238 Jobs in Hellbühl

Manpower

MANPOWER AG ist spezialisiert auf Temporär- und Dauerstellen und bietet umfassende Personaldienstleistungen an. Mit Standorten in der ganzen Schweiz unterstützen wir unsere Kunden, um deren Aufträge und Projekte erfolgreich zu realisieren. Für unseren Kunden in der Region suchen wir

Produktionsplaner 80-100% (m/w/d)

Ihre Aufgaben:

• Drehscheibe zwischen Produktion, Verkaufsinnendienst, Materialwirtschaft und weiteren betriebsinternen Stellen
• Bearbeiten von Produktionskennzahlen zur Indenifikation von Schwachstellen und Optimierung der Planung
• Optimales Einplanen unserer Gebäckspezialitäten zur effizienten Nutzung der Personal- und Anlageressourcen
• eine maximale Lieferbereitschaft sicherstellen der zugeteilten Produktionsanlagen

Ihr Anforderungsprofil:

• Technische Grundausbildung (EFZ) und Berufserfahrung in der Produktionsplanung oder in der Lebensmittelindustrie
• Betriebswirtschaftliche Weiterbildung (z.B. Prozessfachmann/-frau, technischer Kaufmann / Kauffrau von Vorteil)
• Erfahrung im Umgang mit ERP-Systemen (CSB, SAP, o.ä.)
• Kundenorientierte Persönlichkeit mit strukturierter Arbeitsweise und vernetztem Denken

Interessiert? Dann bewerben Sie sich noch heute über den Online Button ? gerne auch ohne Motivationsschreiben.
Für weitere Auskünfte über diese Stelle erreichen Sie uns unter Telefon

Branche: Nahrungsmittelproduktion

Funktion: Facility Management/Maintenance Service/Reinigung

With our international recruitment services, we support hospitals, nursing homes, medical practices, rehabilitation clinics, and physiotherapy practices in their search for qualified employees. For our clients in the health care sector in Switzerland, we are looking for physiotherapists (m/f/d) for permanent positions. 

During the entire application process, we will accompany you personally in Germany together with our local partner in Switzerland and introduce you to medical institutions. If you are in search for a new opportunity to bring out your experience and potential, we would like to meet you immediately.

Locations: Feel free to mention the location / canton you wish to work on the application form.

Tasks:

Carrying out physiotherapeutic treatment.Professional and independent work.Keeping documentation, reports and assesments. Carrying out home visits and visits to care centres if necessary. Requirements

Your Profile:

Successfully completed physiotherapy training.Team player, friendly presentation.Professional and independent work.Excellent patient care and communication skills.Ideally, you have completed training in the field of manual therapy, but this is not a prerequisite. Info for international applicants:  Proficiency (min.B2) in at least one national language such as German, French or Italian. German skill is a plus  Recognition of foreign professional qualification.

We look forward to receiving your application with:

- CV (photo optional, but welcome).

- Letter of motivation 

- Diploma / Certificates

- References / Recommendations.

BenefitsHigh professional appreciation.Above-average salary in comparison with the EU.Good working conditions& more.

Montageprofis für eine energiegeladene Zukunft 

Für unseren Kunden, ein Anbieter im zukunftsträchtigen Markt des Umbaus und der Modernisierung von Wasserkraftwerksanlagen suchen wir aktuell eine versierte, selbständige und teamfähige Persönlichkeit als

Ihre Aufgaben:

• Ausführen von De- und Remontagearbeiten an Systemen und / oder Komponenten von Wasserkraftanlagen
• Durchführung von Druckproben, Funktions- und Qualitätskontrollen
• Bereitstellen der Komponenten für die Spedition
• Durchführung von Ein- und Ausgangskontrollen an den Komponenten
• Ausführen verschiedener Logistikarbeiten
• Mithilfe bei der Durchführung von Bestandesaufnahmen
• Gelegentliche Montageeinsätze beim Kunden vor Ort

Ihr Profil:

• Grundausbildung in einem technischen Beruf (Polymechaniker Fachrichtung Montagetechnik, Landmaschinen- oder LKW-Mechaniker)
• Spezifische Fachkenntnisse in der Montagetechnik, vorzugsweise im Bereich Wasserkraftanlagen
• Mindestens 3 Jahre Erfahrung in der Montagetechnik
• Anwenderkenntnisse in MS-Office zwingend, SAP von Vorteil
• Gute Deutschkentnisse (mindestens B2)
• Staplerprüfung, Kranführer Ausweis

 

Unser Angebot:

