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    Systems Sr Designer - Toronto, Canada - Zimmer Biomet

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    Description
    JOB DESCRIPTION

    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 recognized.

    What You Can Expect

    Qu'est que vous pouvez attendre de ce role.

    Dans ce rôle, le candidat travaillera en tant qu'ingénieur en conception de systèmes, au sein d'une équipe multidisciplinaire, dont la principale responsabilité est de participer au développement de produits hautement innovants basé sur la Réalité Mixte et conçus pour les chirurgiens orthopédiques, soutenir le déploiement sur le marché et maintenir les applications existantes

    Nous cherchons un candidat ayant de l'expérience dans le développement de produits répondant à des normes de qualité et réglementaires strictes ainsi qu'une expérience dans ces différentes phases d'un projet : conceptualisation, développement, tests, mise en service et commercialisation.

    Dans un environnement agile, il sera responsable des éléments suivants : identification des obstacles, participation à Agile Tour ou équivalent, capacité à agir en tant que représentant du Product Owner Proxi ou Scrum Master, et promotion des changements pour une amélioration continue.

    How You'll Create Impact

    Comment créer de l'impact

    Analyser les différents besoins (utilisateur, entreprise, réglementaire, etc.) et définir les spécifications du système, tout en tenant compte des exigences techniques et fonctionnelles;

    Identifier, évaluer et analyser les risques liés au produit;

    Participer à la vérification et à la validation du produit;

    Participer aux tests d'utilisabilité avec les clients;

    Gérer la traçabilité des exigences;

    Rédiger les documents qualité liés à la conception et au développement du produit dans le respect des normes et procédures applicables pour assurer la qualité et la sécurité du produit;

    Travailler dans un environnement Agile et Scrum;

    Interagir avec différentes équipes pour explorer de nouvelles technologies afin d'obtenir une fiabilité et une qualité de produit supérieures aux normes, permettant à l'entreprise de maintenir sa position de leader dans l'industrie.

    What Makes You Stand Out

    Qu'est-ce qui vous fera remarquer.

    Capacité à gérer efficacement les priorités et les échéanciers;

    Capacité à travailler de manière autonome et efficace au sein d'une équipe;

    Capacité à gérer la pression et à travailler dans l'ambiguïté, à obtenir un consensus, à gérer plusieurs priorités et à identifier des solutions créatives à des problèmes complexes;

    Solides capacités d'analyse et de jugement;

    Solide expérience dans l'identification et l'analyse des risques associés aux produits;

    Haut niveau de responsabilité personnelle et d'intégrité;

    Excellentes compétences en communication écrite et verbale en français et en anglais.

    Your Background

    Votre parcours.

    Baccalauréat en génie ou en sciences dans un domaine connexe (informatique, génie logiciel, biomédical ou équivalent).

    3 à 5 années d'expérience en développement de produits R&D, idéalement dans un domaine hautement réglementé (médical, aéronautique ou pharmaceutique).

    Atouts

    Product Owner, ou Scrum Master;

    Spécialiste de la vérification/validation de logiciels;

    Expérience avec des équipes de développement Agile/Scrum et avec Confluence et Jira ;

    Connaissance des réglementations de medical design regulations (e.x. 21 CFR 820, ISO13485, ISO14971, IEC62304, IEC62366, etc).

    Travel Expectations

    Voyagement

    Jusqu'à 5%.

    Un passeport à jour est requis.

    EOE/M/F/Vet/Disability



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