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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As CQV Engineer in the ADS Platform, Small Molecules you will manage existing systems in terms of qualification and supports investment projects, commissioning, and start-up activities in all aspects. You will also be responsible for the commissioning of current and future investment projects as well as the planning, coordination, execution, and documentation of all project-related qualification activities.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Asset life cycle management of existing systems with regard to qualification

Responsible for system qualification for new constructions, system expansions, and optimization of existing systems prior to GMP production

Responsible for coordinating technical change management

Support the qualification lead in all matters

Support Capex projects and the engineering team throughout various project phases as a member of the project organization

Coordinate interfaces and act as a link between engineering, commissioning, and qualification

Present and represent qualification during audits and inspections

Content review and completion of qualification activities performed

Ihre Hauptaufgaben

Asset Life Cycle Management von bestehenden Anlagen in Bezug auf Qualifizierung

Verantwortlich für Anlagenqualifizierung bei Neubauten / Anlageerweiterungen / Optimierung bestehender Anlagen vor einer GMP-Produktion

Zuständig für die Koordination des technischen Änderungswesens

Unterstützung des Qualifizierungsleiters in allen Belangen

Unterstützt Capex Projekte und das Engineering team in den verschiedenen Projektphasen als Mitglied der Projektorganisation

Koordiniert die Schnittstellen und agiert als Bindeglied zwischen Engineering, Inbetriebnahme / Qualifizierung

Vorstellen und vertreten der Qualifizierung während Audits und Inspektionen

Inhaltliche Kontrolle und Abschluss der durchgeführten Qualifizierungsarbeiten

What we are looking for

BSc or completed technical education in the field of mechanical, plant engineering, EMR or related field with several years of experience in process engineering, production, or a similar field

Ideally, good knowledge/experience in GMP

Several years of experience in active pharmaceutical ingredient (API) manufacturing in the chemical/pharmaceutical sector under GMP

Several years of experience in qualification

Enjoyment in creating and maintaining qualification documentation, which requires high standards of accuracy and cleanliness

Very good PC skills (MS Office / SAP / DMS / COMOS)

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.

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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As CQV Engineer in the ADS Platform, Small Molecules you will manage existing systems in terms of qualification and supports investment projects, commissioning, and start-up activities in all aspects. You will also be responsible for the commissioning of current and future investment projects as well as the planning, coordination, execution, and documentation of all project-related qualification activities.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Asset life cycle management of existing systems with regard to qualification

Responsible for system qualification for new constructions, system expansions, and optimization of existing systems prior to GMP production

Responsible for coordinating technical change management

Support the qualification lead in all matters

Support Capex projects and the engineering team throughout various project phases as a member of the project organization

Coordinate interfaces and act as a link between engineering, commissioning, and qualification

Present and represent qualification during audits and inspections

Content review and completion of qualification activities performed

Ihre Hauptaufgaben

Asset Life Cycle Management von bestehenden Anlagen in Bezug auf Qualifizierung

Verantwortlich für Anlagenqualifizierung bei Neubauten / Anlageerweiterungen / Optimierung bestehender Anlagen vor einer GMP-Produktion

Zuständig für die Koordination des technischen Änderungswesens

Unterstützung des Qualifizierungsleiters in allen Belangen

Unterstützt Capex Projekte und das Engineering team in den verschiedenen Projektphasen als Mitglied der Projektorganisation

Koordiniert die Schnittstellen und agiert als Bindeglied zwischen Engineering, Inbetriebnahme / Qualifizierung

Vorstellen und vertreten der Qualifizierung während Audits und Inspektionen

Inhaltliche Kontrolle und Abschluss der durchgeführten Qualifizierungsarbeiten

What we are looking for

BSc or completed technical education in the field of mechanical, plant engineering, EMR or related field with several years of experience in process engineering, production, or a similar field

Ideally, good knowledge/experience in GMP

Several years of experience in active pharmaceutical ingredient (API) manufacturing in the chemical/pharmaceutical sector under GMP

Several years of experience in qualification

Enjoyment in creating and maintaining qualification documentation, which requires high standards of accuracy and cleanliness

Very good PC skills (MS Office / SAP / DMS / COMOS)

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.

