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.

We are looking for a DeltaV Automation Engineer or Electrical Instrumentation & Control Engineer (m/f/d) to join us in a dynamic, cutting-edge environment where your work will significantly contribute to shaping the future of medicine.

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 dependant on role and location

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

What you will do:

Planning and realization of electrical MSR readiness (maintenance, changeovers, improvements) within the available budget and timelines

Ensuring seamless operation and flawless performance of high-automated Biologics facilities equipped with DeltaV and MES systems. Equivalent experience is also acceptable for educational requirements like MES

Managing GMP-compliant activities, including testing, documentation, and change management using systems such as Kneat and Ubik

Preparing and updating plant documentation in SAP/COMOS to ensure strict compliance with regulatory standards

Determining and implementing continuous improvements in equipment and maintenance processes to improve efficiency and reliability

Collaborating with cross-functional teams to refine internal procedures and achieve optimized workflows

What we are looking for:

Equivalent experience in Electrical or System Engineering or a related field, including University Degree or equivalent experience, or vocational education (EFZ, FH, HF, BSc.)

Proven experience in the operation and maintenance of pharmaceutical plants or the biotech industry

Proficiency in SAP, COMOS (Plant Engineering Software), DeltaV (Process Control System), and MES Syncade (Manufacturing Execution System) is highly desirable

Proficient in English and/or German to competently communicate in our diverse, collaborative environment

Familiarity with GMP standards and protocols to ensure compliance in a regulated manufacturing setting

A self-reliant, trustworthy, and effective working approach that ensures successful completion of tasks and projects

Relocation assistance is available for eligible candidates and their families, ensuring a smooth transition to our welcoming community in Visp.

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.

Location. 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.

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 dependant on role and location.

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

What you'll do :

Carry out end to end Drug Product manufacturing under GMP: batch execution, documentation, troubleshooting, and review of results.

Complete and maintain all GMP documentation (batch records, logbooks, forms). Support process changes and CAPA activities.

Ensure every batch is made safely, on time, and according to quality and aseptic standards.

Set up, operate, and clean equipment for liquid and freeze dried (lyophilized) vial manufacturing.

Support compounding & formulations, buffer preparation, washing/autoclaving, filter integrity testing, filling/crimping, and visual inspection.

Experience with aseptic handling inside isolators or conventional cleanrooms, or work with single use components is a major plus.

Train colleagues and support cross functional teams with technical guidance.

Report equipment issues and support engineering teams with repairs in cleanroom/aseptic areas.

What we're looking for :

2-4 years of GMP shopfloor experience (ideally sterile Drug Product / Fill & Finish).

Drug Product experience is a strong advantage. EFZ apprenticeship (mechanic or similar: production mechanic, car mechanic, etc.) Also practical experience in professions with high hygiene and cleanliness requirements, such as cook/chef or comparable roles.

Good English skills for instructions and communication; German is a plus.

Familiarity with GMP, SOPs, and quality processes.

Reliable, well organized, team oriented working style.

IT knowledge (SAP/MES is a plus).

Willingness to support on call duties to some extent.

Currently operating in a 2 shift system; readiness for 3 shift work (regular 5 day week, occasional Saturday, no Sundays).

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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.

We are looking for a DeltaV Automation Engineer or Electrical Instrumentation & Control Engineer (m/f/d) to join us in a dynamic, cutting-edge environment where your work will significantly contribute to shaping the future of medicine.

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 dependant on role and location

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

What you will do:

Planning and realization of electrical MSR readiness (maintenance, changeovers, improvements) within the available budget and timelines

Ensuring seamless operation and flawless performance of high-automated Biologics facilities equipped with DeltaV and MES systems. Equivalent experience is also acceptable for educational requirements like MES

Managing GMP-compliant activities, including testing, documentation, and change management using systems such as Kneat and Ubik

Preparing and updating plant documentation in SAP/COMOS to ensure strict compliance with regulatory standards

Determining and implementing continuous improvements in equipment and maintenance processes to improve efficiency and reliability

Collaborating with cross-functional teams to refine internal procedures and achieve optimized workflows

What we are looking for:

Equivalent experience in Electrical or System Engineering or a related field, including University Degree or equivalent experience, or vocational education (EFZ, FH, HF, BSc.)

