Gehaltsübersicht für Manufacturing Engineer in Schweiz

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Widespread IT technical knowledge such as Operating System, Infrastructure and Networking. Programming is excluded and development of script is very limited. Proficiency into Computer System Validation in the pharmaceutical environment is required. The accountability of the worker is the improvement or full implementation of off-the-shelf and configurable (Gamp3 and 4) standalone and interconnected standalones, regulated by the GmPs. To a lesser extent, he will collaborate on (Gamp5) worldwide/interconnected systems. Skills/Knowledge Required Pharmaceutical, Biotechnology, Life Science industry experience is a must. 3-5 years’ experience as an IT Engineer running project from requirements to delivery of final product and documentation included. Familiar with Change Management tools and regulated document authoring. COTS and Web-based requirements, architecture, Agile/SCRUM methodology. Real Time Data Management and Interfaces (e.g.: Kepware, OSI PI) a strong plus Serialization technologies (Laetus) a strong plus Six Sigma, Lean or Business Process Change Techniques a plus Technical diploma in Information Systems or equivalent experience Experience in Computer System Validation Awareness of 21-CFR Part 11, Eudralex, MHRA Awareness of business and enterprise architecture Fully operational in French and English Business acumen Autonomous in analysis, problem solving and achieving deliverables Oral and Written communication Constructive influencing of colleagues to positive outcome Duties and Responsibilities Information Technology Requirements, GmP Regulation, must be explained and obtained from the vendor of system. When necessary, the Engineer, may have to customize the system, or adapt the process, to comply the GmPs. Guarantee Data Integrity of the system into its environment and process. Design through elicits, analyzes, documents, and validates detailed user / functional / non-functional requirements; identify gaps between system capabilities and requirements to ensure that business needs are met. Adjust the number of deliverables, their quality and complexity to guarantee the respect of timelines and fit to validation approach. Facilitate meetings with business colleagues on IT topics Assist the translation of compliance requirements into test conditions and expected results for application functionality, and acceptance testing (IQ, OQ, PQ, FAT, SAT) Understand business objectives, processes, and strategies. Drive development and execution of change management and training throughout the organization during the implementation and ongoing use of system applications Ability to work strategically and independently with internal and external groups on multiple simultaneous projects Understand and ensure the use of existing standards for design and governance. Architect system specific topology and adapt/integrate it into existing infrastructure. Collaborate with IT groups to ensure standards are applied for technological tools. Use existing standard to capitalize on lessons learned. Define new versatile solutions covering abstract User Requirements to fulfill unmet needs. Implement specific standalone and interconnected computerized system supporting activities like Production (e.g.: Laetus Track & Trace, Blending, Encapsulation, Tablet Press, Blistering, Bottling, Cartoning, Room Monitoring System and other various equipment used for the manufacturing, packaging and Quality Control of drug products. Usage of a wide variety of Information Technology skills to configure systems, implement backup mechanism for flat files, databases, etc. Deploy proper privileges on Operating System (Windows) and File Systems. Develop governance and “how to” Work Practices, including their Configuration Specifications to allow the operational team to support and administer the newly integrated system. Transmit information and follow up with specialists to obtain required configuration of the global network, backup tool and infrastructure. Configure and setup local network, infrastructure, computers and applications. Preparation and configuration of interfaces between multiple system may be required. Usage of Kepware technology and OPC protocol will be required. If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:1112 Celgene International SaRL

JOB DESCRIPTION: Thoratec Switzerland GmbH is part of the medical device division of Abbott Laboratories, a fortune 500 company with over 115’000 employees worldwide. We are the global market leader for implantable and extracorporeal blood pumps based on magnetic levitation technology. Our life-saving systems, which we develop and manufacture in Zurich, are used for advanced heart failure patients needing short- or long-term circulatory support. Our location in the heart of the city of Zurich has around 130 employees in the areas of development, quality and production of the CentriMag system and the HeartMate 3. Currently, we are expanding our innovative team in Zurich and an exciting opportunity exists for a motivated and talented: MANUFACTURING ENGINEER – CHANGE MANAGEMENT Become part of a great team which is responsible for