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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As CQV Engineer in the ADS Platform, Small Molecules you will manage existing systems in terms of qualification and supports investment projects, commissioning, and start-up activities in all aspects. You will also be responsible for the commissioning of current and future investment projects as well as the planning, coordination, execution, and documentation of all project-related qualification activities.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Asset life cycle management of existing systems with regard to qualification

Responsible for system qualification for new constructions, system expansions, and optimization of existing systems prior to GMP production

Responsible for coordinating technical change management

Support the qualification lead in all matters

Support Capex projects and the engineering team throughout various project phases as a member of the project organization

Coordinate interfaces and act as a link between engineering, commissioning, and qualification

Present and represent qualification during audits and inspections

Content review and completion of qualification activities performed

Ihre Hauptaufgaben

Asset Life Cycle Management von bestehenden Anlagen in Bezug auf Qualifizierung

Verantwortlich für Anlagenqualifizierung bei Neubauten / Anlageerweiterungen / Optimierung bestehender Anlagen vor einer GMP-Produktion

Zuständig für die Koordination des technischen Änderungswesens

Unterstützung des Qualifizierungsleiters in allen Belangen

Unterstützt Capex Projekte und das Engineering team in den verschiedenen Projektphasen als Mitglied der Projektorganisation

Koordiniert die Schnittstellen und agiert als Bindeglied zwischen Engineering, Inbetriebnahme / Qualifizierung

Vorstellen und vertreten der Qualifizierung während Audits und Inspektionen

Inhaltliche Kontrolle und Abschluss der durchgeführten Qualifizierungsarbeiten

What we are looking for

BSc or completed technical education in the field of mechanical, plant engineering, EMR or related field with several years of experience in process engineering, production, or a similar field

Ideally, good knowledge/experience in GMP

Several years of experience in active pharmaceutical ingredient (API) manufacturing in the chemical/pharmaceutical sector under GMP

Several years of experience in qualification

Enjoyment in creating and maintaining qualification documentation, which requires high standards of accuracy and cleanliness

Very good PC skills (MS Office / SAP / DMS / COMOS)

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.

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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As CQV Engineer in the ADS Platform, Small Molecules you will manage existing systems in terms of qualification and supports investment projects, commissioning, and start-up activities in all aspects. You will also be responsible for the commissioning of current and future investment projects as well as the planning, coordination, execution, and documentation of all project-related qualification activities.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Asset life cycle management of existing systems with regard to qualification

Responsible for system qualification for new constructions, system expansions, and optimization of existing systems prior to GMP production

Responsible for coordinating technical change management

Support the qualification lead in all matters

Support Capex projects and the engineering team throughout various project phases as a member of the project organization

Coordinate interfaces and act as a link between engineering, commissioning, and qualification

Present and represent qualification during audits and inspections

Content review and completion of qualification activities performed

Ihre Hauptaufgaben

Asset Life Cycle Management von bestehenden Anlagen in Bezug auf Qualifizierung

Verantwortlich für Anlagenqualifizierung bei Neubauten / Anlageerweiterungen / Optimierung bestehender Anlagen vor einer GMP-Produktion

Zuständig für die Koordination des technischen Änderungswesens

Unterstützung des Qualifizierungsleiters in allen Belangen

Unterstützt Capex Projekte und das Engineering team in den verschiedenen Projektphasen als Mitglied der Projektorganisation

Koordiniert die Schnittstellen und agiert als Bindeglied zwischen Engineering, Inbetriebnahme / Qualifizierung

Vorstellen und vertreten der Qualifizierung während Audits und Inspektionen

Inhaltliche Kontrolle und Abschluss der durchgeführten Qualifizierungsarbeiten

What we are looking for

BSc or completed technical education in the field of mechanical, plant engineering, EMR or related field with several years of experience in process engineering, production, or a similar field

Ideally, good knowledge/experience in GMP

Several years of experience in active pharmaceutical ingredient (API) manufacturing in the chemical/pharmaceutical sector under GMP

Several years of experience in qualification

Enjoyment in creating and maintaining qualification documentation, which requires high standards of accuracy and cleanliness

Very good PC skills (MS Office / SAP / DMS / COMOS)

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.