Proven experience in the operation and maintenance of pharmaceutical plants or the biotech industry

Proficiency in SAP, COMOS (Plant Engineering Software), DeltaV (Process Control System), and MES Syncade (Manufacturing Execution System) is highly desirable

Proficient in English and/or German to competently communicate in our diverse, collaborative environment

Familiarity with GMP standards and protocols to ensure compliance in a regulated manufacturing setting

A self-reliant, trustworthy, and effective working approach that ensures successful completion of tasks and projects

Relocation assistance is available for eligible candidates and their families, ensuring a smooth transition to our welcoming community in Visp.

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.

Location. 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.

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 dependant on role and location.

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

What you'll do :

Carry out end to end Drug Product manufacturing under GMP: batch execution, documentation, troubleshooting, and review of results.

Complete and maintain all GMP documentation (batch records, logbooks, forms). Support process changes and CAPA activities.

Ensure every batch is made safely, on time, and according to quality and aseptic standards.

Set up, operate, and clean equipment for liquid and freeze dried (lyophilized) vial manufacturing.

Support compounding & formulations, buffer preparation, washing/autoclaving, filter integrity testing, filling/crimping, and visual inspection.

Experience with aseptic handling inside isolators or conventional cleanrooms, or work with single use components is a major plus.

Train colleagues and support cross functional teams with technical guidance.

Report equipment issues and support engineering teams with repairs in cleanroom/aseptic areas.

What we're looking for :

2-4 years of GMP shopfloor experience (ideally sterile Drug Product / Fill & Finish).

Drug Product experience is a strong advantage. EFZ apprenticeship (mechanic or similar: production mechanic, car mechanic, etc.) Also practical experience in professions with high hygiene and cleanliness requirements, such as cook/chef or comparable roles.

Good English skills for instructions and communication; German is a plus.

Familiarity with GMP, SOPs, and quality processes.

Reliable, well organized, team oriented working style.

IT knowledge (SAP/MES is a plus).

Willingness to support on call duties to some extent.

Currently operating in a 2 shift system; readiness for 3 shift work (regular 5 day week, occasional Saturday, no Sundays).

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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.

We are looking for a DeltaV Automation Engineer or Electrical Instrumentation & Control Engineer (m/f/d) to join us in a dynamic, cutting-edge environment where your work will significantly contribute to shaping the future of medicine.

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 dependant on role and location

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

What you will do:

Planning and realization of electrical MSR readiness (maintenance, changeovers, improvements) within the available budget and timelines

Ensuring seamless operation and flawless performance of high-automated Biologics facilities equipped with DeltaV and MES systems. Equivalent experience is also acceptable for educational requirements like MES

Managing GMP-compliant activities, including testing, documentation, and change management using systems such as Kneat and Ubik

Preparing and updating plant documentation in SAP/COMOS to ensure strict compliance with regulatory standards

Determining and implementing continuous improvements in equipment and maintenance processes to improve efficiency and reliability

Collaborating with cross-functional teams to refine internal procedures and achieve optimized workflows

What we are looking for:

Equivalent experience in Electrical or System Engineering or a related field, including University Degree or equivalent experience, or vocational education (EFZ, FH, HF, BSc.)

Proven experience in the operation and maintenance of pharmaceutical plants or the biotech industry

Proficiency in SAP, COMOS (Plant Engineering Software), DeltaV (Process Control System), and MES Syncade (Manufacturing Execution System) is highly desirable

Proficient in English and/or German to competently communicate in our diverse, collaborative environment

Familiarity with GMP standards and protocols to ensure compliance in a regulated manufacturing setting

A self-reliant, trustworthy, and effective working approach that ensures successful completion of tasks and projects

Relocation assistance is available for eligible candidates and their families, ensuring a smooth transition to our welcoming community in Visp.

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.

