Location: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.
For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.
What you will get:
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
A variety of benefits dependant on role and location
The full list of our global benefits can be also found on .
What you will do:
Drive process standardization and efficiency in line with Lonza's LBMS standards
Support the implementation of a Lean Batch Release program on site
Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes
Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality
Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope
Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines
Share best practice within the Visp Site as well as with the wider Lonza Pharma network
What we are looking for:
University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)
Profound experience in a GMP regulated environment; preferably within QA/QC
Experience with Lean / Six Sigma, within a Quality related environment
Certified Green Belt or higher is required
PowerBI and/or Minitab knowledge would be an advantage
Fluent German (written and verbal) and good English language skills are required
Strong ability to collaborate effectively with colleagues across different functions
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
weniger ansehenLocation: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.
For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.
What you will get:
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
A variety of benefits dependant on role and location
The full list of our global benefits can be also found on .
What you will do:
Drive process standardization and efficiency in line with Lonza's LBMS standards
Support the implementation of a Lean Batch Release program on site
Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes
Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality
Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope
Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines
Share best practice within the Visp Site as well as with the wider Lonza Pharma network
What we are looking for:
University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)
Profound experience in a GMP regulated environment; preferably within QA/QC
Experience with Lean / Six Sigma, within a Quality related environment
Certified Green Belt or higher is required
PowerBI and/or Minitab knowledge would be an advantage
Fluent German (written and verbal) and good English language skills are required
Strong ability to collaborate effectively with colleagues across different functions
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
weniger ansehenLocation: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.
For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.
What you will get:
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
A variety of benefits dependant on role and location
The full list of our global benefits can be also found on .
What you will do:
Drive process standardization and efficiency in line with Lonza's LBMS standards
Support the implementation of a Lean Batch Release program on site
Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes
Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality
Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope
Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines
Share best practice within the Visp Site as well as with the wider Lonza Pharma network
What we are looking for:
University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)
Profound experience in a GMP regulated environment; preferably within QA/QC
Experience with Lean / Six Sigma, within a Quality related environment
Certified Green Belt or higher is required
PowerBI and/or Minitab knowledge would be an advantage
Fluent German (written and verbal) and good English language skills are required
Strong ability to collaborate effectively with colleagues across different functions
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
weniger ansehenAssociate Director, Technical Sales
Location: Visp with Relocation and Visa support is to be offered
Today, Lonza is a global leader in life sciences operating across five continents.
As an Associate Director, Technical Sales, you will help guide customers toward the best technical and commercial solutions across Lonza's platforms. In this role, you will use your scientific expertise and strategic mindset to shape high value opportunities, collaborate with global teams, and contribute directly to the growth of our business.
What you will get
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
A variety of benefits dependent on role and location
The full list of our global benefits can be found here:
What you will do
Lead integrated offer development for Advanced Synthesis and represent the platform in global strategic initiatives.
Manage a global team of technical sales professionals and support their growth and performance.
Improve processes, tools, and templates used to create integrated offers for ADCs and XDCs.
Contribute to preparing contract templates, including terms, conditions, and master service agreements.
Ensure accurate costing and proposal inputs using approved tools and methods.
Collaborate with cross functional teams to build executable, customer focused proposals.
Support customer engagements by preparing proposals, leading discussions, and participating in evaluations.
What we are looking for
Preferably PHD or a MSc in a scientific field or equivalent relevant experience.
Fluency in English; German language skills are an advantage.
10+ years of experience in the pharmaceutical or biotech industry.
Proven experience leading and developing teams.
Strong understanding of integrated services and manufacturing processes.
Excellent communication, analytical thinking, and collaborative skills.
Knowledge of CDMO operations and Lonza's cross platform offerings.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
weniger ansehenThe actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
Join our team to translate process requirements into clean, efficient MES, while continuously identifying optimization opportunities across system interfaces. You'll collaborate closely with MES management, process owners, and cross functional partners to enhance data flows and further develop integrations with ERP, LIMS, and automation systems. If you enjoy combining process know how with hands on programming to improve manufacturing workflows, this role is for you. Check out Your Career in Drug Product Services at Lonza
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:
Work closely with MES manager, system users and process owners to develop and revise MES recipes in a timely manner using Typescript
Configure production recipes using a library of objects and manage MES master data like Products, Locations, Equipment, Materials
Assist in fulfilling requirements of quality records such as process change controls, CAPA and deviations
Draft and execute test script for the validation of recipes (IQ, OQ, PQ)
Establishment and further development of interfaces to other systems such as ERP, LIMS and automation and work closely with this departments
Development of concepts for an optimal data flow with the interfaces, taking into account all use cases. Definition of requirements for the MES system for its further development
Support production via the Helpdesk, assisting with production issues
What we are looking for:
Proven experience with MES in a programming/modeling capacity (not only as an end user). Previous exposure to any of the commercial MES systems (Rockwell PharmaSuite, Werum Pas-X, POMS, Emerson Syncade)
GMP manufacturing experience is a must (specifically Fill & Finish or sterile/aseptic manufacturing is a plus)
Academic degree (e.g. in IT) is an advantage
Programming experience is a must. Hands on TypeScript experience is a plus
You enjoy working cross-functionally, communicating with various stakeholders and you enjoy looking for ways to optimize processes.