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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As CQV Engineer in the ADS Platform, Small Molecules you will manage existing systems in terms of qualification and supports investment projects, commissioning, and start-up activities in all aspects. You will also be responsible for the commissioning of current and future investment projects as well as the planning, coordination, execution, and documentation of all project-related qualification activities.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Asset life cycle management of existing systems with regard to qualification

Responsible for system qualification for new constructions, system expansions, and optimization of existing systems prior to GMP production

Responsible for coordinating technical change management

Support the qualification lead in all matters

Support Capex projects and the engineering team throughout various project phases as a member of the project organization

Coordinate interfaces and act as a link between engineering, commissioning, and qualification

Present and represent qualification during audits and inspections

Content review and completion of qualification activities performed

Ihre Hauptaufgaben

Asset Life Cycle Management von bestehenden Anlagen in Bezug auf Qualifizierung

Verantwortlich für Anlagenqualifizierung bei Neubauten / Anlageerweiterungen / Optimierung bestehender Anlagen vor einer GMP-Produktion

Zuständig für die Koordination des technischen Änderungswesens

Unterstützung des Qualifizierungsleiters in allen Belangen

Unterstützt Capex Projekte und das Engineering team in den verschiedenen Projektphasen als Mitglied der Projektorganisation

Koordiniert die Schnittstellen und agiert als Bindeglied zwischen Engineering, Inbetriebnahme / Qualifizierung

Vorstellen und vertreten der Qualifizierung während Audits und Inspektionen

Inhaltliche Kontrolle und Abschluss der durchgeführten Qualifizierungsarbeiten

What we are looking for

BSc or completed technical education in the field of mechanical, plant engineering, EMR or related field with several years of experience in process engineering, production, or a similar field

Ideally, good knowledge/experience in GMP

Several years of experience in active pharmaceutical ingredient (API) manufacturing in the chemical/pharmaceutical sector under GMP

Several years of experience in qualification

Enjoyment in creating and maintaining qualification documentation, which requires high standards of accuracy and cleanliness

Very good PC skills (MS Office / SAP / DMS / COMOS)

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.

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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

The Utility & Infrastructure Specialist is responsible for the technical and organizational management of all clean and black utilities, as well as HVAC systems. They ensure the proper operation and monitoring of systems such as clean steam, purified water (PW), and HVAC, in compliance with GMP requirements and occupational safety guidelines.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Responsible for the proper operation and availability of clean and black utility systems

Monitoring, management, and organization of continuous monitoring of purified media systems

Together with the cleaning coordinator, responsible for organizing and performing cleaning before start-up and after campaign completion, as well as restoring the system

Handling deviations in collaboration with QA, QC, and operations; defining appropriate measures and preparing monthly reports

Coordinating interfaces with operations, engineering, QA, and QC

Responsible for all media in the black area, waste management, and proper disposal of liquid and solid waste

Planning waste streams for new products, partnering with production and the environmental lab

Pump inspections, sampling of PW water, SIWAKO, management of storage materials / overgarments, support in infrastructure system maintenance and monitoring

Ihre Hauptaufgaben

Verantwortlich für den ordnungsgemässen Betrieb und die Verfügbarkeit der Clean- und Black-Utilities Anlagen

Kontrolle, Betreuung und Organisation des fortlaufenden Monitorings der Reinst Medien Systeme

Ist gemeinsam mit dem Reinigungsverantwortlichen für die Organisation und Durchführung der Reinigung vor dem Einfahren sowie für die Reinigung nach Kampagnenende und die Rückerstellung der Anlage verantwortlich

Bearbeitung entstandener Abweichungen in Zusammenarbeit mit QA, QC und dem Betrieb. Definition entsprechender Massnahmen und Erstellung der Monatsberichte