establishing and maintaining processes along the entire supply chain and manufacturing of life-supporting medical devices which are based on the fascinating technology of magnetic levitation. With your work you’ll ensure our products and processes meet the high standards of our industry and are in line with our policy “built as intended for your family”. In your role you will be interfacing and collaborating with cross-functional teams in Switzerland and the USA and various suppliers. Main Responsibilities: Manage Change Orders in the PLM software (Windchill), ensuring workflow is correctly applied. Drive the implementation of changes. Make sure timelines are held. Support the documentation of the impact analysis for Change Orders in PLM. Make updates to production documents, such as part specifications, or procedures and drive the continuous improvement of these documents. Present changes to affected audiences and perform training sessions. Work with other departments to gather feedback, inputs, and buy in for Change Orders and present changes to the Change Impact Board (cross functional team). Make sure parts are set up correctly in the ERP system (SAP) Guide and train Engineering and other functional users in the use of PLM system and change processes. Support process and system improvements for the PLM software and the change process. Required Qualifications: You have a basic technical training or degree You have 0-5 year(s) of professional experience in a regulated environment, preferably medical devices. Proficiency in English with excellent technical writing skills Excellent communication skills and ability to explain complex topics in a correct and concise manner Detail-oriented with strong time management skills and ability to meet strict deadlines You are proficient in MS Office and have experience with a PLM and ERP system. You collaborate well with other departments, such as Quality, Manufacturing, R&D, Project Management, Purchasing, Planning or suppliers. You have a conscientious, and well-structured way of working with a high degree of ownership. You prioritize your work according to business needs. Preferred Qualifications: German would be an asset Familiarity with Windchill or SAP would be an asset. Experience in change management and training system would be an asset. Knowledge of the regulations applicable in medical technology (ISO 13485 / FDA 21CFR Part 820 / GxP) is an asset. Experience in manufacturing of electronic products Working at Abbott At Abbott, you can do work that matters and help people to live a healthier and fuller life, grow your career, and learn, be your true self. You will have access to: Career development with an international company where you can grow A workplace in a fortune 500 company and the world’s leading manufacturer of medical devices A challenging position in a crisis independent industry To become part of a dynamic, highly educated, highly skilled, and motivated team Multi-national environment, where we foster the development of our talents within the enterprise Competitive compensations and benefits A workplace in the heart of Zurich We are looking for highly motivated person who would like to be part of our passionate team with broad responsibilities. Do you have what it takes? Then send us your application including motivation letter, curriculum vitae, letter of recommendation and diplomas today. We are looking forward to meeting you in the heart of Zurich! Please follow our Career site and check for available openings: Abbott Jobs | Apply Now | Abbott Laboratories Careers The base pay for this position is N/A In specific locations, the pay range may vary from the range posted. JOB FAMILY: Manufacturing DIVISION: HF Heart Failure LOCATION: Switzerland : Technoparkstrass 1 CH 8005 ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Not Applicable Abbott is about the power of health. For more than 125 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of life’s greatest health challenges. We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. Follow Us: Facebook LinkedIn YouTube TwitterÜber das Unternehmen:3363 Thoratec Switzerland GmbH

Manufacturing Engineer Manufacturing Engineer (all genders) We are mission critical Beyond Gravity, mit Hauptsitz in Zürich (Schweiz) ist das erste Startup, das Agilität, Geschwindigkeit und Innovation mit jahrzehntelanger Erfahrung und bewährter Qualität verbindet. Rund 1600 Mitarbeitende an 12 Standorten in sechs Ländern (Schweiz, Schweden, Österreich, Deutschland, USA und Finnland) entwickeln und fertigen Produkte für Satelliten und Trägerraketen mit dem Ziel, die Menschheit voranzubringen und die Erforschung der Welt und darüber hinaus zu ermöglichen. Beyond Gravity ist die bevorzugte Lieferantin von Strukturen für alle Arten von Trägerraketen und führend bei ausgewählten Satellitenprodukten und -konstellationen im New Space Bereich. Das Weltraum-Wissen nutzt Beyond Gravity auch für Anwendungen ausserhalb der Raumfahrttechnologie: Die hochpräzisen Produkte kommen bereits seit über 20 Jahren in der Halbleiter-Industrie zum Einsatz. Als Manufacturing Engineer bist du die Hauptschnittstelle zwischen der Entwicklung und der Produktion. Du planst die Ausführung aller