Placé.e sous l'autorité directe du Responsable de service et basé à Prilly, vous assurez les missions suivantes : Chargé d'études CVC (H/F) A propos d'EQUANS
EQUANS soutient les entreprises dans la conception, la réalisation et l'exploitation de leurs bâtiments, sites et infrastructures de façon efficiente et prévoyante. Grâce à nos compétences en techniques et automation du bâtiment (CVCR, froid industriel et électricité), facility management, transformation énergétique, numérisation et maintenance & exploitation industrielle nous proposons des solutions sur l'ensemble du cycle de vie des bâtiments. Nous permettons ainsi une exploitation fiable 24 heures sur 24 et relevons avec nos clients les enjeux de la transition énergétique.

En Suisse, nous travaillons avec nos 7'000 collègues dans plus de 140 succursales. Dans le monde entier, le groupe EQUANS emploie 90'000 personnes dans 17 pays. Placé.e sous l'autorité directe du Responsable de service et basé à Prilly, vous assurez les missions suivantes : Chargé d'études CVC (H/F) Vos missions Vous procédez à l'élaboration technique d'un "projet" d'ouvrage ou d'installation HVAC :Vous proposez une solution technique globale,Vous réalisez les schémas de principe et les dimensionnements des équipements et des réseaux,Vous rédigez les demandes d'autorisation et les descriptifs techniques,Vous établissez le prix de revient du budget estimatif de l'avant-projet au chiffrage du cahier de soumission,Vous assurez le suivi de l'offre et des demandes complémentaires auprès du client,Vous gérez les interfaces entre les services et les éventuels co-traitants pour mener à bien votre étude,Vous êtes responsable de l'organisation de votre étude et du respect des délais de remise de document ou de remise d'offre,Vous êtes l'interlocuteur privilégié du client pendant la phase d'étude et de chiffrage.Vous assurez la passation auprès du chargé d'affaires pour l'exécution.Vous réalisez des devis en direct sur demande du client, allant d'une petite modification d'installation à la proposition complète d'un nouveau concept,Vous intervenez principalement dans le secteur industriel,Vous réalisez les chiffrages de soumissions privées ou publiques et êtes capable de proposer des solutions techniques alternatives,Vous assurez la passation des dossiers commerciaux aux chargés d'affaires,Vous travaillez sur des sujets multiples en simultanée,Vous connaissez et respectez les normes et règlements de la profession et intervenez en soutien aux opérationnels,Basé.e à Prilly, vous êtes amené à traiter des projets dans l'ensemble des cantons Romand. Votre profil d'une formation supérieure en génie climatique ou équivalente, vous avez une expérience de 3 ans minimum dans le domaine des études CVC en Suisse.Votre esprit d'analyse et de synthèse ainsi que votre rigueur, vous permettent de dimensionner et chiffrer avec précision.Vous êtes capable de gérer plusieurs projets en simultanée.Vous aimez aller sur site pour comprendre le fonctionnement des installations et proposer des modifications.Vous vous distinguez de par votre esprit d'équipe, votre sens de l'initiative et votre orientation client.Enfin, vous maitrisez parfaitement les outils informatiques. Vos perspectives Carrière
Des opportunités de carrière diversifiées Opportunités internationales Formation continue
Programme de formation interne polyvalent Financement de diverses formations externes Formation professionnelle
"Topentreprise formatrice" certifiée dans le domaine de la technique du bâtiment Questions sociales
Bonnes prestations sociales (caisse de retraite, maladie, accident, etc.) Global
Présent dans 20 pays et sur plus de 140 sites en Suisse Transition énergétique
Leader de la fourniture de solutions globales pour le bâtiment et l'énergie en Suisse Vous trouverez plus d'informations sur EQUANS en tant qu'employeur ici . Ton lieu de travail En cas d'intérêt, nous vous invitons à postuler en envoyant votre dossier complet.

Rejoignez nos équipes et devenez un acteur de l'aventure EQUANS Switzerland SA ! Postuler en ligne Agence de placement jidd6c4106ade jit1249ade jpiy25ade weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

For our successful and growing Drug Product focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Global MSAT DP Qualification & Validation Lead position.

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 Stein:

What you will do:

Lead global process control strategy for drug product manufacturing

Own global strategies for equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV)

Define and govern global SOPs, standards, templates, and tools aligned with regulations and best practice

Own qualification strategy for key unit operations: thawing, compounding, filling, lyophilization, and crimping

Guide Tech Transfer and local MSAT teams on validation strategies, scale up, and sampling plans

Review and approve validation documentation; analyze production data using appropriate statistical methods

Act as subject matter expert during health authority inspections on validation and CPV/OPV

What we are looking for:

Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field; or equivalent experience

Expertise in equipment qualification for aseptic drug product manufacturing

Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats

Proven experience with regulatory submissions and pre approval inspections

Strong statistical skills for qualification, validation, and CPV; Data Science certification or Lean Six Sigma Black Belt preferred

Knowledge of risk assessment, deviation management, change control, and root cause analysis

Excellent English communication, documentation, leadership, and cross functional collaboration skills

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.

weniger ansehen