Koordination der Schnittstellen zum Betrieb, dem Betriebsengineering sowie QA und QC

Verantwortung für alle Medien im Schwarzbereich, Abfallmanagement, korrekte Entsorgung der anfallenden Flüssig- und Feststoffabfällen

Planung der Abfallströme bei neuen Produkten, Partner mit Produktion und Umweltlabor

Pumpenkontrollen, Bemusterung des WP-Wassers, SIWAKO, Bewirtschaftung des Lagermaterials / Überkleider, Unterstützung bei Infra Anlagen im Unterhalt, sowie dessen Überwachung

What we are looking for

Bachelor or completed technical education in Process Engineering, Mechanical, EMR, Chemical Engineering, or a related field

In-depth technical knowledge in CQ and OPs , possibly in the biological, chemical and/or pharmaceutical industry

Extended EHS knowledge

Experience with utilities/HVAC

Solid internal and external collaboration and the ability to lead diverse teams in the successful delivery of projects.

Experience at working both independently and in a team-oriented, collaborative environment is essential.

Can conform to shifting priorities, demands and timelines through analytical and problem-solving capabilities.

Ability to effectively prioritize and execute tasks in a fast-paced environment.

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.

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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As CQV Engineer in the ADS Platform, Small Molecules you will manage existing systems in terms of qualification and supports investment projects, commissioning, and start-up activities in all aspects. You will also be responsible for the commissioning of current and future investment projects as well as the planning, coordination, execution, and documentation of all project-related qualification activities.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Asset life cycle management of existing systems with regard to qualification

Responsible for system qualification for new constructions, system expansions, and optimization of existing systems prior to GMP production

Responsible for coordinating technical change management

Support the qualification lead in all matters

Support Capex projects and the engineering team throughout various project phases as a member of the project organization

Coordinate interfaces and act as a link between engineering, commissioning, and qualification

Present and represent qualification during audits and inspections

Content review and completion of qualification activities performed

Ihre Hauptaufgaben

Asset Life Cycle Management von bestehenden Anlagen in Bezug auf Qualifizierung

Verantwortlich für Anlagenqualifizierung bei Neubauten / Anlageerweiterungen / Optimierung bestehender Anlagen vor einer GMP-Produktion

Zuständig für die Koordination des technischen Änderungswesens

Unterstützung des Qualifizierungsleiters in allen Belangen

Unterstützt Capex Projekte und das Engineering team in den verschiedenen Projektphasen als Mitglied der Projektorganisation

Koordiniert die Schnittstellen und agiert als Bindeglied zwischen Engineering, Inbetriebnahme / Qualifizierung

Vorstellen und vertreten der Qualifizierung während Audits und Inspektionen

Inhaltliche Kontrolle und Abschluss der durchgeführten Qualifizierungsarbeiten

What we are looking for

BSc or completed technical education in the field of mechanical, plant engineering, EMR or related field with several years of experience in process engineering, production, or a similar field

Ideally, good knowledge/experience in GMP

Several years of experience in active pharmaceutical ingredient (API) manufacturing in the chemical/pharmaceutical sector under GMP

Several years of experience in qualification

Enjoyment in creating and maintaining qualification documentation, which requires high standards of accuracy and cleanliness

Very good PC skills (MS Office / SAP / DMS / COMOS)

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.

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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As CQV Engineer in the ADS Platform, Small Molecules you will manage existing systems in terms of qualification and supports investment projects, commissioning, and start-up activities in all aspects. You will also be responsible for the commissioning of current and future investment projects as well as the planning, coordination, execution, and documentation of all project-related qualification activities.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Asset life cycle management of existing systems with regard to qualification

Responsible for system qualification for new constructions, system expansions, and optimization of existing systems prior to GMP production

Responsible for coordinating technical change management

Support the qualification lead in all matters

Support Capex projects and the engineering team throughout various project phases as a member of the project organization

Coordinate interfaces and act as a link between engineering, commissioning, and qualification

