Manufacturing Sr Engineer

2 months ago

Montreal, Canada Zimmer Biomet Full time
Chez Zimmer Biomet, nous croyons qu'il faut repousser les limites de l'innovation et faire avancer notre mission. En tant que leader mondial de la technologie médicale depuis près de 100 ans, la mobilité d'un patient est améliorée par un produit ou une technologie Zimmer Biomet toutes les 8 secondes.

En tant que membre de l'équipe Zimmer Biomet, vous partagerez notre engagement à offrir une mobilité et une vie renouvelée aux personnes du monde entier. Pour soutenir notre équipe talentueuse, nous nous concentrons sur les opportunités de développement, des groupes de ressources pour les employés (ERG) solides, un environnement de travail flexible, des récompenses globales compétitives spécifiques à l'emplacement, des incitations au bien-être et une culture de reconnaissance et de récompenses de performance. Nous nous engageons à créer un environnement dans lequel chaque membre de l'équipe se sent inspiré, investi, pris en charge, valorisé et possède un fort sentiment d'appartenance.

At Zimmer Biomet, we believe in pushing the boundaries of innovation and advancing our mission. As a global leader in medical technology for nearly 100 years, a Zimmer Biomet product or technology enhances a patient's mobility every 8 seconds.

As a member of the Zimmer Biomet team, you will share our commitment to providing renewed mobility and life to people around the world. To support our talented team, we focus on development opportunities, strong employee resource groups (ERGs), a flexible work environment, competitive location-specific rewards, wellness incentives, and a culture of recognition and performance rewards. We are dedicated to creating an environment where every team member feels inspired, invested, supported, valued, and has a strong sense of belonging.

Ce qu'on vous propose

Sous la supervision du responsable ingénierie de production, vous travaillerez en partenariat avec les équipes de conception afin de transférer les designs des nouveaux produits chez les différents fournisseurs. Votre rôle consistera à participer aux revues de design à l'interne, travailler avec les designers pour favoriser la fabrication efficace des produits, s'assurer que les fournisseurs respectent nos requis qualités liés à la production tel que la validation des procédés critiques (IQ, OQ, PQ), travailler à la gestion des risques de production (PFMEA) et à la validation des méthodes d'inspection (TMV, Gage R&R). Vous serez également responsable d'assurer l'efficacité et la qualité de la production des produits déjà existants chez les fournisseurs.

Comment vous aurez un impact

  • Prendre en charge le transfert des nouveaux produits vers la production chez les fournisseurs.
  • Responsable du choix des fournisseurs et du transfert de production d'un fournisseur vers un autre.
  • Visiter régulièrement les principaux fournisseurs de manière à favoriser la recherche de solutions, le transfert de production, le suivi de production ainsi que s'assurer que les requis qualités sont bien suivis (Canada, USA, Europe).
  • Responsable des méthodes d'inspections et de leur validation (gage R&R) chez les fournisseurs et à notre département de métrologie.
  • Participer étroitement à la validation (IQ, OQ, PQ) des différents procédés des nouvelles chaines d'approvisionnement chez les fournisseurs et à l'interne.
  • S'assurer que les fournisseurs appliquent une méthode efficace de gestion des risques de production (PFMEA).
  • Participer à l'amélioration continue de la gamme de produits déjà existant en prenant charge la modification des spécifications et en étant responsable de la partie production de la documentation liée à ces changements.
  • Servir d'interface entre fournisseurs, gestionnaire de projet, responsable des achats, groupe qualité et le groupe de conception.
  • Travailler étroitement avec les autres ingénieurs manufacturiers de la compagnie de manière à améliorer la pratique commune.
  • Participer à la définition et à l'amélioration continue des procédures et instructions de travail reliées à la production.
  • Participer aux revues de design avec le groupe de développement de produits et proposer des méthodes de fabrication et d'inspection efficaces.
  • Responsable de l'exécution du plan de maintenance et du suivi des équipements à l'interne.
  • Exécuter les analyses nécessaires au traitement des pièces non-conformes et des plaintes clients ainsi que mettre en place des solutions pour en éliminer les causes.