Manufacturing, Assembly, Integration & Testing Aktiviäten, treibst die Ausführung dieser Tätigkeiten proaktiv mit voran und berichtest direkt an die Projektleitung. In Entwicklungsprojekten bist du für den Transfer von der Entwicklung in die Produktion zuständig, stellst die Herstellbarkeit sicher und definierst skalierbare Produktionsprozesse für zukünftige Serienproduktionen. Deine Aufgaben in dieser spannenden Rolle sind Planung, Koordination und Überprüfung von Projektarbeiten im Bereich Manufacturing, Assembly, Integration & Testing (MAIT) Konzeption und Optimierung von Produktionsprozessen, -vorrichtungen und Werkstückträgern für hochpräzise Mechanismen in Zusammenarbeit mit der Konstruktion, z.B. für Montage, Verkabelung, Klebeprozesse oder Reinigung Unterstützung der Konstruktion hinsichtlich Herstellbarkeit und Design-to-Cost Bedarfsplanung im SAP gemäss Kundenforecast Bereitstellung, Inbtriebnahme und Übergabe der Vorrichtungen und Werkzeuge an die Produktion Einhaltung der Produktqualität, z.B. durch entsprechende Vorschriften, Inspektionen und Procedures (Cleaning, Assembly & Testing) Vorantreiben der Fehlerbehebung in der Produktion. Der Manufacturing Engineer ist die erste Anlaufstelle für die Montage- und Prüftechniker Verantwortung für die zeitgerechte Abarbeitung von NC’s in den zugeteilten Projekten in Zusammenarbeit mit dem Product Assurance Zuständigen MAIT Schnittstelle zum Projektleiter, inklusive regelmässigem Reporting und Status-Updates Kontinuierliche Verbesserung der Prozessfähigkeit, Qualität und Effizienz Unterstützung des Einkaufs bezüglich Einhaltung der technischen Spezifikationen und Termine bei komplexeren Beschaffungen Technischer Support bei Fragen seitens der Lieferanten Analyse technischer Problemstellungen und Erarbeitung entsprechender Lösungen Unterstützung von technischen Angebotsarbeiten und Durchführen von Aufwandsschätzungen Präsentation von durchgeführten MAIT Arbeiten, auch vor Kunden Das folgende Profil bringst du mit Studienabschluss FH in Maschinenbau oder vergleichbar Mehrjährige Erfahrung (>5) in einem ähnlichen Aufgabengebiet (Produktion und Herstellverfahren) im Projektumfeld im Rahmen komplexer technischer Systeme in der Raumfahrt-, Medizinal- oder Halbleitertechnik-Industrie Erfahrung in der Definition von Produktionsprozessen Erfahrung in Fertigungstechnik und Grundkenntnisse in Werkstoffkunde von Vorteil Reinraumerfahrung oder Erfahrung mit Reinigungsprozessen von Vorteil Erfahrung mit Industrialisierungsprojekten und Prozessoptimierung von Vorteil Sehr gute mündliche und schriftliche Deutsch- und Englischkenntnisse SAP-Kenntnisse im Bereich PP/MM Fokus auf (interne) Kundenbedürfnisse Kreativ und lösungsorientiert mit einer Hands-on Mentalität Proaktive Kommunikation und Freude an der Arbeit in einem jungen und dynamischen Team Gute Organisations- und Koordinationsfähigkeiten und Durchsetzungsvermögen Hohe Stressresistenz und Ausdauer Was wir Dir anbieten Arbeit in einem internationalen Umfeld mit globaler Denkweise und High-Tech-Produkten Ein hoch spezialisiertes und motiviertes Team mit viel Know-how in einer einzigartigen Branche Wir leben eine Hands-on-Mentalität und nehmen Verbesserungsvorschläge ernst Attraktive Arbeitsbedingungen (Zuschuss zu öffentlichen Verkehrsmitteln, Schulungen und Entwicklungsmöglichkeiten, voll bezahlter Mutterschafts-/Vaterschaftsurlaub und vieles mehr) Flexibles und mobiles Arbeiten und mindestens 5 Wochen Urlaub mit der Möglichkeit, zusätzlichen Urlaub zu nehmen Dein Kontakt Haben wir dein Interesse an dieser spannenden Stelle geweckt? Dann freuen wir uns auf deine Online-Bewerbung. Recruiter/HR Manager: Stefan Hunger | https://beyondgravity.com Location: Zürich, ZH, CH Job Experience Level: Professionals Job Category/Job Family: Production Req ID: 6576

Manufacturing Engineer Satellites Mechanisms (all genders) Manufacturing Engineer Satellites Mechanisms (all genders) We are mission critical Beyond Gravity, headquartered in Zurich, Switzerland, is the first startup to combine agility, speed and innovation with decades of experience and proven quality. Around 1600 employees at 12 locations in six countries (Switzerland, Sweden, Austria, Germany, USA and Finland) develop and manufacture products for satellites and launch vehicles with the goal of advancing humankind and enabling the exploration of the world and beyond. Beyond Gravity is the preferred supplier of structures for all types of launch vehicles and a leader in selected satellite products and for constellations in the New Space sector. Beyond Gravity also uses its space knowledge for applications outside of space technology: The high-precision products have already been used in the semiconductor industry for more than 20 years. Your responsibilities Plans, coordinates and reviews project work in Manufacturing, Assembly, Integration & Testing (MAIT) Is the MAIT I/F to project management: He/she regularly updates and reports the manufacturing status to the project manager and the project team as well as customer if needed Supports Design wrt. Manufacturability and design-to-cost (e.g., holds regular reviews in front of CAD with design, procurement and suppliers during design phase, checks internal manufacturability together with