Fluent English; German is a plus and willingness to learn is expected.
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 ansehenLocation: Stein, AG (Switzerland)
Relocation assistance is available for eligible candidates and their families, if needed.
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!
Join us as a Visual Inspection Engineer and be part of an exciting Greenfield project! As part of our Lonza Drug Product Services department, you will lead the introduction of two cutting-edge automated visual inspection lines and develop structured recipe strategies to ensure flawless production. This is your chance to shape the future of advanced manufacturing from the ground up
What you'll get:
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
Along with competitive salaries, you'll find a wide range of lifestyle, family and leisure benefits available. The full list of our local benefits can be also found on assetstream.aspx
What you'll do:
Bring two new automated visual inspection lines into production
Develop a structured recipe development approach for a complex and evolving product portfolio (vial liquid, lyophilized, and pre-filled syringes). Establish a systematic and automated approach for recipe development and change control to reduce technical transfer time in AVI.
Execute and support recipe validation and qualification, including all relevant documentation.
Develop a LEAN approach for recipe development to support a complex product portfolio (vial liquid, lyophilized, and pre-filled syringes). Act as a key partner in ensuring a cost-efficient visual inspection (VI) department through continuous recipe improvement, leading to lower eject rates (gray) and false reject rates (FRR).
Implement image and video databases, along with data visualization, to support continuous improvement and future AI integration.
Support or lead innovation efforts, including the future implementation of virtual PQ and an artificial intelligence (AI) layer in existing AVI systems
What we're looking for:
Masters or PhD in Life Science, Engineering, Computer Vision or equivalent experience
Several years of experience either in the pharmaceutical GMP-controlled environment OR with visual inspection systems intended for the pharmaceutical industry
S trong technical knowledge of automated visual inspection (AVI) and 100% camera in-process control (IPC) in filling lines, e.g., crimping quality
Strong technical knowledge of optical systems for troubleshooting, including cameras, lenses, and lighting.
Experience in developing new recipes in AVI, including experience in recipe qualification and validation
You enjoy working independently in a highly dynamic environment
Fluency in English (knowledge of German is a plus)
Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
weniger ansehenLocation: The actual location of this job is in Visp, Switzerland. Hybrid Work Model is applicable. Relocation assistance is available for eligible candidates and their families, if needed.
For our site in Visp we are currently looking for a Senior Quality Excellence Manager (m/f/d), who will become part of our Quality Excellence team. In this role, you will drive operational excellence at its best and contribute as a strong influential LEAN specialist within a matrix organization to support our Quality organization on its way to best in class performance.
What you will get:
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
A variety of benefits dependant on role and location
The full list of our global benefits can be also found on .
What you will do:
Drive process standardization and efficiency in line with Lonza's LBMS standards
Support the implementation of a Lean Batch Release program on site
Establish Quality Excellence CoE and PMO structures, supporting the standardization, simplification and digitalization of our key quality processes
Facilitate to embed a LEAN culture of continuous improvement and ideation within Quality
Monitor and enable reporting of Quality performance KPIs for our site in Visp and initiate necessary activities to enable target achievement by the departments in scope
Support multi-disciplinary project teams and hold team members accountable to achieve the project goals within given timelines
Share best practice within the Visp Site as well as with the wider Lonza Pharma network
What we are looking for:
University Degree in a scientific area OR an absolved apprenticeship in a pharmaceutical environment (e.g. Lab Technician, CPT, etc)
Profound experience in a GMP regulated environment; preferably within QA/QC
Experience with Lean / Six Sigma, within a Quality related environment
Certified Green Belt or higher is required
PowerBI and/or Minitab knowledge would be an advantage
Fluent German (written and verbal) and good English language skills are required
Strong ability to collaborate effectively with colleagues across different functions
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
weniger ansehenDer Ort dieser Stelle befindet sich in Stein, AG, Schweiz. Berechtigten Bewerbern und ihren Familien steht bei Bedarf Unterstützung beim Umzug zur Verfügung.
