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Test Engineering Intern jobs at Boston Scientific in Canada, Montreal

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Canada
Montreal
13 jobs found
22.11.2025
BS

Boston Scientific Senior R&D Test Engineer / ingénieur principal en essais Canada, Quebec, Montreal

Limitless High-tech career opportunities - Expoint
Wsparcie działań GBS i Payroll w zadaniach administracyjnych w regionie EMEA. Utrzymywanie i aktualizacja treści wewnętrznych (np. FAQ) na portalu firmowym. Przygotowywanie i dostarczanie raportów zespołom wewnętrznym i interesariuszom. Organizowanie...
Description:

Opis stanowiska:

Poszukujemy Stażysty ds. Wsparcia Administracyjnego, który dołączy do naszych zespołów Payroll oraz Global Business Services (GBS), wspierając działania w krajach regionu EMEA. To idealna rola dla osoby, która lubi pracować z danymi, systemami i różnymi działami, zapewniając płynność procesów biznesowych. Będziesz zajmować się koordynacją informacji, dbaniem o spójność danych oraz wspieraniem narzędzi cyfrowych usprawniających pracę organizacji.

Twoje obowiązki:

· Wsparcie działań GBS i Payroll w zadaniach administracyjnych w regionie EMEA.

· Utrzymywanie i aktualizacja treści wewnętrznych (np. FAQ) na portalu firmowym.

· Przygotowywanie i dostarczanie raportów zespołom wewnętrznym i interesariuszom.

· Organizowanie i uzgadnianie danych na potrzeby raportowania i operacji.

· Weryfikacja i kontrola danych pracowników w systemach.

· Wsparcie testów i dokumentacji w ramach inicjatyw automatyzacji procesów.

Szukamy osoby, która:

· Jest w trakcie studiów licencjackich lub ukończyła kierunek administracja, języki lub pokrewne.

· Biegle posługuje się językiem angielskim i niemieckim (min. B2+). Znajomość innych języków będzie atutem.

· Posiada silne umiejętności organizacyjne i administracyjne.

· Dobrze zna pakiet Microsoft Office i szybko uczy się nowych systemów.

· Jest skrupulatna, analityczna i potrafi rozwiązywać problemy.

· Potrafi pracować samodzielnie oraz w zróżnicowanym, międzynarodowym środowisku.

· Dobrze zarządza czasem i priorytetami.

Oferujemy:

· Umowę stażową do 12 miesięcy, elastyczne godziny (30–40 godz./tyg.).

· Model hybrydowy (3 dni w biurze).

· Międzynarodowe środowisko pracy i wspierających współpracowników.

· Możliwość rozwoju umiejętności administracyjnych i koordynacyjnych w globalnej organizacji.

· Nowoczesne biuro w centrum Warszawy.

Lokalizacja: Warszawa (Hybrydowo)

Start: Grudzień/Styczeń 2025

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22.11.2025
BS

Boston Scientific Senior Manager Electrical Engineering / Canada, Quebec, Montreal

Limitless High-tech career opportunities - Expoint
Drive sales performanceby executing territory sales strategies and meeting or exceeding revenue and unit growth targets on a monthly, quarterly, and annual basis. Build strong relationships. Develop account strategies. Support...
Description:

About the role:

Rhythm Solutions division, you will be responsible for driving sales of the, a groundbreaking alternative to long-term anticoagulation therapy for patients with non-valvular atrial fibrillation.

In this dynamic field-based role, you will identify and grow new business opportunities, foster long-term customer relationships, and support procedural success through hands-on clinical expertise. You’ll work closely with electrophysiologists, interventional cardiologists, and hospital stakeholders to expand access to Watchman and make a measurable impact on patients’ lives.

Learn how Watchman is transforming patient care:

Your responsibilities will include:

  • Drive sales performanceby executing territory sales strategies and meeting or exceeding revenue and unit growth targets on a monthly, quarterly, and annual basis

  • Build strong relationships

  • Develop account strategies

  • Support implant proceduresclinically to understand physician preferences and ensure positive patient outcomes

  • Lead product education efforts, including in-services, product demos, and tailored presentations to hospital staff and clinicians

  • Develop pricing proposals

  • by identifying and implementing feasible, value-based solutions

  • Expand access within hospital systemsby identifying decision-makers and building new contacts across departments

  • Demonstrate strong clinical and technical aptitudewith deep understanding of Watchman device usage and procedural dynamics

Required qualifications:

  • Minimum of a bachelor’s degree in a related field

  • Minimum of 6 years of sales experience, ideally in medical devices calling on cardiology, cath/EP labs, or hospital-based environments

  • Proven success in territory development, sales growth, and customer relationship management

Preferred qualifications:

  • Master’s degree or MBA

  • Experience in structural heart, interventional cardiology, electrophysiology, or related industry

  • Prior experience supporting implantation procedures in cardiovascular or medical device settings

  • Technical aptitude and the ability to communicate complex product information clearly

  • Flexibility to work varied hours and complete a rigorous training program

The anticipated annualized base amount or range for this full time position will be$65,000, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.


