - Ensure inspection readiness at all times and serve as a key representative during regulatory inspections, customer audits, and due diligence visits. Present technical strategies, validation approaches, process performance, and investigation outcomes to customers and health authorities with confidence and credibility. - Partner with Operation and Engineering teams to define and deliver strategic priorities, operational objectives, and long-term capability development plans aligned with site, business unit, and corporate goals. Contribute actively to the overall leadership and performance of the site. - Collaborate across functions and sites including Operations, Quality, Engineering, Validation, Process Development, Analytical Development, Regulatory Affairs, and Global MSAT to ensure seamless technology transfers, robust process control strategies, and successful commercialization of new products. Act as deputy to the Head of Drug Product Operations Stein as required. - Establish and continuously improve MSAT standards, systems, and processes , including qualification and validation strategies, single-use technologies, process monitoring, continued process verification, and lifecycle management. Ensure application of scientific and risk-based approaches to process design, qualification, and optimization. - Lead complex product and process investigations , deviations, CAPAs, complaints, and troubleshooting activities. Apply strong scientific, engineering, and statistical expertise to analyze data, identify root causes, assess process capability, and implement sustainable corrective and preventive actions. - Serve as technical authority for manufacturing science and technology , providing expert support and coaching to scientific, technical, and production teams. Drive knowledge sharing, innovation, and continuous improvement to enhance process robustness, operational excellence, and product quality. What we are looking for: - Proven team leadership experience , including conducting performance discussions and managing performance effectively (experience from MSAT, QA, or Manufacturing environments) - Strong resilience , with the ability to stay composed and lead under pressure in a demanding and evolving environment - Demonstrated expertise in sterile fill & finish manufacturing (essential) - Ability to lead with authenticity and positivity , providing clear direction, perspective, and fostering accountability within the team - Solid background in MSAT operations , with experience in technology transfer and process implementation (highly preferred) - Scientific degree (natural sciences) preferred; additional expertise in lyophilization and/or ADC (antibody-drug conjugates) is a strong advantage 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.

The actual location of this job is in Stein, AG, Switzerland . Relocation assistance is available for eligible candidates and their families, if needed. Lead a high-impact MSAT team through a demanding CAPEX growth project ramp-up—driving Performance Qualifications (PPQs), aseptic process simulations (media fills), and equipment/process qualifications (PQs) for sterile fill & finish lines, supporting technology transfers, and ensuring successful operational readiness. Build accountability, manage performance, deliver under pressure, and shape a resilient, future-ready culture. We are seeking an authentic leader with proven people leadership experience (including performance management and difficult conversations), strong resilience, and deep expertise in MSAT and sterile fill-finish manufacturing. Experience with lyophilization and/or ADCs is a strong advantage. You will lead the team through facility ramp-up, PPQ execution, aseptic process simulations, technology transfers, inspection readiness, and operational challenges while inspiring a diverse organization through growth and change. Check out Your Career in Drug Product Services at Lonza ! 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 will get: - An agile career and a dynamic work culture. - An inclusive and ethical workplace. - Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits What you will do: - Lead and develop a high-performing MSAT organization responsible for facility ramp-up, process implementation, technology transfers, aseptic process simulations (media fills), process performance qualifications (PPQs), and lifecycle process support. Provide full people leadership responsibility, including talent development, performance management, succession planning, and organizational design. Foster a culture of accountability, empowerment, innovation, resilience, and continuous improvement while ensuring effective utilization of personnel, equipment, materials, and facility resources. - Own the technical implementation and qualification strategy for manufacturing processes within the facility, ensuring compliance with Lonza standards, customer requirements, GMP regulations, and industry best practices. Drive successful execution of process qualifications, validation activities, and operational readiness milestones to support commercial manufacturing. - Ensure inspection readiness at all times and serve as a key representative during regulatory inspections, customer audits, and due diligence visits. Present technical strategies, validation approaches, process performance, and investigation outcomes to customers and health authorities with confidence and credibility. - Partner with Operation and Engineering teams to define and deliver strategic priorities, operational objectives, and long-term capability development plans aligned with site, business unit, and corporate goals. Contribute actively to the overall leadership and performance of the site. - Collaborate across functions and sites including Operations, Quality, Engineering, Validation, Process Development, Analytical Development, Regulatory Affairs, and Global MSAT to ensure seamless technology transfers, robust process control strategies, and successful commercialization of new products. Act as deputy to the Head of Drug Product Operations Stein as required. - Establish and continuously improve MSAT standards, systems, and processes , including qualification and validation strategies, single-use