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.

We are looking for a DeltaV Automation Engineer or Electrical Instrumentation & Control Engineer (m/f/d) to join us in a dynamic, cutting-edge environment where your work will significantly contribute to shaping the future of medicine.

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 dependant on role and location

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

What you will do:

Planning and realization of electrical MSR readiness (maintenance, changeovers, improvements) within the available budget and timelines

Ensuring seamless operation and flawless performance of high-automated Biologics facilities equipped with DeltaV and MES systems. Equivalent experience is also acceptable for educational requirements like MES

Managing GMP-compliant activities, including testing, documentation, and change management using systems such as Kneat and Ubik

Preparing and updating plant documentation in SAP/COMOS to ensure strict compliance with regulatory standards

Determining and implementing continuous improvements in equipment and maintenance processes to improve efficiency and reliability

Collaborating with cross-functional teams to refine internal procedures and achieve optimized workflows

What we are looking for:

Equivalent experience in Electrical or System Engineering or a related field, including University Degree or equivalent experience, or vocational education (EFZ, FH, HF, BSc.)

Proven experience in the operation and maintenance of pharmaceutical plants or the biotech industry

Proficiency in SAP, COMOS (Plant Engineering Software), DeltaV (Process Control System), and MES Syncade (Manufacturing Execution System) is highly desirable

Proficient in English and/or German to competently communicate in our diverse, collaborative environment

Familiarity with GMP standards and protocols to ensure compliance in a regulated manufacturing setting

A self-reliant, trustworthy, and effective working approach that ensures successful completion of tasks and projects

Relocation assistance is available for eligible candidates and their families, ensuring a smooth transition to our welcoming community in Visp.

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.

Location. 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.

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 dependant on role and location.

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

What you'll do :

Carry out end to end Drug Product manufacturing under GMP: batch execution, documentation, troubleshooting, and review of results.

Complete and maintain all GMP documentation (batch records, logbooks, forms). Support process changes and CAPA activities.

Ensure every batch is made safely, on time, and according to quality and aseptic standards.

Set up, operate, and clean equipment for liquid and freeze dried (lyophilized) vial manufacturing.

Support compounding & formulations, buffer preparation, washing/autoclaving, filter integrity testing, filling/crimping, and visual inspection.

Experience with aseptic handling inside isolators or conventional cleanrooms, or work with single use components is a major plus.

Train colleagues and support cross functional teams with technical guidance.

Report equipment issues and support engineering teams with repairs in cleanroom/aseptic areas.

What we're looking for :

2-4 years of GMP shopfloor experience (ideally sterile Drug Product / Fill & Finish).

Drug Product experience is a strong advantage. EFZ apprenticeship (mechanic or similar: production mechanic, car mechanic, etc.) Also practical experience in professions with high hygiene and cleanliness requirements, such as cook/chef or comparable roles.

Good English skills for instructions and communication; German is a plus.

Familiarity with GMP, SOPs, and quality processes.

Reliable, well organized, team oriented working style.

IT knowledge (SAP/MES is a plus).

Willingness to support on call duties to some extent.

Currently operating in a 2 shift system; readiness for 3 shift work (regular 5 day week, occasional Saturday, no Sundays).

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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.

We are looking for a DeltaV Automation Engineer or Electrical Instrumentation & Control Engineer (m/f/d) to join us in a dynamic, cutting-edge environment where your work will significantly contribute to shaping the future of medicine.

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 dependant on role and location

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

What you will do:

Planning and realization of electrical MSR readiness (maintenance, changeovers, improvements) within the available budget and timelines

Ensuring seamless operation and flawless performance of high-automated Biologics facilities equipped with DeltaV and MES systems. Equivalent experience is also acceptable for educational requirements like MES

Managing GMP-compliant activities, including testing, documentation, and change management using systems such as Kneat and Ubik

Preparing and updating plant documentation in SAP/COMOS to ensure strict compliance with regulatory standards

Determining and implementing continuous improvements in equipment and maintenance processes to improve efficiency and reliability

Collaborating with cross-functional teams to refine internal procedures and achieve optimized workflows

What we are looking for:

Equivalent experience in Electrical or System Engineering or a related field, including University Degree or equivalent experience, or vocational education (EFZ, FH, HF, BSc.)