For MA positions:It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.


Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.

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21.11.2025
BS

Boston Scientific R&D Test Engineer II / Ingénieur d'essai Canada, Quebec, Montreal

Limitless High-tech career opportunities - Expoint
Analyze system requirements to design and develop test plans and protocols to ensure designs meet requirements. Applies technical knowledge to innovate, design, and develop processes, procedures, fixturing and/or automation. Perform...
Description:

About the role

As an R&D Test Engineer II, you will play a crucial role in ensuring the quality and reliability of our medical device products. You’ll collaborate with cross-functional teams to design, develop, and execute comprehensive test plans, ensuring compliance with industry standards and regulations. Your work will directly impact patient safety and contribute to life-changing solutions.

Your responsibilities will include:

  • Analyze system requirements to design and develop test plans and protocols to ensure designs meet requirements.
  • Applies technical knowledge to innovate, design, and develop processes, procedures, fixturing and/or automation.
  • Perform engineering, functional and performance testing of electrical/electro-mechanical components, subsystems, and complete systems.
  • Monitor and analyze test results, generate detailed reports, and provide recommendations for improvement.
  • Provides Design for Manufacturability (DFM) and Design for Test (DFT) input to the engineering print package.
  • Work with a cross-functional team.
  • When required, provides work direction to technicians and may train test personnel when required as part of a validation.
  • Work independently to plan and schedule own activities necessary to meet timelines and communicate in a timely manner.
  • Other duties as required.

Required qualifications:

  • Bachelor’s degree in electrical engineering (or related field).
  • 3+ years of relevant experience relating to test systems development.
  • Understands engineering and problem-solving principles, concepts, tools, and techniques, as well as fundamentals of change management and test validation.
  • Develops creative solutions and collaboratively draws ideas from cross functional teams. Advocates for his or her ideas with passion while listening to and considering the ideas of the team.
  • Takes initiative to identify improvement opportunities, prioritize them, communicate them to the appropriate levels and sees them through to completion.
  • Is resilient in the face of setbacks. Plans appropriately for risks and responds positively to unforeseen problems.
  • Excellent organizational, communication and collaboration skills.
  • Strong documentation skills.

Preferred Qualifications:

  • Medical device industry background preferred
  • Equipment and fixture design, along with test systems development experience
  • Process Development; equipment validations and process characterization experience
  • Ability to translate theoretical and abstract ideas into meaningful innovation
  • LabVIEW and/or C/C++ programming experience
  • Experience with SolidWorks
  • Data driven individual; statistical analysis experience
  • Design experience; new product development
  • Experience with automation and programmable logic controllers

Vos responsabilités comprendront :

  • Analyser les exigences du système pour concevoir et développer des plans et protocoles d’essais afin de garantir que les conceptions répondent aux exigences.
  • Appliquer vos connaissances techniques pour innover, concevoir et développer des procédés, des procédures, des dispositifs de fixation et/ou des automatisations.
  • Effectuer des essais d’ingénierie, fonctionnels et de performance sur des composants électriques/électromécaniques, des sous-systèmes et des systèmes complets.
  • Surveiller et analyser les résultats des essais, rédiger des rapports détaillés et formuler des recommandations d’amélioration.
  • Fournir des commentaires sur la conception pour la fabricabilité (DFM) et la conception pour les essais (DFT) dans le cadre du dossier d’ingénierie.
  • Travailler avec une équipe multidisciplinaire.
  • Au besoin, diriger le travail des techniciens et former le personnel d’essais dans le cadre d’une validation.
  • Travailler de façon autonome pour planifier et organiser vos activités afin de respecter les échéanciers et communiquer en temps opportun.
  • Effectuer toute autre tâche requise.

Qualifications requises :

  • Baccalauréat en génie électrique (ou domaine connexe).
  • 3 ans ou plus d’expérience pertinente en développement de systèmes d’essais.
  • Compréhension des principes, concepts, outils et techniques d’ingénierie et de résolution de problèmes, ainsi que des notions fondamentales de gestion du changement et de validation des essais.
  • Capacité à développer des solutions créatives et à collaborer en tirant parti des idées des équipes multidisciplinaires. Défend ses idées avec passion tout en écoutant et en considérant celles des autres.
  • Initiative pour identifier les opportunités d’amélioration, les prioriser, les communiquer aux niveaux appropriés et les mener à terme.
  • Résilience face aux obstacles. Planifie adéquatement les risques et réagit positivement aux imprévus.
  • Excellentes compétences organisationnelles, en communication et en collaboration.
  • Solides compétences en documentation.