the assembly & test technicians) Estimates the required production time and ressources for initial models and non-recurring activities. Defines the projects material demands (incl. Jigs & Tools) according to customer forecasts, sales orders or inputs from project management Is document owner of the MAI Plan (including flows and layouts) and assembly procedures Drives trouble shooting within production. Is the first point of contact for the Assembly & Test Technicians Continuously improves process capability, quality and efficiency Advises procurement and suppliers on technical questions (1st level support, 2nd level à Engineering) Your Profile University degree or technical college degree in mechanical engineering, industrial engineering or similar Hands-on mentality Customer – and service-orientation Strong communication skills 2+ years of previous hands-on Engineering experience in a more complex manufacturing setting. Space or Aerospace experience, or other regulated industries, such as medical devices or semiconductor industry Experience in manufacturing technologies and basic knowledge of materials science are an advantage SAP know-how Know-how in lean manufacturing or operational excellence Experience with MES, CAD and other relevant complex software What we offer Work in an international environment with global mindset and high-tech products that will fly into space A highly specialized and motivated team with a lot of know-how in a unique industry We live a hands-on mentality and take suggestions for improvement seriously Attractive employment conditions (contribution to public transport, trainings and development opportunities, full paid maternity/paternity leave and many more) Flexible and mobile working and at least 5 weeks of vacation with possibility to buy additional vacation Your contact Did we spark your interest in this exciting position? Then we look forward to receiving your online application. Recruiter/HR Manager: Stefan Hunger | https://beyondgravity.com Location: Zürich, ZH, CH Job Experience Level: Professionals Job Category/Job Family: Engineering Req ID: 6636

Manufacturing Engineer / Change Management Thoratec Switzerland GmbH is part of the medical device division of Abbott Laboratories, a fortune 500 company with over 115’000 employees worldwide. We are the global market leader for implantable and extracorporeal blood pumps based on magnetic levitation technology. Our life-saving systems, which we develop and manufacture in Zurich, are used for advanced heart failure patients needing short- or long-term circulatory support. Our location in the heart of the city of Zurich has around 130 employees in the areas of development, quality and production of the CentriMag system and the HeartMate 3. Currently, we are expanding our innovative team in Zurich and an exciting opportunity exists for a motivated and talented: MANUFACTURING ENGINEER – CHANGE MANAGEMENT Become part of a great team which is responsible for establishing and maintaining processes along the entire supply chain and manufacturing of life-supporting medical devices which are based on the fascinating technology of magnetic levitation. With your work you’ll ensure our products and processes meet the high standards of our industry and are in line with our policy “built as intended for your family”. In your role you will be interfacing and collaborating with cross-functional teams in Switzerland and the USA and various suppliers. Main Responsibilities: Manage Change Orders in the PLM software (Windchill), ensuring workflow is correctly applied. Drive the implementation of changes. Make sure timelines are held. Support the documentation of the impact analysis for Change Orders in PLM. Make updates to production documents, such as part specifications, or procedures and drive the continuous improvement of these documents. Present changes to affected audiences and perform training sessions. Work with other departments to gather feedback, inputs, and buy in for Change Orders and present changes to the Change Impact Board (cross functional team). Make sure parts are set up correctly in the ERP system (SAP) Guide and train Engineering and other functional users in the use of PLM system and change processes. Support process and system improvements for the PLM software and the change process. Required Qualifications: You have a basic technical training or degree You have 0-5 year(s) of professional experience in a regulated environment, preferably medical devices. Proficiency in English with excellent technical writing skills Excellent communication skills and ability to explain complex topics in a correct and concise manner Detail-oriented with strong time management skills and ability to meet strict deadlines You are proficient in MS Office and have experience with a PLM and ERP system. You collaborate well with other departments, such as Quality, Manufacturing, R&D, Project Management, Purchasing, Planning or suppliers. You have a conscientious, and well-structured way of working with a high degree of ownership. You prioritize your work according to business needs. Preferred Qualifications: German would be an asset Familiarity with Windchill or SAP would be an asset. Experience in change