Du rüstest unsere Anlagen um, behebst kleinere Störungen und hältst so die Produktion zuverlässig am Laufen. In der GMP gerechten Abfüllung (Fill & Finish) arbeitest du im Reinraum und im 2 Schichtmodell. Dich erwartet ein eingespieltes, wertschätzendes Team, in dem Zusammenarbeit wirklich zählt. Lerne unsere Manufacturing Operations kennen - Your Career in Manufacturing Operations at Lonza !
Was auf dich wartet:
Eine agile Karriere und eine dynamische Arbeitskultur.
Ein integratives und ethisches Arbeitsumfeld
Vergütungsprogramme, die hohe Leistung anerkennen.
Neben einem wettbewerbsfähigen Gehalt erwarten Sie zahlreiche Vorteile für Lifestyle, Familie und Freizeit. Unsere vollständige Liste der lokalen Benefits finden Sie unten:
Benefits in Stein:
Deine Aufgaben:
Du meisterst alle Arbeiten im Isolator - inklusive qualifizierter Eingriffe, Filtertests sowie Be und Entladen des Gefriertrockners.
Du rüstest Abfüll und Produktionsanlagen auf und ab, bereitest Räume & Equipment vor und übernimmst Reinigungs und GMP gerechte Dokumentationstätigkeiten.
Du führst mechanische und technische Aufgaben im Reinraum durch, installierst und de-installierst Equipment und übernimmst technische Verantwortung für Anlagen.
Du überwachst Produktionsprozesse, führst IPCs und mikrobiologisches Monitoring durch und erkennst Abweichungen sofort.
Du unterstützt bei Fehleranalysen, löst komplexe Fragestellungen und agierst als Spezialist in sowie Ansprechperson an der Abfülllinie.
Du gestaltest den Bereich aktiv mit, bildest neue Mitarbeitende aus, organisierst vorbeugende Instandhaltung und förderst kontinuierliche Prozessverbesserungen.
Was wir suchen:
Mechanische Grundausbildung, z. B. als KFZ Mechanikerin, Anlagenmechanikerin oder in einem vergleichbaren technischen Beruf.
Erste Berufserfahrung als Linienmechaniker in oder in einer ähnlichen technischen Funktion ist wünschenswert.
Erfahrung im Reinraum sowie Arbeiten nach GMP Standards sind ein grosses Plus.
Erfahrung in der Pharmaproduktion, idealerweise an Fill & Finish Anlagen, ist von Vorteil.
Fliessende Deutschkenntnisse; Englischkenntnisse sind ein Plus.
Bereitschaft zur Arbeit im 2 Schichtmodell, sowie Bereitschaft im Reinraum zu arbeiten.
Über Lonza
Bei Lonza sind unsere Mitarbeiter unsere größte Stärke. An über 30 Standorten auf fünf Kontinenten arbeiten unsere global vernetzten Teams täglich zusammen, um die Medikamente von morgen herzustellen. Unsere Grundwerte: Zusammenarbeit, Verantwortlichkeit, Exzellenz, Leidenschaft und Integrität spiegeln wider, wer wir sind und wie wir zusammenarbeiten. Die Ideen jedes Einzelnen, ob groß oder klein, haben das Potenzial, Millionen von Leben zu verbessern, und genau daran möchten wir Sie teilhaben lassen.
Innovation gedeiht, wenn Menschen unterschiedlichster Herkunft ihre einzigartigen Perspektiven einbringen. Bei Lonza schätzen wir Vielfalt und setzen uns für ein integratives Umfeld für alle Mitarbeiter ein. Wenn Sie bereit sind, die bahnbrechenden Ideen unserer Kunden in praktikable Therapien umzusetzen, freuen wir uns, Sie an Bord begrüßen zu dürfen.
Bereit die Zukunft der Life Sciences zu gestalten? Jetzt bewerben
weniger ansehenThe actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
In this role you will have the opportunity to lead a business critical visual inspection and container closure integrity testing team at the heart of Drug Product Services. With full technical ownership across automated, semi automated, and manual visual inspection processes, you will partner closely with customers, health authorities, and cross functional teams to deliver safe, compliant, and high quality outcomes. You will lead and develop a fast growing expert team, driving innovation and successfully scaling next generation inspection technologies as part of an exciting growth project.
Check out Your Career in Drug Product Services at Lonza !
What you will get:
An agile career and a dynamic work culture.
A highly collaborative environment that fosters teamwork and inclusion.
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:
Manage a team of a Vision Engineers, Process Experts and Operators with responsibility for all aspects of people leadership such as development, coaching, hiring and disciplinary topics. Maintain a culture of empowerment and innovation, trust, high performance and change readiness.
Technical system ownership: Provide scientific leadership to the team and other functions to ensure visual inspection processes are executed timely, cost effective and with the highest quality. Proactively anticipate, evaluate and resolve technical challenges and enables innovation.