• Flexible Arbeitszeiten (Jahresarbeitszeit)
• Fortschrittliche Anstellungsbedingungen (GAV Swissmem)
• Selbstständige, vielseitige Tätigkeiten im Umfeld der erneuerbaren Energien
• Zentraler Arbeitsort mit hervorragender, umliegender Infrastruktur
• Offene, informelle Unternehmenskultur

Ich stehe Ihnen für weitere Informationen gerne zur Verfügung. Ich freue mich auf Ihre vollständige Bewerbung. Diskretion zugesichert.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
In a global, cross-functional environment, the System Development (SD) department is responsible for workflow optimization and successfully integrating hardware, software, consumables, and reagents to perform the system verification of diagnostics instruments.
As a Development Engineer, you will work as a part of a cross-functional team, working on Nucleic Acid Purification, PCR and Sequencing, on developing complex diagnostics systems. You will perform hands-on experiments, Hardware (HW) and Software (SW) testing, including evaluation of system performance, error handling, and reliability improvements.
**_Please note that this vacancy is not currently linked to an open position. We are anticipating future needs in our organization. If you are interested in this kind of role, please apply today, and we may contact you should a position matching your profile become available._**
In this position, you will be responsible for the following areas:
+ Plan and execute the work packages within the area of responsibility, including reporting and escalating issues to management.
+ Subject matter expert for an assigned area of responsibility. Provide guidance and support to team members.
+ Generate required documentation/procedures/technical reports.
+ Prepare and deliver presentations of project results to team and management.
+ Experimental design and execution of the experiments in the biosafety levels S1 and S2 laboratory.
+ Creation of Test Cases based on Product Requirements. Execution of Test Cases, analysis of the results, and creation of the respective regulatory documents. Issue tracking and verification of bug fixes/Anomalies.
+ Troubleshoot, debug, and upgrade existing systems. Document and maintain software functionality.
+ Coordinate efforts with other functional areas to accomplish tasks: Hardware, Software-, Consumables-and Assay-Development.
Who you are
You are someone who wants to influence your development. You are looking for a company where you have the opportunity to pursue your interests across functions and geographies. A job title is not considered the final definition of who you are but the starting point.
The ideal candidate for our dynamic, international team will have the following skills and experience:
+ Degree in a relevant life science discipline (e.g. (e.g. biology, biotechnology, biomedical informatics, engineering related to life sciences) or corresponding job experience
+ Interest in resolving technical problems and interdisciplinary teamwork
+ Experience and willingness to work in a highly regulated industry and labs with biosafety levels S1 and S2.
+ Familiarity with or strong interest in software and engineering applications and tools .
+ Enthusiastic team player with good communication and collaboration skills. Solution-oriented, autonomous, and proactive working style.
+ Proven experience in laboratory diagnostics and/or service & support, as well as supporting HW and SW, are additional assets.
+ Working knowledge of English (written and spoken), and German a strong asset
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
A healthcare pioneer and the industry's global leader in in-vitro diagnostics, the Diagnostics Division pushes boundaries and challenges the status quo to redefine what's possible. Our commitment to research and development means we can bring to the market integrated solutions in diagnostic testing, laboratory efficiency, healthcare digitalization and decision support tools and software. Our products deliver increasingly precise information to help save lives, prevent or control the risk of infection and monitor treatment effectiveness.
RDS R&D is structured in four networks (Core Lab Development, Pathology Lab Development, Point of Care Development, Molecular Lab (PCR Development and Sequencing R&D) and four chapter areas (Computational Science & Informatics (CSI), Diagnostics Standards & Interoperability (DSI), Reagent Research & Design (RRD) and Research & Early Development (RED). The international teams are located on various sites and countries across the globe.
We are looking for a full stack **Senior Software Engineer** to strengthen our Legacy & Biotech ART. In this challenging position, you will be a key member of our product care organization, drive innovation and create added value for our customers in the area of healthcare core labs and for our biotech customers. This is a hands-on software development position where you define, build, test and release high-quality software for IVD and non-IVD products. As a domain expert, you will have a large influence on projects to enhance our future product portfolio.
**The Opportunity:**
+ You perform and take ownership of specific software development tasks, ensuring reviews using checklists and templates.
+ You lead work package definition, estimation, and planning, and enhance or document SW unit specifications and designs.
+ You review designs and contribute to the SW architecture, defining quality attributes and staying updated with technology trends.
+ You conduct root-cause analysis of complex issues and provide bug fixes for post-market software releases.
+ You ensure compliance with processes, propose improvements, and stay informed about regulatory and market standards.
**Who you are:**
You're a self motivated team player, who wants to influence your own development. It is natural for you to be proactive in working with your teammates and in working with other parts of the organization. You like sharing your Know-how to help the whole team advance. Bringing in new ideas to improve existing products with new functions and cost optimization is important to you. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.
Must Haves:
+ Educational Background: Bachelor's degree in a software engineering-related field.
+ Professional experience in software engineering, preferably in a regulated environment or medical device industry.
+ Technical Skills: Proficient in C++ and at least one other object-oriented language; knowledge of git.
+ Language Skills: Fluent in English, Basic knowledge of German (Level A2)
+ Team Collaboration: Strong team player committed to writing good documentation.
Nice-to-Haves:
+ Experience in agile environments, ideally with SAFe
+ Knowledge of Linux incl. Shellscripting, Microsoft Windows SDK/MFC, Containers(Podman), QT, Powerbuilder
+ Experience with Oracle or any other relational Database System
**Ready to take the next step? We'd love to hear from you. Apply now to explore this exciting opportunity!**
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**