Ce qui vous fera remarquer

  • Vous avez démontré travailler efficacement avec des fournisseurs de matériels et de services.
  • Vous êtes parfaitement bilingue (français et anglais, écrit et oral).
  • Vous êtes une personne minutieuse dotée d'un bon esprit de synthèse capable de produire des rapports, documents et protocoles précis, concis et exacts.
  • Vous êtes reconnue pour vos excellentes habilités de communication.
  • Vous êtes doté d'une très bonne capacité à travailler en équipe multidisciplinaire.
  • Vous êtes une personne organisée dotée d'une aisance à gérer efficacement plusieurs tâches en parallèle.


Votre parcours

  • Vous êtes ingénieur mécanique, électrique, manufacturier ou industriel.
  • Vous possédez 3 à 10 ans d'expérience en lien avec des contraintes et requis de production (Domaine médical constitue un atout).
  • Vous possédez de l'expérience de travail dans un environnement ISO9001 et/ou ISO13485.
  • Vous possédez de l'expérience en fabrication de dispositifs électroniques.
  • Vous possédez de l'expérience en emballage de produits stériles.
  • Vous possédez une bonne connaissance des procédés d'usinage de métal (injection plastique), un aout.
  • Vous possédez de l'expérience avec plusieurs procédés de fabrication. (soudure, traitement thermique, passivation, etc.), un atout.


Déplacements

  • Jusqu'à 25%
  • Un passeport à jour est requis


What You Can Expect

Under the supervision of the manager, the candidate would work in collaboration with the design and development teams to transfer the design of new products to different suppliers. Their role consists of participating in internal design reviews, working with designers to ensure ease of manufacturability of the products, ensuring that the suppliers follow ZimmerCAS's quality requirements related to production and manufacturing, such as the validation of Special Processes (IQ, OQ, PQ), ensuring proper means of risk management during production (pFMEA) and validating the inspection methods (TMV, Gage R&R). The candidate will equally be responsible for maintaining the efficiency and quality of the production of existing parts being fabricated at the suppliers.

How You'll Create Impact

  • Leading the production transfer of new products to the suppliers' sites.
  • Participating in the supplier selection process and leading the production transfer from supplier site to supplier site.
  • Visiting suppliers onsite to facilitate finding solutions to manufacturing issues, performing production transfer activities, following up on production progress and ensuring that quality objectives are met during production (Canada, USA and Europe).
  • Developing inspection methods with the supplier and validating said methods (Gage R&R) both at the supplier site and internally at ZimmerCAS.
  • Ensuring the supplier applies the proper and effective risk management method for production (pFMEA).
  • Participating in the continuous improvement on the existing products by taking charge of spec modifications and drafting any documents related to these spec modifications.
  • Serving as the point of contact between the suppliers, project manager, sourcing representative, Quality team and the design and development team.
  • Collaborating with the other manufacturing engineers to improve common processes.
  • Participating in defining and continuously improving internal procedures and work instructions related to production activities.
  • Participating in design reviews with the design group and proposing effective manufacturing methods and inspection methods.
  • Executing the maintenance plan for the equipment used internally.
  • Analyzing part non-conformities and customer complaints, and implementing solutions to eliminate the root causes.


What Makes You Stand Out

  • Good working experience with suppliers providing goods and/or services.
  • Excellent oral and written communication skills in both French and English.
  • Detail-oriented and meticulous with drafting documentation, and a capability to produce clear and concise reports, documents and protocols;
  • Team player with the ability to work with multiple cross-functional teams;
  • Strong sense of ownership and organization skills with the capability of managing multiple tasks and projects concurrently;
  • You are an organized person with the ability to effectively manage multiple tasks in parallel.


Your Background

  • A degree in the field of engineering (mechanical, electrical, manufacturing or industrial).
  • 3 to 10 years of experience in a manufacturing environment (ideally in the Medical Device domain).
  • Experience working in a highly regulated environment under ISO 13485 or ISO 9001.
  • Experience in the production of electronic devices.
  • Experience working with sterile packaging.
  • Good working knowledge of the machining of metal instruments and plastic injection molding, an asset.
  • Experience in multiple manufacturing processes (welding, heat treatment, passivation, etc.), an asset.


Travel Expectations

  • Up to 25%
  • A current passport is required


Zimmer Biomet encourage les femmes, les personnes issues de minorités visibles, autochtones ou en situation de handicap à soumettre leur candidature.

Zimmer Biomet encourages women, people from visible minorities, aboriginals or people with disabilities to apply.

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