technologies, process monitoring, continued process verification, and lifecycle management. Ensure application of scientific and risk-based approaches to process design, qualification, and optimization. - Lead complex product and process investigations , deviations, CAPAs, complaints, and troubleshooting activities. Apply strong scientific, engineering, and statistical expertise to analyze data, identify root causes, assess process capability, and implement sustainable corrective and preventive actions. - Serve as technical authority for manufacturing science and technology , providing expert support and coaching to scientific, technical, and production teams. Drive knowledge sharing, innovation, and continuous improvement to enhance process robustness, operational excellence, and product quality. What we are looking for: - Proven team leadership experience , including conducting performance discussions and managing performance effectively (experience from MSAT, QA, or Manufacturing environments) - Strong resilience , with the ability to stay composed and lead under pressure in a demanding and evolving environment - Demonstrated expertise in sterile fill & finish manufacturing (essential) - Ability to lead with authenticity and positivity , providing clear direction, perspective, and fostering accountability within the team - Solid background in MSAT operations , with experience in technology transfer and process implementation (highly preferred) - Scientific degree (natural sciences) preferred; additional expertise in lyophilization and/or ADC (antibody-drug conjugates) is a strong advantage 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.

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. We are looking to recruit a Manufacturing Lead (Director) to build up the operations organization for the Payload-Linker capacity expansion in Visp . Leads a team of  production leaders, supervisors and specialists You will manage the operational readiness and provide leadership to the CQ-project team incl. the post OQ Start-up within the investment / Capex Project. After becoming operational , you will oversee the operational activities of the manufacturing unit with overall responsibility of manufacturing execution regarding safety, quality and on-time-in full delivery, as well as for the performance and results of the assigned area including cost control. What you’ll 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. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits . What you will do: - Lead a team of production managers (chemists/chemical engineers), supervisors, and specialists, with full responsibility for all aspects of people management, including qualification, development, coaching, hiring, compensation decisions, and performance or conduct issues. - Manage the operational readiness within the CAPEX project and provide leadership to the CQ-project team incl. the post OQ Start-up - Accountable for executing all production campaigns in the manufacturing unit, ensuring compliance with safety, quality, and environmental requirements. - Maintain oversight of production costs and provide POV forecasts for all campaigns within the area of responsibility. Contribute to budgeting and the preparation of product cost calculations for standard pricing. - As a member of the Functional Leadership Team, support overall production management, including housekeeping, team conduct, training activities, and general operational controls. - Serve as an operational specialist and regular point of contact for BU team members on production planning (S&OP), technical assessments, and feasibility requests. - Responsible for routine performance monitoring, including weekly reports, dashboards, Hoshin boards, and other reporting tools. What we are looking for: - Advanced degree (Master’s, PhD, or equivalent) in Chemistry, Chemical Engineering, or a related field. - Demonstrated leadership skills with strong self-motivation, integrity, perseverance, and results orientation. - Extensive experience in chemical manufacturing in the pharmaceutical industry, in leadership roles. - Strong knowledge of GMP and EHS requirements. - Fluency in English, German is an advantage - Experience with Operational Excellence / LEAN principles is an advantage. 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.

Sofern erforderlich, steht berechtigten Kandidaten und ihren Familien Unterstützung beim Umzug zur Verfügung. Werde Teil unseres Werkstatt-Teams als Automatiker ! In dieser vielseitigen Funktion übernimmst du die Verantwortung für sämtliche Automatisierungsaufgaben im Rahmen der reaktiven, proaktiven und präventiven Instandhaltung. Mit deinem Fachwissen sorgst du für einen zuverlässigen und effizienten Anlagenbetrieb und leistest einen wesentlichen Beitrag zur hohen Anlagenverfügbarkeit, Produktqualität sowie zur Einhaltung aller Compliance-Anforderungen an unserem Standort in Visp. Was wir dir bieten: - Eine agile Karriere und eine dynamische Arbeitskultur - Einen integrativen und ethischen Arbeitsplatz - Vergütungsprogramme, die hohe Leistung anerkennen - Neben einem wettbewerbsfähigen Gehalt erwarten dich zahlreiche Vorteile in den Bereichen Lifestyle, Familie und Freizeit. Die vollständige Liste unserer globalen Leistungen findest du auch unter: assetstream.aspx Deine Aufgaben: - Durchführung von Inbetriebsetzungsarbeiten und Störungsbehebung von EMR-Anlagen (Elektro-, Mess- und Regeltechnik) - Präventive Instandhaltung von EMR-Anlagen - Kalibrierung, Kontrolle und Handhabung von Messmitteln - Dokumentation nach GxP Richtlinien (Datenintegrität) - Übernahme von Pikettdienst bei Bedarf Dein Profil: - Abgeschlossene Ausbildung zum Automatiker EFZ, Elektroinstallateur EFZ, Elektroniker EFZ oder einem artverwandten Beruf - Grundkenntnisse Mess- und Regeltechnik sind von Vorteil - Bereitschaft zu kontinuierlicher Weiterbildung - Freude an abteilungsübergreifender Arbeit sowie selbstständiges und flexibles Arbeiten im Team - Zuverlässigkeit, Belastbarkeit sowie unternehmerisches Handeln und offene, direkte Kommunikation - Deutschkenntnisse in Wort und Schrift, Englischkenntnisse von Vorteil 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 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!

