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Mechanical Assoc Engineer II

$65k - $80k per year
Full-time

Zimmer Biomet

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

Sous la supervision du Chef, Ingénierie mécanique, vous travaillerez au développement et à l’amélioration d’instruments de chirurgie assistée par ordinateur. Vous serez responsable de livrer des designs innovants et de qualité, dans les délais prescrits et selon les normes en vigueur.

Under the supervision of the Chief, Mechanical Engineering, you will work on the development and improvement of computer-assisted surgical instruments. You will be responsible for delivering innovative and quality designs, within the prescribed deadlines and according to current standards.

How You'll Create Impact

  • Concevoir et améliorer des instruments chirurgicaux réutilisables et jetables, ainsi que toute composante physique nécessaire à leur livraison (emballages, étiquettes, …). Plus précisément, participer à la recherche de solutions, concevoir les modèles 3D sur logiciel CAD.
  • Faire produire et tester les prototypes, déterminer les procédés de fabrication, réaliser les dessins de fabrication et participer activement au transfert du design vers la production dans un contexte de fabrication en sous[1]traitance.
  • Participer activement à des laboratoires et rencontres avec les chirurgiens collaborateurs pour obtenir le feedback sur les prototypes en cours de développement.
  • Réaliser des analyses (modes de défaillances, dimensionelles, fonctionelles, de résistance et autres) nécessaire à la relâche des produits.
  • Rédiger l’ensemble de la documentation qualité nécessaire à la mise en marché des produits (analyse de risque, requis de conception et autres).
  • Mettre en place des protocoles de tests (vérification de design) utilisant des méthodes scientifiquement validées et utilisant des méthodes statistiques valides.
  • Participer à la résolution de plaintes clients et des produits non-conformes en faisant l’analyse du problème, en trouvant les causes, en revoyant les risques associés et en proposant une solution.
  • Participer à la définition et à l’amélioration continue des procédures et instructions de travail reliées à la conception mécanique et à la production à l’intérieur du système qualité de la compagnie.
  • Faire l’estimation, la planification et la gestion des projets dans un environnement agile (Scrum, Kanban, …) en interagissant avec les différents groupes fonctionnels.
  • Design and improve reusable and disposable surgical instruments, as well as any physical components necessary for their delivery (packaging, labels, ...). More precisely, participate in the search for solutions, design 3D models on CAD software.
  • Have prototypes produced and tested, determine manufacturing processes, produce production drawings, and actively participate in the transfer from design to production in a subcontracting manufacturing context.
  • Actively participate in laboratories and meetings with collaborating surgeons to obtain feedback on the prototypes under development.
  • Perform analyses (failure modes, dimensions, functions, resistance and others) necessary for the release of products.
  • Write all the quality documentation necessary for the marketing of products (risk analysis, design requirements and others).
  • Implement testing protocols (design verification) using scientifically validated methods and using valid statistical methods.
  • Participate in the resolution of customer complaints and non-compliant products by analyzing the problem, finding the causes, reviewing the associated risks, and proposing a solution.
  • Participate in the definition and continuous improvement of procedures and work instructions related to mechanical design and production within the company’s quality system.
  • Estimate, plan and manage projects in an agile environment (Scrum, Kanban, etc.) by interacting with the various functional groups.

What Makes You Stand Out

  • Vous êtes disponible et intéressé à effectuer des voyages occasionnels.
  • Vous possédez une bonne connaissance des procédés d’usinage de métal et d’assemblage mécano-soudé.
  • Vous possédez de bonnes aptitudes de design d’outils en fonction des contraintes de performance et de fonctionnalité.
  • Vous possédez la passion de solutionner des problèmes complexes.
  • Vous travaillez efficacement avec des fournisseurs de matériels et de services.
  • Vous possédez de l’expérience de travail dans un environnement ISO13485.
  • Vous êtes une personne d’initiatives capable de gérer efficacement plusieurs tâches en parallèles tout en respectant les priorités et échéanciers.
  • Vous êtes doté d’une très bonne capacité à travailler en équipe multidisciplinaire.
  • Vous êtes une personne minutieuse dotée d’un bon esprit de synthèse capable de produire des rapports, documents et protocoles précis, concis et exact.
  • Vous êtes reconnu pour vos excellentes habiletés de communication
  • Vous avez un grand intérêt pour le domaine orthopédique et l’amélioration de la qualité de vie des gens
  • You are available and interested in making occasional trips.
  • You have a good knowledge of metal machining and welded assembly processes.
  • You have good tool design skills based on performance and functionality constraints.
  • You have a passion for solving complex problems.
  • You work effectively with suppliers of equipment and services.
  • You have experience working in an ISO13485 environment.
  • You are a person of initiatives able to effectively manage several tasks in parallel while respecting priorities and deadlines.
  • You have a very good ability to work in a multidisciplinary team.
  • You are a meticulous person with a good sense of synthesis capable of producing reports, documents and protocols that are precise, concise and accurate.
  • You are recognized for your excellent communication skills.
  • You have a great interest in the orthopedic field and in improving people’s quality of life.

Your Background

  • You are a mechanical engineer and have experience in mechanical design in a highly regulated industry (aeronautics, biomedical, etc.);
  • You are bilingual (French and English, written and spoken).
  • You have acquired a solid experience in CAD (SolidWorks is an asset).
  • Vous êtes ingénieur mécanique et avez de l’expérience en conception mécanique dans une industrie hautement règlementée (aéronautique, biomédical, etc.);
  • Vous êtes bilingue (français et anglais, écrit et oral).
  • Vous avez acquis une expérience solide en CAD (SolidWorks constitue un atout).

Physical Requirements

Travel Expectations

Up to 15% travel

Salary Expectations

$65,000 - $80,000 CAN

EOE/M/F/Vet/Disability

Vacancy posted 7 days ago
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