Qualifications souhaitées :

  • Expérience dans l’industrie des dispositifs médicaux (atout).
  • Conception d’équipements et de dispositifs de fixation, ainsi qu’expérience en développement de systèmes d’essais.
  • Développement de procédés, validations d’équipements et caractérisation des procédés.
  • Capacité à traduire des idées théoriques et abstraites en innovations concrètes.
  • Expérience en programmation LabVIEW et/ou C/C++.
  • Expérience avec SolidWorks.
  • Approche axée sur les données; expérience en analyse statistique.
  • Expérience en conception; développement de nouveaux produits.
  • Expérience en automatisation et avec les contrôleurs logiques programmables.

Maximum Salary: $113700

Compensation forhourly, non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forsalaried, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

Compensation for
sales rolesis governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives).

This job involves regular collaboration with colleagues, clients, and stakeholders across Canada, the U.S., and/or internationally, making proficiency in English essential for effective communication and alignment. English is necessary for engaging with a range of documentation and maintaining effective communication if interacting with external clients or vendors.

As detailed in the job description, this job involves communicating, both verbally and in writing, with other Boston Scientific teams located across Canada, the United States and/or with our international clients and partners. International customers and partners represent an important part of our activities. Based on an evaluation, we have determined that the duties of R&D Test Engineer II / Ingénieur d'essai R&D II position require knowledge of English in addition to French (oral and written). We also determined that the English language skills already required of other employees do not permit the performance of English language skills tasks related to R&D Test Engineer II / Ingénieur d'essai R&D II position.

However, in Québec, Boston Scientific limits as much as possible the number of positions for which it requires the knowledge of another language than French. Boston Scientific solely requires proficiency in English where it is necessary for the performance of an employee’s duties.

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21.11.2025
BS

Boston Scientific Senior Electrical Test Engineer / ingénieur Canada, Quebec, Montreal

Limitless High-tech career opportunities - Expoint
Analyze system requirements and electronic schematics to design and develop test plans and protocols to ensure designs meet requirements. Apply technical knowledge to innovate, design, and develop processes, procedures, fixturing,...
Description:

Additional Locations: Canada-QC-Montreal

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

About the Role
As a Senior R&D Electrical Test Engineer at Boston Scientific, you will play a key role in ensuring the performance and reliability of our medical devices. You will collaborate with cross-functional teams to design, develop, and execute comprehensive test plans, ensuring compliance with industry standards and regulations. Your contributions will have a direct impact on improving patient care by advancing innovative medical solutions.

Your Responsibilities Will Include:

  • Analyze system requirements and electronic schematics to design and develop test plans and protocols to ensure designs meet requirements.
  • Apply technical knowledge to innovate, design, and develop processes, procedures, fixturing, and/or automation.
  • Conduct engineering and design performance tests.
  • Analyze test results, detect issues, and track root causes.
  • Develop engineering and design verification test reports.
  • Work with a cross-functional team to address engineering challenges.
  • Provide work direction to technicians and train test personnel as part of validation when required.
  • Work independently to plan and schedule your activities to meet timelines and communicate progress effectively.
  • Perform additional duties as required.

Required Qualifications:

  • Bachelor’s or master’s degree in electrical engineering or related field.
  • 5-7 years of relevant experience in product development, particularly in test automation and fixture design.
  • Strong understanding of engineering and problem-solving principles, concepts, tools, and techniques.
  • Proficiency in test validation and change management processes.
  • Ability to develop creative solutions and collaborate with cross-functional teams, advocating for ideas while listening to and considering the team’s input.
  • Takes initiative to identify improvement opportunities, prioritize them, communicate them to appropriate levels, and follow through on their completion.
  • Excellent organizational, communication, and collaboration skills
  • Strong documentation skills.

Preferred Qualifications:

  • Experience in the medical device industry.
  • Experience in equipment and fixture design, as well as test systems development
  • Knowledge of process development, including equipment validations and process characterization.
  • Ability to translate theoretical and abstract ideas into innovative solutions.
  • Experience with LabVIEW and/or C/C++ programming.
  • Familiarity with SolidWorks.
  • Data-driven individual with statistical analysis experience.
  • Experience in new product development and design.
  • Experience with automation and programmable logic controllers

À propos du poste
En tant qu’ingénieur principal en essais électriques à la R. et D. chez Boston Scientific, le titulaire du poste joue un rôle clé en veillant à ce que nos dispositifs médicaux soient performants et fiables. Il collabore avec des équipes interfonctionnelles pour concevoir, développer et exécuter des plans d’essai détaillés, et ce, dans le respect des normes et de la réglementation en vigueur dans l’industrie. En contribuant au développement de solutions médicales novatrices, le titulaire du poste a une incidence directe sur l’amélioration des soins prodigués aux patients.

