Gehaltsübersicht für Medical Device in Schweiz
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Gehaltsübersicht für Medical Device in Schweiz
120 000 ₣ Durchschnittliches Monatsgehalt
Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "Medical Device in Schweiz"
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Medical Device Branche in Schweiz
Verteilung des Stellenangebots "Medical Device" in Schweiz
Wie die Grafik zeigt, in Schweiz gilt Kanton Zürich als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Kanton Waadt. Den dritten Platz nimmt Basel-Stadt ein.
Ranking der ähnlichen Stellenangebote gemäß dem Gehaltsniveau in Schweiz
Unter den ähnlichen Berufen in Schweiz gilt Master Data Manager als der bestbezahlte Beruf. Laut unserer Webseite beträgt das Durchschnittseinkommen 100000 CHF. An zweiter Stelle folgt Media mit dem Gehalt von 82500 CHF und den dritten Platz nimmt Mécanicien mit dem Gehalt von 80000 CHF ein.
Head of Robotic Surgical Instrumentation (Medical Device)
Coopers Group AG, Waadt
Lead the team (5 persons) in charge of robotics surgical instruments development, associated single use Accessories and support product development, for minimally laparoscopic invasive procedureStrategize and manage instruments team and resources, covering people development, capacity, access to development tools and scheduling development activities.Contribute to the Company’s product management effort, aligning product roadmap with customer expectations. Ensure delivery of robotic surgical instruments and accessories in a timely manner according to the Company’s product roadmapDrive risk management activities (identification, assessment, prioritization, and risk control) for all instruments development and participate to overall project risk management activitiesEnsure compliance with relevant norms (ISO 13485, ISO 14971, IEC 62304, IEC 60601-1)Your profile:Engineering degree in Mechanical/Micro-Engineering/Biomechanics/Biomedicine (or Material Sciences)Proven track record as Team Leader/Manager/Head of Department of complex Medical Devices/Robotics Surgical Instrumentation/Accessories: MandatoryExperience working in the field of Endoscopy, Laparoscopy, ENT (Otorhinolaryngology/Ear, nose and throat medicine)Strong experience in Designing (CAD/CAO) & developing instrumentation for high production volume (100’000/year)Experience partnering with external suppliers for the development of new processes and technologies with proven knowledge on biocompatibility and sterilization (choice of materials) / New Product Introduction/IndustrializationProven track record of leading, coaching, mentoring and managing a team of engineersVersatile, all-purpose, hands-on, solution-oriented, maker spiritAgile/Scrum project management skills : an assetEnglish Fluent. French or German: a strong asset
QA engineer Pharma Biotech Medical Device
CAPGEMINI, Lausanne, Switzerland
With over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Altran deploys its expertise particularly in: - Life Sciences (Pharma, Biotech, and Medical Devices), - Industry, Aerospace, Automotive, Energy, Railways, - Financial Services: P&C Insurance, Health Insurance, Reinsurance, Banking - Telecoms - Public sector Our offerTo strengthen our team in Switzerland we are looking for Quality Assurance Consultants. As a Quality Consultant you will provide our clients with the necessary expertise and assistance to further improve and maintain the quality standards for their operations and products. QA engineer Pharma Biotech Medical Device Your role You will be involved in: - Initiating improvements to the Quality Management System, ensuring compliance to all relevant quality standards and regulatory requirements.- Handling customer complaints.- Investigating deviations and non-conformities in cross-functional teams.- CAPA and risk analysis- Reviewing batch records and release. - Review and proactively assist in process capability studies and statistical techniques as required, to support continuous improvement. Your profile Education level: Master or Engineering Degree in quality engineering (EPFL, ETH, HES or equivalent) with emphasis on Pharma- and/or Biotech- and/or Medical Engineering. Requirements: - Minimum 2 years of experience in Quality Assurance.- Applied knowledge of FDA or Swissmedic and international Pharmaceutical and or medical device regulations (ISO 13485, 21 CFR 820, etc.).- Applied technical understanding of manufacturing equipment; processes specific to pharmaceutical, biotech and or medical device manufacturing. Languages: French and English fluent mandatory. Key qualities: - You know how to take initiative- You like to work in a multidisciplinary team- You value knowledge-sharing- You must have strong verbal and writing communication capabilities.