Present and represent qualification during audits and inspections

Content review and completion of qualification activities performed

Ihre Hauptaufgaben

Asset Life Cycle Management von bestehenden Anlagen in Bezug auf Qualifizierung

Verantwortlich für Anlagenqualifizierung bei Neubauten / Anlageerweiterungen / Optimierung bestehender Anlagen vor einer GMP-Produktion

Zuständig für die Koordination des technischen Änderungswesens

Unterstützung des Qualifizierungsleiters in allen Belangen

Unterstützt Capex Projekte und das Engineering team in den verschiedenen Projektphasen als Mitglied der Projektorganisation

Koordiniert die Schnittstellen und agiert als Bindeglied zwischen Engineering, Inbetriebnahme / Qualifizierung

Vorstellen und vertreten der Qualifizierung während Audits und Inspektionen

Inhaltliche Kontrolle und Abschluss der durchgeführten Qualifizierungsarbeiten

What we are looking for

BSc or completed technical education in the field of mechanical, plant engineering, EMR or related field with several years of experience in process engineering, production, or a similar field

Ideally, good knowledge/experience in GMP

Several years of experience in active pharmaceutical ingredient (API) manufacturing in the chemical/pharmaceutical sector under GMP

Several years of experience in qualification

Enjoyment in creating and maintaining qualification documentation, which requires high standards of accuracy and cleanliness

Very good PC skills (MS Office / SAP / DMS / COMOS)

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.

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 local tailored benefits can also be found below.

Benefits in Visp:

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As CQV Engineer in the ADS Platform, Small Molecules you will manage existing systems in terms of qualification and supports investment projects, commissioning, and start-up activities in all aspects. You will also be responsible for the commissioning of current and future investment projects as well as the planning, coordination, execution, and documentation of all project-related qualification activities.

The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role involves being onsite full time.

What you will do

Asset life cycle management of existing systems with regard to qualification

Responsible for system qualification for new constructions, system expansions, and optimization of existing systems prior to GMP production

Responsible for coordinating technical change management

Support the qualification lead in all matters

Support Capex projects and the engineering team throughout various project phases as a member of the project organization

Coordinate interfaces and act as a link between engineering, commissioning, and qualification

Present and represent qualification during audits and inspections

Content review and completion of qualification activities performed

Ihre Hauptaufgaben

Asset Life Cycle Management von bestehenden Anlagen in Bezug auf Qualifizierung

Verantwortlich für Anlagenqualifizierung bei Neubauten / Anlageerweiterungen / Optimierung bestehender Anlagen vor einer GMP-Produktion

Zuständig für die Koordination des technischen Änderungswesens

Unterstützung des Qualifizierungsleiters in allen Belangen

Unterstützt Capex Projekte und das Engineering team in den verschiedenen Projektphasen als Mitglied der Projektorganisation

Koordiniert die Schnittstellen und agiert als Bindeglied zwischen Engineering, Inbetriebnahme / Qualifizierung

Vorstellen und vertreten der Qualifizierung während Audits und Inspektionen

Inhaltliche Kontrolle und Abschluss der durchgeführten Qualifizierungsarbeiten

What we are looking for

BSc or completed technical education in the field of mechanical, plant engineering, EMR or related field with several years of experience in process engineering, production, or a similar field

Ideally, good knowledge/experience in GMP

Several years of experience in active pharmaceutical ingredient (API) manufacturing in the chemical/pharmaceutical sector under GMP

Several years of experience in qualification

Enjoyment in creating and maintaining qualification documentation, which requires high standards of accuracy and cleanliness

Very good PC skills (MS Office / SAP / DMS / COMOS)

Fluent in German and good level of English.

Why Lonza ?

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.

Inclusion is one of Lonza's four core values, alongside integrity, innovation, and initiative. We understand the value of our differences and the benefits they bring to our company, community, and culture. We also recognize the value of every person's contribution, regardless of characteristics, preferences, and beliefs - including race, color, ethnicity, sexual orientation, gender identity, and religion.