Responsabilités

  • Analyser les exigences des systèmes et les schémas électroniques afin de concevoir et d’élaborer des plans et des protocoles d’essai pour s’assurer que les concepts répondent aux exigences.
  • Appliquer des connaissances techniques pour innover ainsi que concevoir et développer des processus, des procédures, des montages ou des dispositifs d’automatisation.
  • Effectuer des essais de rendement en matière d’ingénierie et de conception.
  • Analyser les résultats des essais, détecter les problèmes et rechercher les causes profondes.
  • Rédiger des rapports d’essais de vérification en matière d’ingénierie et de conception.
  • Travailler avec une équipe interfonctionnelle pour résoudre les problèmes d’ingénierie.
  • Orienter le travail des techniciens et former le personnel chargé des essais dans le cadre du processus de validation, le cas échéant.
  • Travailler de manière autonome pour planifier et programmer ses activités afin de respecter les délais et produire de manière efficiente des rapports sur l’avancement des projets.
  • Effectuer d’autres tâches au besoin.

Compétences requises

  • Baccalauréat ou maîtrise en génie électrique ou dans un domaine connexe.
  • De 5 à 7 années d’expérience pertinente dans le développement de produits, en particulier dans le domaine de l’automatisation des essais et de la conception de dispositifs d’essai.
  • Excellente compréhension des principes, des concepts, des outils et des techniques d’ingénierie et de résolution de problèmes.
  • Maîtrise des processus de validation des essais et de gestion du changement.
  • Capacité à élaborer des solutions novatrices et à collaborer avec des équipes interfonctionnelles ainsi qu’à défendre ses idées tout en écoutant et en tenant compte des commentaires des autres membres de l’équipe.
  • Capacité à prendre l’initiative pour recenser les possibilités d’amélioration, à les classer par ordre de priorité, à les communiquer aux paliers hiérarchiques appropriés et à assurer le suivi de leur mise en œuvre.
  • Excellentes aptitudes en matière d’organisation, de communication et de collaboration.
  • Solides compétences en matière de documentation.

Compétences souhaitées

  • Expérience dans l’industrie des dispositifs médicaux.
  • Expérience dans la conception d’équipements et de dispositifs d’essai ainsi que dans le développement de systèmes d’essai.
  • Connaissance du développement des procédés, y compris la validation des équipements et la caractérisation des procédés.
  • Capacité à transformer des concepts théoriques et abstraits en des solutions novatrices.
  • Expérience en programmation sur LabVIEW ou C/C++.
  • Bonne connaissance de SolidWorks.
  • Personne intéressée par les données ayant de l’expérience en analyse statistique.
  • Expérience en matière de développement et de conception de nouveaux produits.
  • Expérience en automatisation et en contrôleurs logiques programmables.

Requisition ID: 616895

Minimum Salary: $79700

Maximum Salary: $158200

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see --will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for hourly, non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for salaried, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

Compensation for sales roles is governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives).

Our organization is across Canada and has commercial representation in 140 countries.

This job involves regular collaboration with colleagues, clients, and stakeholders across Canada, the U.S., and/or internationally, making proficiency in English essential for effective communication and alignment. English is necessary for engaging with a range of documentation and maintaining effective communication if interacting with external clients or vendors.

As detailed in the job description, this job involves communicating, both verbally and in writing, with other Boston Scientific teams located across Canada, the United States and/or with our international clients and partners. International customers and partners represent an important part of our activities. Based on an evaluation, we have determined that the duties of Senior Electrical Test Engineer / ingénieur principal en essais électriques position require knowledge of English in addition to French (oral and written). We also determined that the English language skills already required of other employees do not permit the performance of English language skills tasks related to Senior Electrical Test Engineer / ingénieur principal en essais électriques position.

However, in Québec, Boston Scientific limits as much as possible the number of positions for which it requires the knowledge of another language than French. Boston Scientific solely requires proficiency in English where it is necessary for the performance of an employee’s duties.

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

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21.11.2025
BS

Boston Scientific Senior R&D Test Engineer Cables / ingénieur principal en ess... Canada, Quebec, Montreal

Limitless High-tech career opportunities - Expoint
Analyzing system and design requirements to develop test plans, protocols, and reports that verify design compliance. Designing and conducting engineering, functional, and performance testing for electrical and electro-mechanical assemblies. Coordinating...
Description:

Additional Locations: Canada-QC-Montreal

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

About the role:

As a Senior R&D Test Engineer, you will be responsible for designing, executing, and improving test processes that ensure the safety, quality, and performance of Boston Scientific’s innovative medical technologies. Working within the Electrophysiology (EP) Capital Equipment division, you will plan and perform verification and validation activities for our cutting-edge medical devices, with a particular focus on cable assemblies and related hardware.