The actual location of this job is in Stein, AG, Switzerland . Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza as an Associate Director, Technology Transfer (Global MSAT) and play a pivotal role in bringing complex drug products from development to commercial reality. You’ll lead end-to-end technology transfers —from process scale-up and PPQ to regulatory filings, inspection readiness, and successful launch with a focus on aseptic fill&finish processes. Check out Your Career in Drug Product Services at Lonza ! 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 will get: - An agile career and a dynamic work culture. - An inclusive and ethical workplace. - Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits What you will do: - Manage, drive and guide high‑complexity and high-impact drug product commercial transfers from New Product Introduction to PPQ, regulatory filing, pre-approval health authority inspections and first commercial launch. - Act as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy, ensuring global standard alignment, and driving customer‑centric excellence across sites and product lifecycles. - Provide technical authority and act as senior escalation point for complex technical challenges, provide tech transfer leadership for late‑phase and commercial programs. - Serve as the primary technical point of contact for all technology‑transfer‑related manufacturing topic of assigned projects within internal and customer project teams. Define and monitor project scope, timing and progress of assigned stages. - Lead process setup, scale‑up, and implementation activities at GMP drug product manufacturing sites, including on‑site technical support during batch execution. - Responsible for new product introduction, process implementation, process control strategy and technical transfer and process validation documentation of assigned projects, including review of dossier modules for regulatory filing. - Drive GMP change management strategy of assigned projects as well as initiate and manage GMP change control in system. Lead and support critical GMP product / process deviations and corresponding implementation of corrective/preventive actions (CAPAs). - Ensure all activities are performed according to current standards (Good Manufacturing Practice, Health Safety Environment, Regulatory etc.). What we are looking for: - Industry-leading expertise in biotech/pharma/CDMO environments , with strong experience in drug product development, tech transfer especially within aseptic fill&finish processes (e.g. lyophilization, prefilled syringes). Proven ability to translate scientific depth into strategic decision‑making. - Deep knowledge of GMP, regulatory, and CMC requirements , with the ability to translate strategy into robust manufacturing execution - Proven ability to influence and lead complex manufacturing strategies and resolve high-impact technical challenges across global, cross-site operations - Strong communication and stakeholder engagement skills , influencing senior leaders and navigating complex decision-making environments - University degree in Biochemistry, Pharmaceutical Science or similar field (PhD preferred) - Excellent project, risk, and data management capabilities , paired with clear technical writing; fluent in English (German is a plus) 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.

