You will be based at our Visp site, supporting global warehouse and supply chain operations through SAP EWM solutions in a regulated GMP/ GxP environment. This role offers the opportunity to make a tangible impact on critical systems that enable reliable and compliant manufacturing.

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

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. Our full list of tailored local benefits can be found below.

Benefits in Visp: assetstream.aspx ()

What you will do:

Design, build, and enhance SAP EWM solutions supporting warehouse and labeling operations

Act as an IT business partner, translating business needs into functional specifications

Lead or contribute to initiatives as a functional lead

Configure and customize SAP EWM in line with global processes and governance

Support testing, validation, and audit readiness in a GMP/ GxP environment

Provide third level support for complex system incidents and problems

Drive continuous improvement by identifying optimization and innovation opportunities

What we are looking for:

Proven experience with SAP EWM and solid knowledge of SAP WM and SAP MM

Experience working with SAP S/4HANA EWM, embedded or decentralized

Experience working with complex automated warehouse environments; exposure to AGV-integrated landscapes, robotics, or warehouse control systems (WCS/MFS) is an advantage

Understanding of warehouse automation and system integration concepts

Previous experience in pharmaceutical or CDMO industries is preferred

Strong analytical skills with a structured approach to problem solving

Ability to collaborate and communicate effectively with stakeholders in English, German fluency is highly desired.

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.

Location: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.

For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.

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 dependant on role and location

The full list of our global benefits can be also found on .

What you will do:

Drive process standardization and efficiency in line with Lonza's LBMS standards

Support the implementation of a Lean Batch Release program on site

Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes

Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality

Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope

Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines

Share best practice within the Visp Site as well as with the wider Lonza Pharma network

What we are looking for:

University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)

Profound experience in a GMP regulated environment; preferably within QA/QC

Experience with Lean / Six Sigma, within a Quality related environment

Certified Green Belt or higher is required

PowerBI and/or Minitab knowledge would be an advantage

Fluent German (written and verbal) and good English language skills are required

Strong ability to collaborate effectively with colleagues across different functions

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.

Location: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.

For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.

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 dependant on role and location

The full list of our global benefits can be also found on .

What you will do:

Drive process standardization and efficiency in line with Lonza's LBMS standards

Support the implementation of a Lean Batch Release program on site

Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes

Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality

Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope

Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines

Share best practice within the Visp Site as well as with the wider Lonza Pharma network

What we are looking for:

University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)

Profound experience in a GMP regulated environment; preferably within QA/QC

Experience with Lean / Six Sigma, within a Quality related environment

Certified Green Belt or higher is required

PowerBI and/or Minitab knowledge would be an advantage

Fluent German (written and verbal) and good English language skills are required

Strong ability to collaborate effectively with colleagues across different functions

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.

Location: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.

For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.

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 dependant on role and location

The full list of our global benefits can be also found on .

What you will do:

Drive process standardization and efficiency in line with Lonza's LBMS standards

Support the implementation of a Lean Batch Release program on site

Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes

Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality

Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope

Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines

Share best practice within the Visp Site as well as with the wider Lonza Pharma network

What we are looking for:

University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)

Profound experience in a GMP regulated environment; preferably within QA/QC

Experience with Lean / Six Sigma, within a Quality related environment

Certified Green Belt or higher is required

PowerBI and/or Minitab knowledge would be an advantage

Fluent German (written and verbal) and good English language skills are required

Strong ability to collaborate effectively with colleagues across different functions

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.

Location: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.

For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.

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 dependant on role and location

The full list of our global benefits can be also found on .

What you will do:

Drive process standardization and efficiency in line with Lonza's LBMS standards

Support the implementation of a Lean Batch Release program on site

Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes

Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality

Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope

Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines

Share best practice within the Visp Site as well as with the wider Lonza Pharma network

What we are looking for:

University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)

Profound experience in a GMP regulated environment; preferably within QA/QC

Experience with Lean / Six Sigma, within a Quality related environment

Certified Green Belt or higher is required

PowerBI and/or Minitab knowledge would be an advantage

Fluent German (written and verbal) and good English language skills are required

Strong ability to collaborate effectively with colleagues across different functions

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.

Location: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.

For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.

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 dependant on role and location

The full list of our global benefits can be also found on .

What you will do:

Drive process standardization and efficiency in line with Lonza's LBMS standards

Support the implementation of a Lean Batch Release program on site

Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes

Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality

Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope

Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines

Share best practice within the Visp Site as well as with the wider Lonza Pharma network

What we are looking for:

University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)

Profound experience in a GMP regulated environment; preferably within QA/QC

Experience with Lean / Six Sigma, within a Quality related environment

Certified Green Belt or higher is required

PowerBI and/or Minitab knowledge would be an advantage

Fluent German (written and verbal) and good English language skills are required

Strong ability to collaborate effectively with colleagues across different functions

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.

Associate Director, Technical Sales

Location: Visp with Relocation and Visa support is to be offered

Today, Lonza is a global leader in life sciences operating across five continents.

As an Associate Director, Technical Sales, you will help guide customers toward the best technical and commercial solutions across Lonza's platforms. In this role, you will use your scientific expertise and strategic mindset to shape high value opportunities, collaborate with global teams, and contribute directly to the growth of our business.

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

The full list of our global benefits can be found here:

What you will do

Lead integrated offer development for Advanced Synthesis and represent the platform in global strategic initiatives.

Manage a global team of technical sales professionals and support their growth and performance.

Improve processes, tools, and templates used to create integrated offers for ADCs and XDCs.

Contribute to preparing contract templates, including terms, conditions, and master service agreements.

Ensure accurate costing and proposal inputs using approved tools and methods.

Collaborate with cross functional teams to build executable, customer focused proposals.

Support customer engagements by preparing proposals, leading discussions, and participating in evaluations.

What we are looking for

Preferably PHD or a MSc in a scientific field or equivalent relevant experience.

Fluency in English; German language skills are an advantage.

10+ years of experience in the pharmaceutical or biotech industry.

Proven experience leading and developing teams.

Strong understanding of integrated services and manufacturing processes.

Excellent communication, analytical thinking, and collaborative skills.

Knowledge of CDMO operations and Lonza's cross platform offerings.

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.

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:

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 Ingenieur in (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!