Your responsibilities will include:

  • Analyzing system and design requirements to develop test plans, protocols, and reports that verify design compliance.
  • Designing and conducting engineering, functional, and performance testing for electrical and electro-mechanical assemblies.
  • Coordinating test article shipments and tracking progress through sterilization, packaging, and mechanical reliability test flows.
  • Reviewing and approving test documentation to ensure accuracy, completeness, and consistency.
  • Supporting troubleshooting and failure investigations, compiling and analyzing test data to identify root causes and recommend improvements.
  • Developing and maintaining test fixtures, procedures, and automation tools to support testing efficiency.
  • Communicating with vendors and external partners regarding test scheduling, documentation, and equipment logistics.
  • Ensuring all activities comply with Boston Scientific’s Quality Policy and relevant regulatory requirements (FDA, ISO 13485).
  • Providing technical guidance and training to technicians or test personnel as required.
  • Planning and prioritizing individual work to meet deadlines and project milestones with minimal supervision.

Required qualifications:

  • Bachelor’s degree in electrical engineering or a related technical field.
  • 5+ years of experience in product or system development within a regulated industry.
  • Strong understanding of engineering and problem-solving principles, test validation, and change management.
  • Hands-on experience in developing and executing V&V tests for electrical or electro-mechanical systems.
  • Excellent documentation, organizational, and communication skills.
  • Demonstrated ability to work independently, manage multiple priorities, and drive tasks to completion.
  • Commitment to product quality and patient safety through rigorous testing and validation.

Preferred qualifications:

  • Experience in the medical device industry, with knowledge of FDA 21 CFR 820 and ISO 13485 requirements.
  • Experience in equipment and fixture design, test system development, and process validation.
  • Proficiency with LabVIEW and/or C/C++ programming for automated testing.
  • Experience using SolidWorks for designing test fixtures or mechanical components.
  • Familiarity with automation systems and programmable logic controllers (PLCs).
  • Experience performing data analysis or statistical evaluations using tools such as Minitab or JMP.
  • Exposure to new product development processes, particularly for capital equipment or electro-mechanical devices.

À propos du poste :

En tant qu’ingénieur principal en essais R&D, vous serez responsable de la conception, de l’exécution et de l’amélioration des processus d’essais afin d’assurer la sécurité, la qualité et la performance des technologies médicales novatrices de Boston Scientific. Au sein de la division des équipements capitaux en électrophysiologie (EP), vous planifierez et réaliserez des activités de vérification et de validation pour nos dispositifs médicaux de pointe, en mettant particulièrement l’accent sur les assemblages de câbles et les composants matériels connexes.

Vos responsabilités comprendront :

  • Analyser les exigences du système et de la conception afin d’élaborer des plans d’essais, des protocoles et des rapports permettant de vérifier la conformité de la conception.
  • Concevoir et exécuter des essais d’ingénierie, fonctionnels et de performance pour des assemblages électriques et électromécaniques.
  • Coordonner l’expédition des articles d’essais et assurer le suivi de leur progression à travers les étapes de stérilisation, d’emballage et d’essais de fiabilité mécanique.
  • Examiner et approuver la documentation d’essais afin d’en garantir l’exactitude, l’exhaustivité et la cohérence.
  • Soutenir les activités de dépannage et d’enquête sur les défaillances, en analysant les données d’essais pour identifier les causes fondamentales et recommander des améliorations.
  • Développer et entretenir les gabarits d’essai, les procédures et les outils d’automatisation afin d’optimiser l’efficacité des essais.
  • Communiquer avec les fournisseurs et partenaires externes concernant la planification des essais, la documentation et la logistique des équipements.
  • Veiller à ce que toutes les activités respectent la politique de qualité de Boston Scientific ainsi que les exigences réglementaires applicables (FDA, ISO 13485).
  • Fournir un encadrement technique et une formation au personnel technique ou aux techniciens, au besoin.
  • Planifier et prioriser les activités individuelles afin de respecter les échéanciers et les jalons de projet avec un minimum de supervision.

Qualifications requises :

  • Baccalauréat en génie électrique ou dans un domaine technique connexe.
  • Plus de 6 ans d’expérience en développement de produits ou de systèmes dans une industrie réglementée.
  • Solide compréhension des principes d’ingénierie, de résolution de problèmes, de validation d’essais et de gestion du changement.
  • Expérience pratique dans la conception et l’exécution d’essais de vérification et de validation pour des systèmes électriques ou électromécaniques.
  • Excellentes compétences en documentation, en organisation et en communication.
  • Capacité démontrée à travailler de façon autonome, à gérer plusieurs priorités et à mener les tâches à terme.
  • Engagement envers la qualité des produits et la sécurité des patients grâce à une validation et des essais rigoureux.