management and training system would be an asset. Knowledge of the regulations applicable in medical technology (ISO 13485 / FDA 21CFR Part 820 / GxP) is an asset. Experience in manufacturing of electronic products Working at Abbott At Abbott, you can do work that matters and help people to live a healthier and fuller life, grow your career, and learn, be your true self. You will have access to: Career development with an international company where you can grow A workplace in a fortune 500 company and the world’s leading manufacturer of medical devices A challenging position in a crisis independent industry To become part of a dynamic, highly educated, highly skilled, and motivated team Multi-national environment, where we foster the development of our talents within the enterprise Competitive compensations and benefits A workplace in the heart of Zurich We are looking for highly motivated person who would like to be part of our passionate team with broad responsibilities. Do you have what it takes? Then send us your application including motivation letter, curriculum vitae, letter of recommendation and diplomas today. We are looking forward to meeting you in the heart of Zurich! Please follow our Career site and check for available openings: Abbott Jobs | Apply Now | Abbott Laboratories Careers

Creoptix is an innovative, fast-growing brand of Malvern Panalytical located in Wädenswil near Zurich (Switzerland). Our mission is to enable life scientists to accelerate discovery by providing innovative tools for molecular interaction analysis. Our instruments are used in life science research labs within academia and industry. To strengthen our team, we are looking for a Manufacturing Engineer to join our team at Creoptix to help us make a significant difference in how we make the tools that measure the small things. Position: Manufacturing Engineer 100% Department: Supply Chain and Operations Location: Wädenswil, Switzerland Do you enjoy unravelling problems and making life more efficient? Are you looking for a role where you can own and improve production processes to make life easier for those who do them? Do you want to do this in an ambitious, fast-growing, international company with a friendly and inclusive culture? Then this is the job you are looking for! Responsibilities? Your Task will be Resolve engineering challenges to production targets using structured problem-solving tools like A3PS, 8D and DMAIC in collaboration with various key stakeholders. Maintain and control manufacturing processes using lean tools including Standard Operating Procedures, Bills of Materials (BOMs), Control Plans, Value Stream Maps, Kanban, and Process Failure Mode Effect Analyses (PFMEAs). Drive, validate and implement changes to product design with a focus on quality and manufacturability, to make sure that both new and existing products can be made, assembled and tested to the right specifications. Improve Key Performance Indicators (KPIs) in your technology through targeted projects and communicate project progress to key stakeholders in production and the wider business. Work with cross functional teams across the business to improve safety, quality and delivery of our market leading products. Complete sustaining activities to mitigate risks, manage costs, improve efficiencies, ensure our products remain relevant with regards to technological advancements and always continue to satisfy our customers needs. Support other operational teams to ensure that we can get the parts we need to make our products to the standard our customers want. Liaise with suppliers and our supplier quality team to resolve quality or delivery issues, as well as support supplier validation and reallocation processes. Own and develop cell and line layout and workstation design to make our processes the best and easiest they can be. What we expect To be successful in this role, you have: Mechanical Engineering or Manufacturing degree. 3 years plus experience in a similar role. Good understanding of electrical and mechanical engineering principles An enthusiasm for manufacturing processes A hands-on approach to solving challenging engineering/manufacturing problems Fluent English; excellent communication and presentation skills; an ability to influence at all levels of the organisation. Ability to manage your own time and workload to be able to balance responding quickly to immediate production issues with longer term improvement opportunities A collaborative mindset to be able to contribute to and pull together with different teams across the business Great to have: Experience in a high technology manufacturing or assembly business. Proficient level of German (spoken and written). Six sigma toolset and experience to tackle problems in a data driven way A vision for how modern manufacturing should be. Ability to analyse mechanical/electronic designs to suggest improvements to performance or manufacturability. Ability to gather and interpret information from multiple database sources, to analyse data and present conclusions. SAP or a similar ERP system experience. PLM and ECN system experience. 