Responsible for operative takeover of the automated, semi-automated, manual visual inspection and container closure integrity testing
Manage the customer interface in technical client visits and adapt technical capabilities in order to meet the customer requirements. Represent the facility during regulatory inspections and audits of clients and health authorities.
Accountable for safety, compliance and regulatory aspects. Preparation of risk analysis and all relevant procedures to ensure regulatory compliance and achieve business goals.
Support of the project team regarding complex topics by use of scientific and statistical knowledge.
Ensure and manage the interfaces between CAPEX team, Manufacturing, Plant Engineering, Automation, Support, QC and QA. Collaborate with functions in the project and across Drug Product Services, especially the existing drug product facilities)
Support the Senior Director Operational Lead of one of our largest growth project (Dolphin) in developing, prioritizing and achieving goals with respect to the project and overall DPS (Drug Product Services) goals. Ensure a good information exchange from the management level to the organization and the other way around through regularly team meetings and clear communication.
What we are looking for:
Extensive experience in visual inspection of parenteral drug product (specifically vials and syringes) in a GMP environment is a must. Broad experience with various different visual inspection systems such as manual, semi-automatic or AVI is an advantage.
Team leadership experience is a prerequisite
Experience with audits of health authorities
Fluency in English is a must (fluency in German is an advantage) with strong communication skills with stakeholders from various functions and levels.
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 ansehenSofern erforderlich, steht berechtigten Kandidaten und ihren Familien Unterstützung beim Umzug zur Verfügung.
Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen. Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen. Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig. Denn ihre Ideen, ob gross und klein, verbessern die Welt. Und das ist die Art von Arbeit, an der wir Teil haben möchten.
Zur Verstärkung des Teams am Standort Visp wird eine erfahrene Persönlichkeit für die fachliche Leitung eines EMR-Subteams gesucht. Im Fokus stehen Projektierung, Instandhaltung, Dokumentation, Know-how-Transfer sowie die Einhaltung von GMP- und Sicherheitsvorschriften.
Was wir dir bieten:
Eine agile Karriere und eine dynamische Arbeitskultur
Einen integrativen und ethischen Arbeitsplatz
Vergütungsprogramme, die hohe Leistung anerkennen
Neben einem wettbewerbsfähigen Gehalt erwarten dich zahlreiche Vorteile in den Bereichen Lifestyle, Familie und Freizeit. Die vollständige Liste unserer globalen Leistungen findest du auch unter:
Deine Aufgaben:
Planung und Umsetzung von Automatisierungsprojekten (Anlagenoptimierungen, Erweiterungen, Produkteumstellungen)
Technische Verantwortung über alle Projektphasen - von der Konzeption bis zur Inbetriebnahme
Mitarbeit in interdisziplinären Projektteams sowie Teilnahme an Risikoanalysen und Betriebsversuchen
Sicherstellung einer zuverlässigen, wirtschaftlichen Instandhaltung im GMP-regulierten Umfeld
Koordination von internen und externen Partnern sowie Überwachung des Instandhaltungsbudgets
Pflege und laufende Aktualisierung der Anlagendokumentation (SAP, COMOS)
Verantwortung für GMP-gerechtes Änderungsmanagement und Systempflege
Fachliche Betreuung definierter EMR-Bereiche sowie Weitergabe von Know-how an Werkstatt- und Betriebspersonal
Einhaltung und Umsetzung geltender GMP-, Sicherheits- und Umweltvorgaben
Dein Profil:
Abgeschlossenes Studium als Ingenieur in (ETH, FH, HF) in Elektro-, Automations- oder Systemtechnik
Mehrjährige Erfahrung im Betrieb, in der Instandhaltung oder im Anlagenbau in einem GMP-regulierten Umfeld
Kenntnisse in SAP, COMOS, DeltaV, MES von Vorteil
Sehr gute Deutschkenntnisse in Wort und Schrift, gute Englischkenntnisse
Strukturierte und selbständige Arbeitsweise mit hoher Eigenverantwortung
Teamorientiertes Denken, klare Kommunikation und hohe Belastbarkeit
Offen für neue Technologien und agile Arbeitsweisen
Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus. Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar. Wie wir unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst. Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt. Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.
Menschen werden Teil der Lonza, um herausfordernde und komplexe Problemstellungen durch kreative und innovative Ansätze im Bereich Life Sciences zu lösen. Im Gegenzug bieten wir die Zufriedenheit, die mit der Verbesserung des Lebens auf der ganzen Welt einhergeht. Die Zufriedenheit, die damit einhergeht, einen sinnvollen Unterschied zu machen.
Bereit, die Zukunft der Life Sciences mitzugestalten? Dann bewirb dich jetzt!
weniger ansehen