Qualifications préférées :

  • Expérience dans l’industrie des dispositifs médicaux, avec une connaissance des exigences de conformité FDA 21 CFR 820 et ISO 13485.
  • Expérience en conception d’équipements et de gabarits, en développement de systèmes d’essais et en validation de procédés.
  • Maîtrise de LabVIEW et/ou de la programmation C/C++ pour les essais automatisés.
  • Expérience avec SolidWorks pour la conception de gabarits d’essais ou de composants mécaniques.
  • Connaissance des systèmes d’automatisation et des automates programmables industriels (API/PLC).
  • Expérience en analyse de données ou en évaluations statistiques à l’aide d’outils tels que Minitab ou JMP.
  • Exposition aux processus de développement de nouveaux produits, particulièrement dans le domaine des équipements capitaux ou des systèmes électromécaniques.

Requisition ID: 615989

Minimum Salary: $79700

Maximum Salary: $158200

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see --will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for hourly, non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for salaried, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

Compensation for sales roles is governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives).

Our organization is across Canada and has commercial representation in 140 countries.

This job involves regular collaboration with colleagues, clients, and stakeholders across Canada, the U.S., and/or internationally, making proficiency in English essential for effective communication and alignment. English is necessary for engaging with a range of documentation and maintaining effective communication if interacting with external clients or vendors.

As detailed in the job description, this job involves communicating, both verbally and in writing, with other Boston Scientific teams located across Canada, the United States and/or with our international clients and partners. International customers and partners represent an important part of our activities. Based on an evaluation, we have determined that the duties of Senior R&D Test Engineer (Cables) / ingénieur principal en essais R&D (câbles) position require knowledge of English in addition to French (oral and written). We also determined that the English language skills already required of other employees do not permit the performance of English language skills tasks related to Senior R&D Test Engineer (Cables) / ingénieur principal en essais R&D (câbles) position.

However, in Québec, Boston Scientific limits as much as possible the number of positions for which it requires the knowledge of another language than French. Boston Scientific solely requires proficiency in English where it is necessary for the performance of an employee’s duties.

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

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20.09.2025
BS

Boston Scientific R&D Systems Engineering Manager / Gestionnaire Canada, Quebec, Montreal

Limitless High-tech career opportunities - Expoint
Develop the system engineering discipline cross functionally through focus on system architecture, interfaces, and defining sub-systems. Oversee and drive the system development lifecycle, from design and development to testing, deployment,...
Description:

About the role

The R&D Systems Engineering Manager will provide leadership, vision, and direction within the EP Capital Equipment Systems. In the role of an R&D Manager, you will be responsible for supporting the growth and continued development of the Systems Engineering team and function; overseeing technical staff members and helping to define and foster functional excellence. You will have the opportunity to significantly impact the development of truly life changing patient therapies for the relief of debilitating diseases.

Your responsibilities will include:

  • Develop the system engineering discipline cross functionally through focus on system architecture, interfaces, and defining sub-systems.
  • Oversee and drive the system development lifecycle, from design and development to testing, deployment, maintenance, and security for capital equipment.
  • Lead a team of system engineers including recruiting, hiring, mentoring, professional development, and performance coaching.
  • Oversee requirements development and requirements management tool development.
  • Build strong collaboration with development sites and cross-functional partners.
  • Cultivate a culture of continuous improvement by staying informed about industry trends, technological advancements, and emerging tools in medical device systems engineering, design controls, and testing.
  • Monitor and ensure compliance with company policies and procedures.
  • Providing input for submissions to regulatory bodies and governmental agencies.

Required qualifications:

  • Bachelor of Science degree in a relevant engineering discipline
  • 8+ years’ experience managing technical teams in the development of a similarly complex system
  • Demonstrated expertise in systems engineering for the design, development and testing of medical devices
  • Ability to lead a multi-site team and collaborate with peers in different locations
  • Experience working with requirement management, collaboration, and issue tracking tools such as Jama and Jira
  • Working knowledge of hardware, firmware, and software evaluation to standards such as IEC 62304 and ISO 60601

Preferred qualifications:

  • Successful history of launching and maintaining products within the medical device industry
  • Ability to direct and control the activities, budget, and headcount for the department

À propos du poste

Le gestionnaire R et D en ingénierie des systèmes a pour fonction d’assurer le leadership au sein de l’équipe des Systèmes de biens d’équipement d’électrophysiologie ainsi que d’établir la vision de cette équipe et de définir les orientations à suivre. En tant que gestionnaire R et D, le titulaire du poste est responsable du soutien de la croissance et du développement continu de l’équipe et de la fonction d’ingénierie des systèmes, de la supervision des membres du personnel technique ainsi que de la définition et de la promotion de l’excellence fonctionnelle. Il aura l’occasion d’exercer une influence considérable sur le développement de traitements qui changent véritablement la vie des patients et soulagent ceux atteints de maladies invalidantes.

