Nous sommes la société valaisanne appelée à devenir le leader suisse de la production hydroélectrique. Avec 130 collaboratrices et collaborateurs hautement qualifiés, nous contribuons activement à la transition énergétique et à la sécurité d'approvisionnement en électricité 100 % renouvelable, décarbonée et indigène au service du Valais et de la Suisse.

Pour la poursuite du développement de la centrale hydroélectrique valaisanne , FMV recherche de suite ou à convenir un/e

Chef/fe de projet aménagements hydroélectriques 80-100%

Dans ce rôle, vous travaillerez au sein du secteur support technique du département Production.

Votre mission

Votre mission est de gérer des projets et sous-projets de construction de nouvelles centrales hydroélectriques. Vous gérez les projets depuis l étude préliminaire jusqu à la phase de planification et de mise en œuvre. Vous dirigez et coordonnez des équipes de projet interdisciplinaires. Vous mandaterez et accompagnerez également des bureaux spécialisés externes.

Votre engagement dans vos projets contribuera à ce que le développement de l énergie hydraulique souhaité par le peuple Suisse, en particulier en vue du stockage de l énergie et de la production hivernale, puisse être réalisée étape par étape.

Votre profil

Master en génie civil (EPF ou FH) avec des connaissances spécialisées approfondies dans les domaines de l ingénierie hydraulique ou de la géotechniquePlus de 5 ans d expérience dans la planification et la mise en œuvre de structures hydrauliques ou souterrainesExpérience avérée en gestion de projet en tant planificateur, maître d ouvrage ou entrepreneurGrand intérêt pour d autres sujets pertinents aux projets hydroélectriques tels que l électromécanique, l environnement, l industrie de l énergie et les aspects légauxPersonnalité dynamique et flexible avec le désir d agir dans un environnement en constante évolutionCapacité à travailler à la fois de manière indépendante et en groupes de projet multidisciplinairesLangue maternelle allemande ou française avec une bonne connaissance de l autre langue (min. B1)

Pourquoi nous rejoindre ?

Une équipe ouverte et dynamique d ingénieurs et de scientifiques se réjouit de travailler avec vous. Votre taux d occupation est de 80 à 100 %. Votre lieu de travail est Sion ; en outre, des bureaux à Naters et Martigny sont également disponibles.

De plus, nous offrons :

Flexibilité et équilibre : temps de travail annualisé, 41 heures de travail hebdomadaire, jusqu'à 50 % de home-office.Conditions attractives : 5 semaines de congés, 14 jours fériés, 13e salaire, primes de jubilé chaque 5 ans, part variable sur des objectifs collectifs.Avantages sociaux : cotisations préférentielles à la caisse de pension, remboursement CFF tarif, prise en charge des cotisations aux assurances accidents et d indemnités journalières maladie.Développement professionnel : soutien à la formation, formations continues et perspectives de carrière à long terme.

Postulez dès maintenant ! Envoyez votre candidature via Jobup sous "Postuler rapidement". Nous nous réjouissons de vous lire !

Des questions ? Contactez les Ressources Humaines de FMV au ou par e-mail à .

jid10ae336ade jit1252ade 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