Proven experience in the operation and maintenance of pharmaceutical plants or the biotech industry

Proficiency in SAP, COMOS (Plant Engineering Software), DeltaV (Process Control System), and MES Syncade (Manufacturing Execution System) is highly desirable

Proficient in English and/or German to competently communicate in our diverse, collaborative environment

Familiarity with GMP standards and protocols to ensure compliance in a regulated manufacturing setting

A self-reliant, trustworthy, and effective working approach that ensures successful completion of tasks and projects

Relocation assistance is available for eligible candidates and their families, ensuring a smooth transition to our welcoming community in Visp.

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.

Location. 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.

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 dependant on role and location.

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

What you'll do :

Carry out end to end Drug Product manufacturing under GMP: batch execution, documentation, troubleshooting, and review of results.

Complete and maintain all GMP documentation (batch records, logbooks, forms). Support process changes and CAPA activities.

Ensure every batch is made safely, on time, and according to quality and aseptic standards.

Set up, operate, and clean equipment for liquid and freeze dried (lyophilized) vial manufacturing.

Support compounding & formulations, buffer preparation, washing/autoclaving, filter integrity testing, filling/crimping, and visual inspection.

Experience with aseptic handling inside isolators or conventional cleanrooms, or work with single use components is a major plus.

Train colleagues and support cross functional teams with technical guidance.

Report equipment issues and support engineering teams with repairs in cleanroom/aseptic areas.

What we're looking for :

2-4 years of GMP shopfloor experience (ideally sterile Drug Product / Fill & Finish).

Drug Product experience is a strong advantage. EFZ apprenticeship (mechanic or similar: production mechanic, car mechanic, etc.) Also practical experience in professions with high hygiene and cleanliness requirements, such as cook/chef or comparable roles.

Good English skills for instructions and communication; German is a plus.

Familiarity with GMP, SOPs, and quality processes.

Reliable, well organized, team oriented working style.

IT knowledge (SAP/MES is a plus).

Willingness to support on call duties to some extent.

Currently operating in a 2 shift system; readiness for 3 shift work (regular 5 day week, occasional Saturday, no Sundays).

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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.

We are looking for a DeltaV Automation Engineer or Electrical Instrumentation & Control Engineer (m/f/d) to join us in a dynamic, cutting-edge environment where your work will significantly contribute to shaping the future of medicine.

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 dependant on role and location

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

What you will do:

Planning and realization of electrical MSR readiness (maintenance, changeovers, improvements) within the available budget and timelines

Ensuring seamless operation and flawless performance of high-automated Biologics facilities equipped with DeltaV and MES systems. Equivalent experience is also acceptable for educational requirements like MES

Managing GMP-compliant activities, including testing, documentation, and change management using systems such as Kneat and Ubik

Preparing and updating plant documentation in SAP/COMOS to ensure strict compliance with regulatory standards

Determining and implementing continuous improvements in equipment and maintenance processes to improve efficiency and reliability

Collaborating with cross-functional teams to refine internal procedures and achieve optimized workflows

What we are looking for:

Equivalent experience in Electrical or System Engineering or a related field, including University Degree or equivalent experience, or vocational education (EFZ, FH, HF, BSc.)

Proven experience in the operation and maintenance of pharmaceutical plants or the biotech industry

Proficiency in SAP, COMOS (Plant Engineering Software), DeltaV (Process Control System), and MES Syncade (Manufacturing Execution System) is highly desirable

Proficient in English and/or German to competently communicate in our diverse, collaborative environment

Familiarity with GMP standards and protocols to ensure compliance in a regulated manufacturing setting

A self-reliant, trustworthy, and effective working approach that ensures successful completion of tasks and projects

Relocation assistance is available for eligible candidates and their families, ensuring a smooth transition to our welcoming community in Visp.

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.