Vos responsabilités comprendront :

  • Développer la discipline de l’ingénierie des systèmes de manière transversale en mettant l’accent sur l’architecture des systèmes, les interfaces et la définition des sous-systèmes.
  • Superviser et piloter le cycle de vie du développement des systèmes, de la conception et du développement aux tests, en passant par le déploiement, la maintenance et la sécurité des équipements.
  • Diriger une équipe d’ingénieurs en systèmes, notamment en ce qui concerne le recrutement, l’embauche, le mentorat, le perfectionnement professionnel et l’accompagnement sur le plan des résultats.
  • Superviser la définition des exigences et la mise au point d’outils de gestion des exigences.
  • Établir une collaboration solide avec les sites de développement et les partenaires interfonctionnels.
  • Entretenir une culture d’amélioration continue en se tenant informé des tendances du secteur, des avancées technologiques et des nouveaux outils en matière d’ingénierie des systèmes de dispositifs médicaux, de contrôle de la conception et de tests.
  • Fournir des commentaires pour les soumissions aux organismes de réglementation et aux agences gouvernementales.
  • Surveiller et assurer la conformité aux politiques et procédures de l’entreprise.

Qualifications requises:

  • Baccalauréat en sciences dans une discipline d’ingénierie pertinente
  • Plus de 8 ans d’expérience dans la gestion d’équipes techniques pour le développement d’un système de complexité similaire
  • Expertise démontrée en ingénierie des systèmes pour la conception, le développement et la mise à l’essai de dispositifs médicaux
  • Capacité à diriger une équipe répartie sur plusieurs sites et à collaborer avec des collègues situés à différents endroits
  • Expérience avec des outils de gestion des exigences, de collaboration et de suivi des problèmes tels que Jama et Jira
  • Connaissance pratique de l’évaluation du matériel, du micrologiciel et du logiciel selon des normes telles que l’IEC 62304 et l’ISO 60601

Qualifications souhaitées:

  • Expérience avérée dans le lancement et le maintien de produits au sein de l’industrie des dispositifs médicaux
  • Capacité à diriger et à contrôler les activités, le budget et l’effectif du service

Maximum Salary: $189800

Compensation forhourly, non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forsalaried, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

Compensation for
sales rolesis governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives).

This job involves regular collaboration with colleagues, clients, and stakeholders across Canada, the U.S., and/or internationally, making proficiency in English essential for effective communication and alignment. English is necessary for engaging with a range of documentation and maintaining effective communication if interacting with external clients or vendors.

As detailed in the job description, this job involves communicating, both verbally and in writing, with other Boston Scientific teams located across Canada, the United States and/or with our international clients and partners. International customers and partners represent an important part of our activities. Based on an evaluation, we have determined that the duties of R&D Systems Engineering Manager / Gestionnaire R et D en ingénierie des systèmes position require knowledge of English in addition to French (oral and written). We also determined that the English language skills already required of other employees do not permit the performance of English language skills tasks related to R&D Systems Engineering Manager / Gestionnaire R et D en ingénierie des systèmes position.

However, in Québec, Boston Scientific limits as much as possible the number of positions for which it requires the knowledge of another language than French. Boston Scientific solely requires proficiency in English where it is necessary for the performance of an employee’s duties.

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19.09.2025
BS

Boston Scientific Design Quality Intern / Stagiaire en qualité de conception Canada, Quebec, Montreal

Limitless High-tech career opportunities - Expoint
Work in cross-functional teams to support and execute processes and quality deliverables associated with projects and quality systems. Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality...
Description:

Please note this is a 6-month internship opportunity beginning in October 2025.


Your responsibilities will include:

  • Work in cross-functional teams to support and execute processes and quality deliverables associated with projects and quality systems.
  • Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
  • Proactively investigate, identify, and implement best-in-class quality practices.
  • Builds quality into all aspects of work by maintaining compliance to all quality requirements.
  • Knowledgeable on Risk Management.
  • Ensure completion of assigned project deliverables per set schedules.
  • Maintain cross-functional team relationship; collaborate effectively and positively with peers.

Required qualifications:

  • Bachelor’s or master’s degree in electrical or biomedical engineering.
  • 0 - 1 years of experience in the medical device industry.
  • Strong problem-solving skills in a team environment.
  • Excellent organizational, communication and collaboration skills.
  • Strong documentation skills.

Preferred qualifications:

  • Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources.
  • Excellent organizational, communication and collaboration skills.
  • Ability to work with a team efficiently and independently.

Veuillez noter qu’il s’agit d’un stage d’une durée de 6 mois débutant en Octobre 2025.