3D Mechanical CAD or PCB design abilities. Experience of manufacturing transfer. Driven both to deliver results for our customers and to develop yourself. Quality informed decision-making skills. What we offer Creatively innovative, supportive, and collaborative team. A fast-learning curve in an exciting, challenging, and open environment, where you will work within an interdisciplinary team First-hand exposure to the life science industries, including pharma and biotechnology To be part of Malvern Brand that is steadily disrupting an industry that is experiencing exponential growth. An opportunity to be part in developing the next generations of products that will be used for accelerating design of novel medicines. Potential for professional development in line with the growth of the company Comprehensive and competitive package, commensurate with background and experience. A great atmosphere, modern offices, lots of green and the lake nearby When you join? We value entrepreneurship and commitment by offering real career possibilities. You become part of a growing company where you can shape the future of our work processes. Occasional travel. By building a culture of respect and appreciation, we give everyone who works here the opportunity to realise their full potential. YES, I WANT THIS JOB!! Please click on apply. #LI-MG1 About us When you make the invisible visible, the impossible is possible. Our analytical systems and services help our customers to create a better world. Through chemical, physical and structural analysis of materials, they improve everything from the energies that power us and the materials we build with, to the medicines that cure us and the foods we enjoy. We partner with many of the world’s biggest companies, universities and research organizations. They value us not only for the power of our solutions, but also for the depth of our expertise, collaboration and integrity. With over 2200 employees, we serve the world, and we are part of Spectris plc, the world’s leading precision measurements group. We are Malvern Panalytical. We’re big on small. Malvern Panalytical is committed to diversity and inclusion. We are dedicated in providing a safe and healthy working environment where employees succeed. We prohibit discrimination and harassment against staff and applicants and do not discriminate on the basis of race, color, nationality, ethnicity, sex, gender reassignment, sexual orientation, disability, religion, age or belief Search open positions that match your skills and interest. We look for passionate, curious, creative and solution-driven team players We invite you to share your details with us today! We will be in touch to discuss potential opportunities with you. We are Malvern Panalytical. We're BIG on small. We are here to unleash the power of very small things, to make big things happen. Our technologies enable our customers to create a better world. Improving everything from the energies that power us and the materials we build with, to the medicines that cure us and the foods we enjoy. We partner with many of the world’s biggest companies, universities and research organizations. They value us not only for the power of our solutions, but also for the depth of our expertise, collaboration and integrity. We are a globally diverse mix of visionary thinkers, creative problem-solvers, and detail-loving geeks. United by knowing that when you can make the invisible visible, you make the impossible possible. Value beyond measure. We are a diverse team from all over the world: scientists and engineers. Thinkers and doers. Big picture visionaries and detail-loving geeks. We’re all different – though together, we share common values that guide us every day. Our values help shape our high-performing culture and hold each other to high standards in everything we do.Über das Unternehmen:Creoptix AG

Atracsys is a Swiss company specialized in leading-edge 3D/6D optical pose measurement systems for medical, research, education and industrial applications. The primary focus being on robotic and computer assisted surgery (CAS) systems. In 2019 Atracsys joined the Smith+Nephew Group, a portfolio medical technology business with +18´000 employees worldwide. To further grow our business in Puidoux (VD) we are looking for a: Manufacturing Engineer (f/m/x) Purpose of this role: Work closely with internal development/manufacturing teams and suppliers, to transfer products to manufacturing. Improve and stabilize existing manufacturing processes, to insure capacity and quality. What you will do: Definition and validation of manufacturing process (Mechanical assembly, special process, etc.) Definition and validation of manufacturing tools Writing of work instructions and production specifications Conduct process related risk management activities Manage and write design transfer documentation Conduct continuous improvement on process, and on Qualification and Validations projects Support on Non-Conformity handling, CAPA, external audits and failure investigations Work closely with the R&D team to secure prototypes Provide training to subcontractor To be successful in this job you need: Engineering degree (BSc/MSc) in mechanical, electronical, microengineering or manufacturing related field (HES/EPF or equivalent) 3-5 years of experience in similar role Applied