Senior Director Medical Device Program Lead m/f
Michael Page, Lausanne
* Lead definition of device development strategy in partnership with key internal stakeholders. Ensure implementation of Quality Management System.* Lead cross-functional exercises to define targeted device profiles.* Develop device development project plans and budget with internal and external cross functional teams.* Deliver quality products and processes with appropriate validation and regulatory documentation.* Report and tightly control device development timelines, budget and risks to biosimilars project development team.* Act as the main interface between the biosimilars project development teams and the subteams (e.g. medical devices, manufacturing & supply, etc.) as well as device vendors.* Provide technical and business inputs to projects. Analyze risks and suggest mitigation plans.* Oversee device development, manufacturing, validation and regulatory activities.* Proactively anticipate and identify risk areas and alert stakeholders appropriately.* Report and escalate to management potential issues as needed.* Identify new device opportunities* Bachelor's degree (or equivalent) in an applicable Product design, Mechanical, Process, Materials Science or Electronic Engineering field.* 5+ years of experience in project management* 10+ years of experience in device development with an understanding of device safety, regulatory requirements, policies and procedures.* Deep technical understanding of device design, validation, verification and their link to other drug development activities (clinical, manufacturing, commercial, etc.) in the overall drug development plan.* Experience in FDA regulated medical devices, Standalone CE marked devices and combination drug device products.* Track record of resolving issues in a matrix organization.* Strong interpersonal and relationship building skills with the ability to establish a trusted role with the various stakeholders.* Solid organizational skills including attention to detail and multi-tasking skills.* Effective verbal and written communication.* Fluent in English, both oral and written; additional languages (German or French) are an asset.* Managerial experience
Sr Manager, Site Activation - Medical Device & IVD
Icon Clinical PLC, Basel, CH
Sr Manager, Site Activation - Medical Device and IVD ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. The Role: Prepare/co
Medical Device & Combination Product Development Project Manager (4489)
CTC Resourcing Solutions, Basel, Basel-Stadt
Medical Device & Combination Product Development Project Manager (4489) Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas. They are also into Combination Products and Medical Technology. For our client, we are looking for a Medical Devices & Combination Product Development Project Manager for a permanent role based in Basel, Switzerland. Main Responsibilities: Accountable and responsible for technical product development, end to end project management from concept to market launch to meet business objectives Provide sound project strategy, organization, budget, planning management, technical & engineering expertise to develop and introduce new product for clinical phase and commercial launch Accountable for timely execution of the allocated projects including alignment of cross functional deliverables (technical, quality, regulatory, operations, supply) Provide operational strategy and investment plan Provide technical, engineering, human factors, and operations expertise for medical devices & combination product for clinical phases and commercial launch Efficiently collaborate with all involved functions beyond core team (e.g. LCT, Marketing) Improve project management phase gate process, align with all stakeholders and deploy/train the organization accordingly Ensure compliance with all local, state, federal, and company quality policies, procedures and practices, safety regulations, policies, and procedures Elaborate overall projects strategy, phase gates to project plan and detail planning across functions Report project progress by means of key indicator implementation Lead joint core team meetings Lead supplier/partner relationship and leverage all possible partner/supplier knowledge and documentation to maximize efficiency while ensuring their regulatory readiness Elaborate operation strategy for clinical phase and product launch / continuity of supply in accordance to forecasts Effectively collaborate with all project functions and communicate technical requirement for development and industrialization of the product Qualifications and Experience: Minimum 10 years of experience in combination product project management, with 7 years demonstrated combination product project management in pharmaceutical industry Track record of successfully delivering combination products to market Proven track record of successfully leading combination product projects from planning to execution, preferably in the field of parenteral delivery systems (e.g. prefilled auto-injectors, pens, patch pump) Excellent project management skills and sound knowledge of cross-functional requirements (technical, human factor, quality, regulatory and operations/qualification-validation) Broad and deep understanding of disciplined product development processes, regulatory and quality requirements as well as GMP & ISO 13485 Strong persuading, influencing and negotiation skills Capability to successfully engage, collaborate and influence with different stakeholders at all levels of seniority Demonstrate agility and action orientation when facing change and uncertainty Excellent and communication skills in English (oral and written) Demonstrate agility and action orientation when facing change and uncertainty Excellent and communication skills in English (oral and written)
Medical Device Software Engineer
BestLogic Staffing, CH, Engi