Vos responsabilités comprendront :

  • Travailler au sein d’équipes multidisciplinaires pour appuyer et exécuter les processus et les livrables de qualité liés aux projets et aux systèmes de qualité.
  • Appliquer des méthodes rigoureuses et systématiques de résolution de problèmes pour identifier, prioriser, communiquer et résoudre les enjeux de qualité.
  • Enquêter de façon proactive, identifier et mettre en œuvre les meilleures pratiques en matière de qualité.
  • Intégrer la qualité dans tous les aspects du travail en respectant l’ensemble des exigences réglementaires et normatives.
  • Avoir de bonnes connaissances en gestion des risques.
  • Assurer la réalisation des livrables de projet assignés selon les échéanciers établis.
  • Maintenir de bonnes relations interfonctionnelles ; collaborer efficacement et positivement avec ses collègues.

Qualifications requises:

  • Baccalauréat ou maîtrise en génie électrique ou biomédical.
  • De 0 à 1 an d’expérience dans l’industrie des dispositifs médicaux.
  • Solides compétences en résolution de problèmes dans un environnement de travail en équipe.
  • Excellentes aptitudes en organisation, communication et collaboration.
  • Solides compétences en rédaction et en tenue de documentation.

Qualifications souhaitées:

  • Capacité à tirer des conclusions et à formuler des recommandations à partir de données techniques provenant de sources multiples et variées.
  • Excellentes aptitudes en organisation, communication et collaboration.
  • Capacité à travailler efficacement en équipe ainsi que de manière autonome.

Maximum Salary: $56800

Compensation forhourly, non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forsalaried, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

Compensation for
sales rolesis governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives).

This job involves regular collaboration with colleagues, clients, and stakeholders across Canada, the U.S., and/or internationally, making proficiency in English essential for effective communication and alignment. English is necessary for engaging with a range of documentation and maintaining effective communication if interacting with external clients or vendors.

As detailed in the job description, this job involves communicating, both verbally and in writing, with other Boston Scientific teams located across Canada, the United States and/or with our international clients and partners. International customers and partners represent an important part of our activities. Based on an evaluation, we have determined that the duties of Design Quality Intern / Stagiaire en qualité de conception position require knowledge of English in addition to French (oral and written). We also determined that the English language skills already required of other employees do not permit the performance of English language skills tasks related to Design Quality Intern / Stagiaire en qualité de conception position.

However, in Québec, Boston Scientific limits as much as possible the number of positions for which it requires the knowledge of another language than French. Boston Scientific solely requires proficiency in English where it is necessary for the performance of an employee’s duties.

Show more

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Limitless High-tech career opportunities - Expoint
Wsparcie działań GBS i Payroll w zadaniach administracyjnych w regionie EMEA. Utrzymywanie i aktualizacja treści wewnętrznych (np. FAQ) na portalu firmowym. Przygotowywanie i dostarczanie raportów zespołom wewnętrznym i interesariuszom. Organizowanie...
Description:

Opis stanowiska:

Poszukujemy Stażysty ds. Wsparcia Administracyjnego, który dołączy do naszych zespołów Payroll oraz Global Business Services (GBS), wspierając działania w krajach regionu EMEA. To idealna rola dla osoby, która lubi pracować z danymi, systemami i różnymi działami, zapewniając płynność procesów biznesowych. Będziesz zajmować się koordynacją informacji, dbaniem o spójność danych oraz wspieraniem narzędzi cyfrowych usprawniających pracę organizacji.

Twoje obowiązki:

· Wsparcie działań GBS i Payroll w zadaniach administracyjnych w regionie EMEA.

· Utrzymywanie i aktualizacja treści wewnętrznych (np. FAQ) na portalu firmowym.

· Przygotowywanie i dostarczanie raportów zespołom wewnętrznym i interesariuszom.

· Organizowanie i uzgadnianie danych na potrzeby raportowania i operacji.

· Weryfikacja i kontrola danych pracowników w systemach.

· Wsparcie testów i dokumentacji w ramach inicjatyw automatyzacji procesów.

Szukamy osoby, która:

· Jest w trakcie studiów licencjackich lub ukończyła kierunek administracja, języki lub pokrewne.

· Biegle posługuje się językiem angielskim i niemieckim (min. B2+). Znajomość innych języków będzie atutem.

· Posiada silne umiejętności organizacyjne i administracyjne.

· Dobrze zna pakiet Microsoft Office i szybko uczy się nowych systemów.

· Jest skrupulatna, analityczna i potrafi rozwiązywać problemy.

· Potrafi pracować samodzielnie oraz w zróżnicowanym, międzynarodowym środowisku.

· Dobrze zarządza czasem i priorytetami.

Oferujemy:

· Umowę stażową do 12 miesięcy, elastyczne godziny (30–40 godz./tyg.).

· Model hybrydowy (3 dni w biurze).

· Międzynarodowe środowisko pracy i wspierających współpracowników.

· Możliwość rozwoju umiejętności administracyjnych i koordynacyjnych w globalnej organizacji.

· Nowoczesne biuro w centrum Warszawy.

Lokalizacja: Warszawa (Hybrydowo)

Start: Grudzień/Styczeń 2025

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