301 Jobs in Dallenwil
Regulatory Affairs Expert
Oberdorf, Nidwalden
Fresenius Medical Care North America
Gestern
Job angesehen
Arbeitsbeschreibung
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
+ **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
Leider ist dieser Job in Ihrer Region nicht verfügbar
0
Quality Systems Analyst II (fix term until December 2026)
Oberdorf, Nidwalden
J&J Family of Companies
Vor 11 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Quality
**Job Sub** **Function:**
Quality Systems
**Job Category:**
Professional
**All Job Posting Locations:**
Oberdorf, Basel-Country, Switzerland
**Job Description:**
**About MedTech**
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at are searching for the best talent for a Quality Systems Analyst II located in Oberdorf (Basel Land), Switzerland.**
_This is a fixed term contract that will run until December 2026._
The Oberdorf Quality Systems Team is responsible for the compliance and continuous improvement of the site's Quality System (QS). In this role, you will work in a collaborative environment with various stakeholders and get hands-on experience with internal and external audits. The Quality Systems Analyst II will drive the execution of the QS at the site level, including Nonconformances (NC), Corrective and Preventive Action (CAPA), Internal Audit (IA) Observations, Product Quality Escalation, Site Complaint Manufacturing Investigations, Quality Progress Review (QPR), Quality System Management Review (QSMR), and Records Management to ensure the QS meets all business and regulatory requirements. You will also manage the performance and communication of Oberdorf QS metrics, as well as support site readiness in the deployment of QS initiatives.
**As a Quality Systems Analyst, you will:**
+ Ensure consistent and correct execution of QS procedures at the site to maintain the quality and compliance of processes and records for NC, CAPA, IA Observations. This includes, but is not limited to:
+ Review site CAPAs, NCs, IA Observations, Site Complaint Manufacturing Investigations, QPR and QSMR documentation
+ Assist with the development and documentation of problem statements, bounding, containment, risk assessments, investigation, and action plan determination (corrections, corrective actions, preventive actions, and effectiveness monitoring)
+ Ensure effective completion of activities
+ Provide guidance to record owners for appropriate documentation and compliant execution of procedures
+ Coordination, preparation, facilitation, execution, and tracking of activities of the Quality Progress Review (QPR) and Quality System Management Review (QSMR).
+ Have oversight and support the tracking of QS metrics at site level. Communicate status and issues to stakeholders and management, as needed.
+ Support site Records Information Management activities.
+ Provide guidance on requirements and develop the competency of resources that execute the aforementioned QS processes.
**Qualifications**
+ University/Bachelor's Degree or Equivalent preferred (e.g., Technical Qualification with Further Education)
+ Two (2) years related experience in Medical Device or Pharmaceutical environment, or equivalent combination of education and experience
+ Experience in technical writing, such as root cause investigations of NCs, CAPAs, and Observations
+ Awareness of ISO standards and Quality System regulations
+ Advanced use of computer and software applications (e.g. Microsoft PowerPoint, Word, Excel, SharePoint, and Teams)
+ Soft Skills
+ Detail-oriented and high level of accuracy
+ Pro-active approach to execution of deliverables and managing stakeholders
+ Time-oriented (i.e. able to recognize and adhere to strict timelines)
+ Strong communication and interpersonal skills (collaboration with multiple stakeholders is required)
+ Ability to follow-up with management-level stakeholders, and challenge, as necessary to ensure compliance to procedural requirements
+ Strong English-proficiency is required for the role (successful candidate must be able to facilitate meetings and write documentation in English)
**Preferred:**
+ German-proficiency is advantageous
+ Experience facilitating or supporting Management Reviews or Quality Metric Reviews
+ Experience in working in a manufacturing/operations environment
+ Experience in Quality Systems process development and improvement
+ Experience in Quality and notified body inspections
At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.
**Here's** **what you can expect:**
+ **Application review:** We'll carefully review your CV to see how your skills and experience align with the role.
+ **Getting to know you:** If there's a good match, you'll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
+ **Staying informed:** We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
+ **Final steps:** For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide youthrough these.