technical understanding of manufacturing equipment; processes specific to medical device manufacturing preferred Experience with electronic system and manufacturing processes of advantage Experience with medical QMS, ISO13485 of advantage Fluent in French and English mandatory, German is a plus We offer: An interesting and varied function in an international company Modern infrastructure and opportunities to further advance your career The opportunity to play a relevant part in a medical network and to further develop a company with an excellent reputation Attractive compensation package and social benefits Flexible work time models A great team in a great atmosphere Do you feel addressed? Then we would like to get to know you. Please send your application (PDF) via our career portal. Smith & Nephew, Lars Thomann, Talent Acquisition Specialist #LI-LT1 Atracsys LLC, Route du Verney 20, 1070 Puidoux, Switzerland, www.atracsys.com Stay connected and receive alerts for jobs like this by joining our talent community. We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day. Check our Glassdoor page for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N. Explore our new website and learn more about our mission, our team, and the opportunities we offer. Smith+Nephew is a global medical technology company. We design and manufacture technology that takes the limits off living. We support healthcare professionals to return their patients to health and mobility, helping them to perform at their fullest potential. From our first employee and founder, T.J. Smith, to our team today, it’s our people who make Smith+Nephew a unique place. Yes, we love to innovate and develop exciting technologies, and we offer competitive salaries and progressive benefits. But it’s our culture - of Care, Collaboration and Courage - that really sets us apart. Through a spirit of ownership and can-do attitude we work together to win. We’re a company of people who care about each other, about our customers and their patients, and about our communities. Together, we fulfill our shared purpose of Life Unlimited. 165 years of pioneering innovation requires a relentless focus on what’s next. We’re focused on you. You’re what’s next...Ready to take your career to the next level? Join our talent community for access to new job opportunities. Sign up now!Über das Unternehmen:CHE - Atracsys Sarl

Für unseren Kunden aus der Nähe von Aadorf (TG) suchen wir Sie als Manufacturing Engineer m/w/dIHRE AUFGABENKonzeptionierung, Planung und Optimierung von Produktionsanlagen und Produktionsprozessen mit dem Schwerpunkt AutomatisierungOptimierung hinsichtlich Anlagenverfügbarkeit und ProzesssicherheitUnterstützung der Instandhaltung und Koordination relevanter DienstleistungenZusammenarbeit mit dem Produktions- und Engineering-TeamProjektmanagementIHR PROFILStudium mit technischem Schwerpunkt oder technische Berufsausbildung mit der Weiterbildung zum Techniker oder IngenieurMindestens drei Jahre Berufserfahrung in einer vergleichbaren PositionFundierte theoretische und anwendusorientierte FachkenntnisseFähigkeit zum analytischen DenkenStrukturierte Herangehensweise an HerausforderungenGute technische AllgemeinbildungKommunikationsstärkegute Englischkenntnisse in Wort und SchriftUNSER ANGEBOTWir bieten Ihnen einen sicheren Arbeitsplatz in einem expandierenden Unternehmen. Sie erwartet ein angenehmes Arbeitsklima in einem motivierten Team und ein Arbeitsumfeld, das durch Offenheit und gestalterischem Freiraum überzeugt. Die schnelle Übernahme von Verantwortung in einem spannenden Aufgabengebiet wird durch flache Hierarchien und kurze Entscheidungswege unterstützt. Wir wertschätzen Vielfalt und begrüssen daher alle Bewerbungen – unabhängig von Geschlecht, sozialer Herkunft, Religion/Weltanschauung, Alter und Identität.Dies ist genau das, was Sie als neue Herausforderung suchen?Dann freuen wir uns auf Ihre Bewerbung vía ButtonBei weiteren Fragen Sie uns gerne unter +41 (0)41 520 01 31 kontaktieren.Andere haben sich auch angeschautMehr InformationenName: ShareThisAnbieter: ShareThis, Inc.Zweck:Dieses Marketing-Cookie wird von der ShareThis-Plattform bereitgestellt und ermöglicht es unseren Besuchern, Inhalte unserer Website in sozialen Medien zu teilen. Durch die Aktivierung dieses Cookies können wir das Teilen von Inhalten in sozialen Netzwerken erleichtern und unsere Online-Präsenz stärken. Dies dient dazu, unsere Website und unsere Inhalte einem breiteren Publikum zugänglich zu machen. Weitere Infos: SpeichernAlle ablehnenManufacturing Engineer80 - 100% 2024-03-16 85000.00 / YEAR CHF 16-01-2024 Aadorf (TG) Sie möchten Ihre Expertise als Manufacturing Engineer gezielt in einer neuen beruflichen Herausforderung unter Beweis stellen, um Ihr Potential voll ausschöpfen zu können? Dann gehen Sie jetzt mit uns Ihren nächsten Schritt! Technical-jobs.ch, als Teil der bruederlinpartner-Gruppe, bringt als spezialisierter Personaldienstleister jeden Tag Fach- und Führungskräfte im Maschinen-und Anlagenbau mit nationalen und internationalen Unternehmen zusammen. Nutzen Sie unsere persönlichen Kontakte zu Arbeitgebern schweizweit! Wir empfehlen Sie an unsere Kunden weiter und erleichtern Ihnen damit den Einstieg ins Unternehmen!