Internal Auditor/Internal Audit Manager (with experience in Operations and/or Project Management) Location – Basel, Switzerland. Relocation assistance is available for eligible candidates and their families if needed For our small, but impactful internal audit team, we are looking for a highly motivated and talented auditor or audit manager. Your task will be to support or lead/execute internal audit assignments within the Lonza Group, while getting to know the business and developing your expertise for a line management career. Lonza Audit Services (LAS) provides the board and management with independent, risk-based and objective assurance, advice, insight, and foresight. The function is independently positioned with direct accountability to the Board; it works with the management and reviews activities in the organization, reports observations, risks and recommendations to the audited parties, senior management, Executive Committee as well as to the Audit & Compliance Committee. 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 - A variety of benefits tailored to your localality. - Access to global benefits via https://www.lonza.com/careers/benefits What you will do: - As an auditor, prepare, execute and conduct assigned internal audit activities; as a manager, plan lead and deliver internal audit assignments, including coverage of occasional consulting / advisory engagements in any operational area or covering special projects and strategic initiatives of the company - As an auditor, support and cooperate with the audit team; as a team lead, train, supervise and guide team member(s) and/or outsourced experts assigned to individual engagements - Present audit results to stakeholders; prepare clear and concise audit reports that effectively communicate key findings, root causes, and associated risks. - Cooperate with internal experts to optimize audit preparations and execution with data analytics and SAP configuration reviews; support corresponding activities related to ongoing improvements of audit programs and processes - Participate in discussions with parts of the organization and global process owners, especially regarding best practices as well as standardization and harmonization of processes and controls - Follow-up on audit recommendations’ implementation and support the reporting on open and overdue issues to top management - Lead initiatives and/or contribute to other internal activities and projects constantly optimizing the Internal Audit function What we are looking for: - Master degree preferably in finance / accounting, degree in chemistry or similar also welcome - 3+ years of internal audit experience, complemented by hands-on experience in operations or project delivery (e.g., project management experience, with a solid understanding of project lifecycles, governance, and execution risks) - Very experienced in executing assignments in compliance with international auditing standards; excellent understanding of standard business processes like S2P, OTC, R2R with solid know-how of SAP - Excellent command of written and spoken English - Passionate about leveraging AI and digital tools; knowledge of ETL concepts and familiarity with SQL, Python programming and/or Power BI dashboards a plus - Good analytical skills, risk focused, target and deadline oriented, result driven and solution developer, motivated self-starter - Team player and very good communicator with leadership skills and potential to develop career further within the Lonza Group after 3-4 years in internal auditing - Excellent command of written and spoken English - Travel requirements approximately 10-20% 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.

Umzugsunterstützung steht berechtigen Kandidaten und ihren Familien bei Bedarf zur Verfügung. Werde Teil unseres Werkstatt-Teams als Anlagen- und Apparatebauer! In dieser abwechslungsreichen Funktion übernimmst du anspruchsvolle Arbeiten im Bereich Rohrbau sowie die reaktive, proaktive und präventive Instandhaltung unserer Produktionsanlagen. Mit deinem handwerklichen Geschick und deinem technischen Fachwissen stellst du die sichere und zuverlässige Funktion unserer Rohrleitungssysteme sicher. So leistest du einen wichtigen Beitrag zur hohen Anlagenverfügbarkeit, Produktqualität sowie zur Einhaltung unserer Qualitäts-, Sicherheits- und Compliance-Standards am Standort Visp. Was wir dir bieten: - Eine agile Karriere und eine dynamische Arbeitskultur - Einen integrativen und ethischen Arbeitsplatz - Vergütungsprogramme, die hohe Leistung anerkennen - Neben einem wettbewerbsfähigen Gehalt erwarten dich zahlreiche Vorteile in den Bereichen Lifestyle, Familie und Freizeit. Die vollständige Liste unserer globalen Leistungen findest du auch unter: https://bit.ly/3wjkoFi Deine Aufgaben: - Fachgerechtes und wirtschaftliches Ausmessen, Herstellen und Montieren von anspruchsvollen Rohrleitungen und Stützsystemen im Rohrleitungsbau - Erstellen von Isometrien und Rohrleitungssegmenten entsprechend den technischen Vorgaben und Projektanforderungen - Planen und Organisieren der Arbeitsabläufe anhand von R&I‑Fliessbildern, bei Projektarbeiten und Anlagenanpassungen - Anwenden von PED‑Richtlinien sowie Arbeiten nach internen Rohrklassen, Werknormen und qualitätssichernden Vorgaben Dein Profil: - Abgeschlossene Ausbildung zum Anlagen- und Apparatebauer EFZ in Rohrleitungsbau, Rohrschlosser, Heizungsmonteur oder Sanitär-Installateur - Mehrjährige Berufserfahrung als Rohrschlosser oder Vorrichter von Vorteil - Bereitschaft zu kontinuierlicher Weiterbildung - Freude an abteilungsübergreifender Arbeit sowie selbstständiges und flexibles Arbeiten im Team - Zuverlässigkeit, Belastbarkeit sowie unternehmerisches Handeln und offene, direkte Kommunikation - Deutschkenntnisse in Wort und Schrift, Englischkenntnisse von Vorteil 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 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!