At Fresenius Medical Care, we're dedicated to improving the lives of patients with chronic kidney disease through innovative, high-quality products and treatments. Our vision- **"** **Creating a future worth living. For patients. Worldwide. Every day.** "-guides everything we do. With over 125,000 people working across 3,700 dialysis centers and 39 manufacturing sites worldwide, we provide direct patient care through our Care Delivery network, develop and supply medical products, therapies, digital solutions via Care Enablement, and accelerate transformation through our FME Reignite strategy. Our values drive us:
+ **We Care** for our patients, each other, and our communities.
+ **We Connect** across teams and borders to deliver excellence together.
+ And **we Commit** to doing things the right way, growing with purpose, and leading kidney care with innovation and compassion.
As part of this commitment, Systems, Quality & Regulatory (SQR) **-** a global function within Care Enablement-ensures product quality and safety, regulatory compliance, and market access throughout the entire product lifecycle. The team drives quality across manufacturing and supply chain processes, manages post-market surveillance, and promotes continuous improvement, system harmonization, and sustainability. SQR also oversees Q&R data governance and delivers key product-related business services. Join our passionate team and help shape healthcare worldwide!
As a Title, your role will focus on on Drug Safety as PvRP (Pharmacovigilance), Local Drug Regulatory Affairs and Good Distribution practice (FVP/RP) in Switzerland and Austria.
**RESPONSIBILITIES** :
LDRA:
+ Executes RA activities in line with defined procedures and processes.
+ Obtain product registration dossiers from HQ Q&R and tailor them to meet country/region registration
+ requirements
+ Implement processes involved with maintaining annual licenses, registrations, and listings
+ Submit notifiable changes and supplemental dossiers to the appropriate regulatory authorities to update product
+ information and/or instructions for use to reflect current state of product knowledge
+ Support and accelerate market access for our products in line with regulatory requirements, verticals and
+ commercial operations roadmap. Contribute to the Due diligences for in-licensing projects and to the preparation
+ of the launch for new development project for all regulatory aspects.
+ Serve as the Regulatory point of contact on the assigned task(s) with local/regional management and/or at other
+ internal meetings providing the agreed global regulatory strategic recommendations and risk assessment for key
+ projects.
+ Monitor, evaluate and inform key internal stakeholders about applicable national and hub regulatory
+ requirements; coordinate internal implementation and actively contribute to the development of new regulatory
+ requirements.
+ Perform all regulatory affairs activities in the hub including management of product complaints and product
+ regulatory conformity, safety, and post market systems as well as communication to applicable SysQaRa
+ functions in accordance with corporate SOPs
+ Perform based on established targets, KPIs and objectives for Q&R.
PVRP:
+ Perform regular Pharmacovigilance processes and activities (including trainings).
+ Ensure that adverse events and product quality complaints are reported in compliance with corporate policies
+ and procedures.
+ Lead the strategic planning and implementation of pharmacovigilance objectives in your country/region, including
+ department structure, processes, and local Health Authority policy implementation.
+ Maintain the filing, storage, and archiving of safety-related documentation in accordance with company policies
+ and local requirements.
+ Ensure audit / inspection readiness, coordinates, leads, and actively participates in local audits and inspections.
+ Support Pharmacovigilance Agreements, when applicable.
FVP/GDP RP:
+ Ensure that a Quality management system is implemented and maintained,
+ Focus on the management of authorized activities (GDP) and the accuracy and quality of records.
+ Ensure that initial and continuous training programs are implemented and maintained,
+ Coordinate and promptly perform any recall operations for medicinal products,
+ Ensure that relevant customer complaints are dealt with effectively,
+ Ensure that suppliers and customers are approved,
+ Approve any subcontracted activities which may impact on GDP
+ Keep appropriate records of any delegated duties,
+ Decide on the final disposition of returned, rejected, recalled or falsified products,
+ Approve any returns to saleable stock
+ Ensure that any additional requirements imposed on certain products by national law are adhered to
**REQUIREMENTS:**
+ Scientific education such as Degree in Medicine, Pharmacy, Biology, Chemistry and/or related Engineering degree(s).
+ Desirable 5 years professional experience in regulatory management of medicinal products respectively similar activity in the regulated
+ environment.
+ Communicative, reliable, careful, conscientious, quality minded, detail oriented
+ Regulatory and PV guidelines (EU, local)
+ Switzerland: Therapeutic Products Act (TPA) Act, TPA)(Therapeutic Products Act, TPA)(Therapeutic Products Act, TPA)
+ Austria: Medicinal Products Act (AMG)
+ MDR/MDD
+ GDP
+ Microsoft Office, related MS applications
+ Knowledge of German and English languague both in word and writing
+ Good regulatory understanding
+ Good communication skills
**Our Offer for you:**
There is a lot you can discover at Fresenius Medical Care, regardless in which field you are an expert and how much experience you have - all dedicated to your professional journey.
+ Whether in front of or behind the scenes - you are helping to make ever better medicine available to more and more people around the world
+ Individual opportunities for self-determined career planning and professional development
+ A corporate culture in which there is enough room for innovative thinking - to find the best solution together, not the quickest one
+ A large number of committed people with a wide range of skills, talents and experience
+ The benefits of a successful global corporation with the collegial culture of a medium-sized company