Finally, at the end of the process, we'll invite you to share feedback in a short survey - your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We're excited to learn more about you and wish you the best of luck in the process! #RPOEMEA
Quality
**Job Sub** **Function:**
Quality Systems
**Job Category:**
Professional
**All Job Posting Locations:**
Oberdorf, Basel-Country, Switzerland
**Job Description:**
**About MedTech**
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at are searching for the best talent for a Quality Systems Analyst II located in Oberdorf (Basel Land), Switzerland.**
_This is a fixed term contract that will run until December 2026._
The Oberdorf Quality Systems Team is responsible for the compliance and continuous improvement of the site's Quality System (QS). In this role, you will work in a collaborative environment with various stakeholders and get hands-on experience with internal and external audits. The Quality Systems Analyst II will drive the execution of the QS at the site level, including Nonconformances (NC), Corrective and Preventive Action (CAPA), Internal Audit (IA) Observations, Product Quality Escalation, Site Complaint Manufacturing Investigations, Quality Progress Review (QPR), Quality System Management Review (QSMR), and Records Management to ensure the QS meets all business and regulatory requirements. You will also manage the performance and communication of Oberdorf QS metrics, as well as support site readiness in the deployment of QS initiatives.
**As a Quality Systems Analyst, you will:**
+ Ensure consistent and correct execution of QS procedures at the site to maintain the quality and compliance of processes and records for NC, CAPA, IA Observations. This includes, but is not limited to:
+ Review site CAPAs, NCs, IA Observations, Site Complaint Manufacturing Investigations, QPR and QSMR documentation
+ Assist with the development and documentation of problem statements, bounding, containment, risk assessments, investigation, and action plan determination (corrections, corrective actions, preventive actions, and effectiveness monitoring)
+ Ensure effective completion of activities
+ Provide guidance to record owners for appropriate documentation and compliant execution of procedures
+ Coordination, preparation, facilitation, execution, and tracking of activities of the Quality Progress Review (QPR) and Quality System Management Review (QSMR).
+ Have oversight and support the tracking of QS metrics at site level. Communicate status and issues to stakeholders and management, as needed.
+ Support site Records Information Management activities.
+ Provide guidance on requirements and develop the competency of resources that execute the aforementioned QS processes.
**Qualifications**
+ University/Bachelor's Degree or Equivalent preferred (e.g., Technical Qualification with Further Education)
+ Two (2) years related experience in Medical Device or Pharmaceutical environment, or equivalent combination of education and experience
+ Experience in technical writing, such as root cause investigations of NCs, CAPAs, and Observations
+ Awareness of ISO standards and Quality System regulations
+ Advanced use of computer and software applications (e.g. Microsoft PowerPoint, Word, Excel, SharePoint, and Teams)
+ Soft Skills
+ Detail-oriented and high level of accuracy
+ Pro-active approach to execution of deliverables and managing stakeholders
+ Time-oriented (i.e. able to recognize and adhere to strict timelines)
+ Strong communication and interpersonal skills (collaboration with multiple stakeholders is required)
+ Ability to follow-up with management-level stakeholders, and challenge, as necessary to ensure compliance to procedural requirements
+ Strong English-proficiency is required for the role (successful candidate must be able to facilitate meetings and write documentation in English)
**Preferred:**
+ German-proficiency is advantageous
+ Experience facilitating or supporting Management Reviews or Quality Metric Reviews
+ Experience in working in a manufacturing/operations environment
+ Experience in Quality Systems process development and improvement
+ Experience in Quality and notified body inspections
At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.
**Here's** **what you can expect:**
+ **Application review:** We'll carefully review your CV to see how your skills and experience align with the role.
+ **Getting to know you:** If there's a good match, you'll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
+ **Staying informed:** We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
+ **Final steps:** For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide youthrough these.
Finally, at the end of the process, we'll invite you to share feedback in a short survey - your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We're excited to learn more about you and wish you the best of luck in the process! #RPOEMEA
Leider ist dieser Job in Ihrer Region nicht verfügbar
1
Carrosserielackierer 60-100%
Stans, Nidwalden
Manpower
Vor 5 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Manpower
Das gemeinsame Ziel, mit Begeisterung an der Arbeit, verbindet. Bei unserem Kunden kommen rund 85 Mitarbeitende aus elf Nationen und mit einem breiten Altersspektrum von Anfang 20 bis zum Pensionsalter zusammen. Die Zusammenarbeit funktioniert auf Augenhöhe ? geprägt von gegenseitigem Respekt und Vertrauen.
-Prüfen und Bewerten sowie Vorbereiten von Untergründen
-Vorbereiten von Fahrzeugen für Lackierarbeiten
-Lackieren von einzelnen Bauteilen, Ganzen Fahrzeugen (Neuwagen, Gebrauchtwagen Nutzfahrzeuge, Oldtimer etc.)