Lean manufacturing engineer Description du poste Pour notre client spécialisé dans les technologies médicales, englobant divers secteurs chirurgicaux tels que l'orthopédie, la neurochirurgie, la chirurgie générale et reconstructive, nous recherchons un(e) : Ingénieur/technicien en Lean Manufacturing (contrat temporaire indéterminé) Au sein du département d'amélioration continue vous intervenez en tant que professionnel en Lean manufacturing.Vous possédez une expertise dans la gestion des fournisseurs car ce rôle vise à conduire des améliorations chez nos fournisseurs en soutenant et améliorant les résultats de notre usine. Responsabilités Soutien des activités quotidiennes liées au programme d'amélioration continue, notamment les idées d'amélioration des processus en attente de mise en oeuvre chez les fournisseurs. Identification constante d'opportunités d'amélioration avec les fournisseurs afin de simplifier les flux. Soutien aux cellules de production et rôle de point de contact pour la fabrication Lean lors des revues de performances. Fourniture de soutien d'assurance qualité à des sites de fabrication sous contrat et aux fournisseurs de matières premières impliqués dans la production de nos produits. Soutien au processus d'accord qualité avec les fournisseurs concernés par la production de nos produits. Rapport sur les indicateurs de performance des fabricants sous contrat. Assurer un soutien technique aux départements QC, achats et production. Fournir un soutien en ingénierie qualité aux fournisseurs, y compris des activités de vérification/validation et de gestion des changements. L'accent sera mis sur les réglementations/normes FDA CFR partie 820 et ISO 13485. Traitement des demandes de changement de fournisseur conformément aux procédures et aux exigences réglementaires. Veiller à ce que les activités de validation des processus/produits externalisés soient réalisées et documentées selon les procédures et dans les délais définis. Signalement des problèmes de qualité des fournisseurs à la direction, le cas échéant, et proposition de solutions robustes et conformes. Participation aux projets qualité au besoin. Soutien aux enquêtes sur les plaintes, selon les besoins. Profil Diplôme de bachelier en génie, sciences de la vie ou une discipline technique connexe est requis. Les candidats avec une combinaison équivalente d'éducation et d'expérience seront également pris en considération. Une expérience de travail dans un environnement de fabrication de dispositifs médicaux est préférable. Une expérience en qualité fournisseur opérationnelle est préférée, ainsi qu'une expérience Lean. La certification Lean ou Six Sigma est un plus. Un minimum de 2 ans d'expérience professionnelle dans une industrie réglementée GMP et/ou ISO est requis. Connaissance des normes et réglementations des dispositifs médicaux telles que ISO13485, 93/42 EEC, 21 CFR partie 820. Utilisation de systèmes ERP, PLM. Expérience ou connaissance des processus d'usinage, de moulage par injection et/ou de composants/assemblages électromécaniques est préférée. Maîtrise du français et de l'anglais. Margot Ferraton

Wir sind auf der Suche nach einem engagierten Process & Manufacturing Engineer (m/w/d), der/die die Verantwortung für die Sicherstellung der Prozessstabilität übernimmt, notwendige Verbesserungsmassnahmen entwickelt und Prozessoptimierungen definiert und umsetzt.Process & Manufacturing Engineer (m/w/d) 100%Ihre HerausforderungSicherstellung der Prozessstabilität und Entwicklung notwendiger VerbesserungsmassnahmenDefinieren und Umsetzen von ProzessoptimierungenStrukturiertes und selbstständiges Analysieren und Optimieren betreuter FertigungsprozesseSicherstellen der technischen AnlagenverfügbarkeitEvaluieren, realisieren und optimieren neuer Technologien und Prozesse im Bereich FolienproduktionIdentifizieren und Koordinieren von Projekten zur Optimierung der Kosten-, Ausschuss- und Qualitätssituation sowie zur Reduktion der DurchlaufzeitUnterstützung bei der Beschaffung und Kostenplanung entsprechender Komponenten, Teilsysteme und AnlagenMitverantwortlich für die Schulung der Operatoren sowie Erstellung und Aktualisierung von Anleitungen und PrüfvorschriftenFachliche Unterstützung bei Fehlerrückverfolgung, Qualitätsmassnahmen und Qualitätsbeanstandungen sowie bei der ProduktentwicklungIhre KompetenzAbgeschlossenes Studium in Maschinenbau, Verfahrenstechnik, Automatisierungstechnik, Materialwissenschaften, Wirtschaftsingenieurwesen oder als ProduktionsingenieurErfahrung im Projektmanagement, vorzugsweise in der IndustrieGute Kenntnisse in statistischer Prozesskontrolle und Datenanalyse mittels statistischer SoftwareVerhandlungssicheres Deutsch und EnglischIhre PerspektivenEin dynamisches Arbeitsumfeld in einem innovativen UnternehmenDie Möglichkeit, an herausfordernden Projekten mitzuarbeiten und Ihre Fähigkeiten kontinuierlich weiterzuentwickelnAttraktive Vergütung und BenefitsEin freundliches und motiviertes Team, das Sie unterstützt und fördert