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
As the Management Partner Automation, you will be the personal assistant for the Lifecycle Leaders Automation and the Program Lead cobas ultra.
**The opportunity**
+ Administrative business support: **calendar management,** **email management** , general tasks such as **PO and invoice management**
+ **Coordination of meetings** and **events** : organize internal and external meetings including room reservations, agenda, catering, budget, etc.
+ **Travel and expenses** : flight, hotel, car rental, transfer bookings; visa organization; interface to hotels, business partners, others; expense management; etc.
+ Other tasks such as IT equipment, **access management,** support for **onboarding of new employees**
**Who you are**
+ Highly organized and adaptable, with excellent **time management** skills
+ Strong interpersonal abilities and clear, **professional communication style**
+ Collaborative **team player** with a proactive attitude
+ Fluent in both English and German
+ Educational background: completed apprenticeship in a **business-related field** or a bachelor's degree / higher education diploma as a **management assistant,** with initial hands-on **experience** in a similar role
+ Willing and able to work on site **at least 80%** of the time
**Application documents - a pragmatic approach:**
We kindly ask you to provide a brief explanation of what interests you about this position, a current CV, and your official educational certificates/proof of qualifications. No additional documents are required at this stage.
Please note that no further documents can be added after the application has been submitted.
Apply now - we look forward to hearing from you!
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
Shape the future of Core Lab innovation. Lead a team where technical excellence meets collaborative spirit.
Are you passionate about leading experts who define and design new complex diagnostic systems? As Team Lead Solution & System Definition, you'll drive innovation, nurture talent, and set the strategic direction for our Core Lab systems and solutions - all while fostering a culture of excellence, growth, and collaboration.
**The Opportunity**
In this leadership role, you will guide a dedicated team of specialists responsible for defining and architecting cutting-edge Core Lab solutions. You'll combine strategic vision with operational excellence, ensuring regulatory compliance, quality, and innovation across projects.
+ You lead and develop a medium-sized team of experts in system design, architecture, requirements and risk management
+ You foster a culture of innovation, learning, and continuous improvement through coaching and feedback
+ You define system concepts, requirements, and specifications for Core Lab solutions
+ You ensure compliance with quality and regulatory standards (TÜV, FDA, NMPA)
+ You manage team performance, goals, and resource allocation effectively
+ You translate strategic direction into actionable tasks and competencies
+ You drive collaboration across R&D networks and interdisciplinary teams
+ You champion change initiatives and promote a positive, solution-oriented mindset
+ You oversee risk-based management and documentation quality
+ You support onboarding and building capability for new team members
**Who You Are**
You are a strategic and people-oriented leader who thrives on complexity and collaboration. You combine technical depth with an ability to inspire and empower others.
+ You have a Degree (Bachelor, Master, or PhD) in natural sciences, (system) engineering, or related field
+ You have several years of experience in the diagnostics or related highly regulated industry
+ You have proven leadership skills with a strong coaching mindset
+ You have deep knowledge of IVD development, system architecture, and risk management
+ You have experience with regulatory standards and quality documentation
+ You have strong stakeholder management and communication skills
+ You are fluent in English; German is a plus
+ You have excellent collaborator in cross-functional, international settings
Are you ready to apply? We want someone who thinks beyond the job offered - someone who knows that this position can be a unique opportunity to shape the future of Roche.
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**