Full time | BestLogic Staffing | United States Posted On 09/22/2021 Job Information Manufacturing Work Experience 5 years City Cambridge State/Province Massachusetts 02138 Job Description This Medical Device Software Engineer (Engineer) position will contribute to the design, implementation and verification of software for one or more of the projects we are bringing to market. It is a hands-on role that may include all aspects of device software development: firmware and software, algorithm development and optimization, image processing, application and GUI development. If you have Software Engineering experience, preferably in the medical device field, and want to use your expertise to build new, innovative products, this could be the job for you Responsibilities: Software analysis, planning, design, implementation, and verification of novel medical devices that consists of hardware control, data acquisition, signal/image processing, display, and post processing of medical images Work collaboratively with researchers and application development engineers in all software development phases Design and code medical-grade software that meet the defined software requirements and Design Inputs Create documentation adhering to quality procedures, regulations, standards and industry best practices under Design Control Contribute to product requirement development and risk management reviews Work effectively in cross-functional teams consisting of Research, Engineering, QA/RA, and Marketing Keep abreast of relevant and new technologies in the medical device field Report progress regularly to Senior Software Engineer Contribute to patent analysis and invention creations Requirements Qualifications: Education Required: Minimum Bachelor’s Degree in Computer Science or related discipline Experience Required: 3 years in a software engineering role with Medical Devices, Pharmaceuticals or Biotechnology industry. Direct experience of software architecture design and development is preferred Strong understanding of modern programming languages. Proficiency in C/C++ is required Must be a team player and possess strong oral and written communication skills Experience in one more of the following: Developing for MS Windows Developing medical or other safety-critical products Designing complex hardware control systems using UML or SysML (Rational or Enterprise Architect) Knowledge and experience in DICOM and 2D medical image processing; experience using toolkits such as IPP, ITK, VTK or 3D Slicer OpenGL, GPU/CUDA, OpenCV coding Prototyping with MATLAB, Simulink, LabVIEW Intellectual property development Requirements analysis and risk management processes, e.g. hazard analysis and dFMEA
Validation/Qualification Engineer - Medical Device
Michael Page, Biel
Your roleYou will oversee issues from the operation processes to the operation team and the site productionYou will be the representative during investigation including root cause analysis and health risk assessmentsYou will be in charge of executing validations, test method validations and all the other reports required.You will take part as support during supplier, internal/external auditsYou will initiate and lead project teams on non-conformance investigations regarding finished goods failures, product returns and component failuresYou will oversee technical support with customer complaints and product returnsYou will lead project teams on CAPA projectsYour Profile:Bachelor's degree in Industrial Engineering or equivalentTwo years of Quality Engineering experience, preferably in the medical device fieldExcellent understanding of investigation techniques including design of experiments and root cause analysisEnglish proficiency, fluent in German or FrenchProfessional IT Skills (MS Office etc.)
MDR Project Manager (Medical Device)
Experis AG, Solothurn, Switzerland
MDR Project Manager (Medical Device)For our client, Switzerland's leading medical device company, we are looking for a Project Manager with experience in the medical device industry and knowledge of MDR regulations. This is initially a 12-month contract, with extension possibility, based in the Solothurn area, Switzerland.Responsibilities:You will support the MDR compliance execution as project manager who has oversight on ongoing MDR compliance work for Trauma/CMF/BIO and drive completion of MDR deliverables. This activity includes but is not limited to:Coordinating and driving the resolving of NB questions to submitted Technical DocumentationProviding regular status updates on MDR compliance progress for Trauma/CMF/BIO to MDR PMO and governance team.Facilitating resolving of roadblocks and timeline constraints.Supporting the execution of project plan for MDR compliance in Trauma/CMF/BIO business for 2021/2022.Leading regular status update meetings with corresponding teams who are working on individual MDR files and/or specific topics.Leading and tracking cross-functional activities as assigned, such as MDR Indication definition and Technical Documentation submissions to Notified Body.Providing project management support for activities needed in preparation for MDR compliance as instructed and assigned.Must Haves:2+ years Project Management experience within the Medical Device industryBasic understanding of MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) 2017/745).Excellent person interaction skills and reliable and goal-oriented awork attitudeExperienced MS Office skills, especially in MS ProjectStrong analytical skillsNice to haves:GermanGeneral Information:Duration: initially 12 monthsExtension: possibleLocation: Canton Solothurn, SwitzerlandWorkload: 100%Interested in this opportunity? Kindly send us your CV today through the link in the advert. Should you have any questions please contact Nastasia Whyte.
Supply chain Assistant for an international medical device company
Academic Work Switzerland, Eysins, Switzerland
Supply chain Assistant for an international medical device company Tu as une première expérience en assistanat de projets supply chain et tu as un niveau d'anglais C1 minimum ? Tu es à l'aise avec la gestion de données ? N'hésite plus, nous avons l'offre parfaite pour toi ! À propos du rôle Notre client, un leader international des medical device est à la recherche d'un coordinateur supply chain pour participer aux différents projets des opérations supply. Tu t’adaptes vite et est capable de travailler de manière autonome ? Descriptif des tâches Assister les managers sur les aspects de reporting Collaborer avec les équipes supply chain opération en interne Extraction et analyse les données Classification et inventaire de documents Nous recherchons Expérience de minimum 2 ans en assistanat en supply chain, gestion des données idéalement dans un milieu international Diplôme en supply chain ou business administration Anglais courant, oral et écrit (C1 minimum) Personne ayant une organisation irréprochable, autonome, rigoureux et collaboratif Autres informations Possibilité de faire du télétravail
Senior Manager, Medical Device Safety
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. This is a global role which supports the Worldwide Patient Safety Vision through understanding the impact of daily work on all stakeholders of Safety Data Processing. This role provides oversight of quality and process optimization through a Business Partner Model working with mult