-Ausführen von einfachen Demontage- und Montagearbeiten
-Bereitstellen und Mischen von Farben nach technischen Vorschriften
-Herstellen von Design- und Effektlackierungen
-Finish-Arbeiten und Ausführung der Lackpflege
-Abgeschlossene Ausbildung als Carrosserielackierer oder vergleichbare Qualifikation
-Berufserfahrung in der Fahrzeuglackierung
-Kenntnisse im Umgang mit Lackierwerkzeugen und -maschinen
-Teamfähigkeit und Zuverlässigkeit
-Führerschein der Klasse B von Vorteil
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: Automobilindustrie
Funktion: Produktion
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2
Industrielackierer 60-100%
Stans, Nidwalden
Manpower
Vor 5 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Manpower
Das gemeinsame Ziel, mit Begeisterung an der Arbeit, verbindet. Bei unserem Kunden kommen rund 85 Mitarbeitende aus elf Nationen und mit einem breiten Altersspektrum von Anfang 20 bis zum Pensionsalter zusammen. Die Zusammenarbeit funktioniert auf Augenhöhe ? geprägt von gegenseitigem Respekt und Vertrauen.
-Nasslackieren von Aluminium-, Kunststoff und Holzteile für Bahn- und Luftfahrtindustrie
-Schleif-, Abdeckungs- und Finisharbeiten
-Pflege der nötigen Werkzeuge und Anlagen
-Bereitstellen und Mischen von Farben nach technischen Vorschriften
-Abgeschlossene Ausbildung als Industrielackierer oder vergleichbare Qualifikation
-Berufserfahrung in der industriellen Lackierung
-Kenntnisse im Umgang mit Lacken, Farben und Lackiertechniken
-Sorgfältige und präzise Arbeitsweise
-Teamfähigkeit und Belastbarkeit
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: Produktion
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3
Rohrleitungsmonteur Gas- und Fernwärmenetze (PE / Guss / Versorgungstechnik)
Stans, Nidwalden
DAS PERSONAL.
Vor 2 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Aufgaben
- Montage und Instandhaltung von Gas-, Wasser- und Fernwärmeleitungen (PE- und Gussleitungen)
- Durchführung von Wasser- und Erdgasproben
- Reparatur- und Unterhaltsarbeiten an Versorgungsnetzen
Qualifikation
- Abgeschlossene Ausbildung als Sanitärinstallateur, Heizungsinstallateur, Schlosser oder vergleichbare Berufslehre – oder mehrjährige Erfahrung im Leitungs- bzw. Rohrleitungsbau
- Freude an präzisem Handwerk und Teamarbeit
- Führerschein Kat. B von Vorteil
Benefits
- Attraktiver Lohn (Vergütung)
- Bonuszahlungen bei erfolgreicher Vermittlung von neuen Mitarbeitern
- Karriere- und Weiterbildungschancen
- Persönliche Betreuung
Wir freuen uns auf Ihre Bewerbung!
Branche: Bauwesen/Bauingenieurwesen
Funktion: Bauwesen/Handwerk
Anstellungsart: Festanstellung
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4
Anlagen- und Apparatebauer EFZ Umgebung Nidwalden
Stans, Nidwalden
DAS PERSONAL.
Vor 23 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Aufgaben
- Verlegen & Montieren von Rohrleitungen
- Schweiss- & Verbindungstechniken anwenden
- Arbeiten nach Plan und in Teamkoordination
- Funktionsprüfungen & Instandhaltung
Qualifikation
- Erfahrung im Rohrleitungsbau, Anlagenbau oder als Rohrschlosser
- Kenntnisse in Schweissverfahren & technischen Zeichnungen
- Selbständiges Arbeiten & Teamspirit
Benefits
- Attraktiver Lohn (Vergütung)
- Bonuszahlungen bei erfolgreicher Vermittlung von neuen Mitarbeitern
- Karriere- und Weiterbildungschancen
- Persönliche Betreuung
Wir freuen uns auf Ihre Bewerbung!
Branche: Bauwesen/Bauingenieurwesen
Funktion: Bauwesen/Handwerk
Anstellungsart: Try and Hire
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5
Werkstattmonteur 100% (m/w/d) - die Wasserkraft funktioniert nur, weil Profis in Werkstätten dafü...
Kriens, Luzern
PKS Personal AG
Vor 12 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
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.
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6
Development Engineer (contract)
Rotkreuz, Zug
Roche
Heute
Job angesehen
Arbeitsbeschreibung
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.**
**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.**
Leider ist dieser Job in Ihrer Region nicht verfügbar
7
Senior Software Engineer (80-100%)
Rotkreuz, Zug
Roche
Gestern
Job angesehen
Arbeitsbeschreibung
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.**
**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.**
Leider ist dieser Job in Ihrer Region nicht verfügbar
8
Management Partner
Rotkreuz, Zug
Roche
Vor 2 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
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.**
**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.**
Leider ist dieser Job in Ihrer Region nicht verfügbar
9