**Design Your Future at PVH**
Stock Coordinator in Teilzeit Luzern Tommy Hilfiger (m/w/d)
PVH ist eines der erfolgreichsten Mode- und Lifestyle-Unternehmen der Welt. Unser Markenportfolio umfasst die iconic brands CALVIN KLEIN und TOMMY HILFIGER. Mit mehr als 30.000 Mitarbeiter:innen, die in über 40 Ländern tätig sind, steht PVH wie kein anderes Unternehmen mit der fortschreitenden Digitalisierung und Integration aller Kanäle für Weiterentwicklung und Innovation.
Eine der größten Stärken von PVH sind unsere Mitarbeiter:innen und unser gemeinsamer Wunsch, ein integratives Arbeitsumfeld zu schaffen, in dem jede(r) Einzelne geschätzt und jede Stimme gehört wird. Gemeinsam setzen wir uns für eine vielfältigere und gerechtere Modebranche ein, um nachhaltige Veränderungen sowohl bei PVH als auch in unserer Branche voranzutreiben.
Für unseren Store in Luzern suchen wir eine(n) **Stock Coordinator (m/w/d)** .
Mit deiner Hands-On Mentalität und deinem Organisationstalent bist du für das Lagermanagement unseres Stores verantwortlich. Die gute Zusammenarbeit zwischen Lager und unserer Verkaufsfläche wird durch deinen Teamgeist und deine Dynamik geprägt und deine Proaktivität hilft dir, Lösungen für mögliche Herausforderungen zu finden.
**Deine Aufgaben:**
+ Die Sicherstellung und Überblick aller Lager-Aufgaben
+ Die Warenannahme und -sicherung
+ Die Kontrolle der Lieferscheine
+ Die Bestandspflege und -kontrolle
+ Die Kommissionierung von Warentransfers
+ Der Austausch mit Fachabteilungen wie Retail Operations und Merchandise Allocation
+ Der Umgang mit unseren Omni-Channel Systemen
**Was brauchen wir von dir?**
+ Eine erfolgreich abgeschlossene Ausbildung zur Fachkraft für Lagerlogistik oder eine ähnliche kaufmännische Ausbildung
+ Idealerweise Berufserfahrung im Lagerumfeld
+ Teamfähigkeit und eine Hands-On Mentalität
+ Flexibilität, Belastbarkeit und Organisationstalent
+ Gute Englisch- und PC-Kenntnisse (MS Office)
**Was du von uns erwarten kannst:**
+ Eine attraktive Vergütung inklusive Bonussystem, 13. Monatsgehalt sowie fünf Wochen Urlaub im Jahr
+ Spannende interne Aufstiegs- und Weiterbildungsmöglichkeiten
+ Vielfältige Mitarbeitervorteile, wie Mitarbeiterrabatte, Staff Outfits und andere Initiativen
+ Zahlreiche Angebote für deine mentale Gesundheit
+ Lead Yourself. Lead Together. Lead the Way. Bei PVH ist jede(r) eine Führungskraft - egal, ob du ein Team oder ein Projekt leitest oder einfach dein Expert:innenwissen einbringst. Unsere PVH Leadership Behaviors stellen sicher, dass wir das Potenzial eines/einer jeden von uns freisetzen
+ Die Möglichkeit, eigenverantwortlich zu arbeiten sowie Prozesse mitzugestalten und zu optimieren
+ Ein lifestyleorientiertes Arbeitsumfeld in einem dynamischen, umweltbewussten, wachsenden Unternehmen
Unsere Mitarbeiter:innen kommen aus allen Lebensbereichen und Ecken der Welt zusammen. Inklusion und Diversität sind wesentliche Pfeiler in unserer Unternehmenskultur. Wir wissen, dass uns Vielfalt stärker macht. Unabhängig von Herkunft, Nationalität, Glaube, Behinderung, Alter, Familienstand, Partnerschaftsstatus, sexueller Orientierung und Geschlecht bist du bei uns willkommen.
DIVERSITY & EQUAL OPPORTUNITY We are committed to recruiting, training and providing career advancement to all associates regardless of gender, race, religion, age, disability, sexual orientation, nationality, or social or ethnic origin. Diversity in the workplace is encouraged. Bigotry, racism and any form of harassment or discrimination is not tolerated.