Job Description

Additional Locations: Canada-QC-MontrealDiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt 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.\xc3\x80 propos du posteBoston Scientific vous propose une culture ax\xc3\xa9e sur la collaboration et anim\xc3\xa9e par une passion pour l\'innovation qui fait en sorte que nous sommes toujours en interaction au niveau le plus essentiel. Avec d\xc3\xa9termination et imagination ainsi qu\'avec un souci profond de la vie humaine, nous r\xc3\xa9solvons certains des d\xc3\xa9fis les plus importants de l\'industrie des soins de sant\xc3\xa9. Ensemble, nous formons une \xc3\xa9quipe internationale dont l\'objectif est d\'am\xc3\xa9liorer la vie des gens partout dans le monde. Ici, vous pouvez avoir une carri\xc3\xa8re qui a du sens - am\xc3\xa9liorer des vies gr\xc3\xa2ce au travail de votre vie. Nous sommes \xc3\xa0 la recherche d\'un directeur de projet pour les syst\xc3\xa8mes de R. et D. poss\xc3\xa9dant de solides connaissances en la mati\xc3\xa8re et capable d\'appliquer des concepts, des proc\xc3\xa9dures et des pratiques techniques et commerciales dans le domaine de l\'ing\xc3\xa9nierie de projet. Nous voulons une personne capable d\'interpr\xc3\xa9ter les politiques et les proc\xc3\xa9dures de l\'entreprise pour r\xc3\xa9soudre les probl\xc3\xa8mes li\xc3\xa9s aux applications biom\xc3\xa9dicales. Nous d\xc3\xa9sirons recruter une personne ayant une bonne connaissance de la gestion du cycle de vie du d\xc3\xa9veloppement des produits.Responsabilit\xc3\xa9s

• Participer \xc3\xa0 la planification, \xc3\xa0 l\'ex\xc3\xa9cution et \xc3\xa0 la finalisation des projets, tout en respectant des d\xc3\xa9lais stricts et le budget imparti et en suivant des proc\xc3\xa9dures organis\xc3\xa9es et reproductibles.
• Participer \xc3\xa0 l\'\xc3\xa9laboration et \xc3\xa0 la mise \xc3\xa0 jour des calendriers des projets.
• Coordonner les efforts des membres de l\'\xc3\xa9quipe et des sous-traitants ou d\'experts-conseils externes afin de faire en sorte que les projets puissent \xc3\xaatre r\xc3\xa9alis\xc3\xa9s conform\xc3\xa9ment au plan \xc3\xa9tabli.
• Assurer la liaison avec les parties concern\xc3\xa9es par le projet et communiquer efficacement les attentes du projet aux membres de l\'\xc3\xa9quipe et aux autres parties concern\xc3\xa9es en temps opportun et de mani\xc3\xa8re claire.
• Recenser et g\xc3\xa9rer les contraintes et les \xc3\xa9l\xc3\xa9ments critiques de la r\xc3\xa9alisation des projets, tout en assurant la qualit\xc3\xa9 des produits et en utilisant et en suivant les m\xc3\xa9thodologies appropri\xc3\xa9es.
• Effectuer des analyses r\xc3\xa9trospectives des projets et en communiquer les conclusions afin de mettre en \xc3\xa9vidence les r\xc3\xa9ussites et les lacunes observ\xc3\xa9es.
• Faire preuve en tout temps d\'un engagement inconditionnel envers la s\xc3\xa9curit\xc3\xa9 des patients et de la qualit\xc3\xa9 des produits en respectant la politique d\'assurance de la qualit\xc3\xa9 et tous les autres processus et proc\xc3\xa9dures document\xc3\xa9s \xc3\xa0 cet \xc3\xa9gard.
• Effectuer d\'autres t\xc3\xa2ches le cas \xc3\xa9ch\xc3\xa9ant.

Qualifications requises

• Baccalaur\xc3\xa9at en g\xc3\xa9nie, ma\xc3\xaetrise dans le domaine biom\xc3\xa9dical ou dans un domaine connexe.
• Au moins quatre ann\xc3\xa9es d\'exp\xc3\xa9rience dans le domaine du d\xc3\xa9veloppement de produits au sein d\'un secteur r\xc3\xa9glement\xc3\xa9.
• Exp\xc3\xa9rience dans le d\xc3\xa9veloppement et de la gestion du cycle de vie de produits.
• Exp\xc3\xa9rience dans la cr\xc3\xa9ation de calendriers de projets et de budgets.
• Excellentes aptitudes en mati\xc3\xa8re de r\xc3\xa9solution de probl\xc3\xa8mes dans un environnement d\'\xc3\xa9quipe.
• Excellentes aptitudes en mati\xc3\xa8re d\'organisation, de communication et de collaboration.
• Excellentes aptitudes en mati\xc3\xa8re de documentation.

Qualifications souhait\xc3\xa9es

• Certification en PGP
• Connaissance des normes ISO 13485 et FDA 21, CFR Part. 820.
• Connaissance de la norme ISO 14971.

About the roleAt Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we\'re solving some of the most important healthcare industry challenges. Together, we\'re one global team committed to making a difference in people\'s lives around the world. This is a place where you can find a career with meaningful purpose-improving lives through your life\'s work. We are looking for a R&D Systems Project Lead who can bring strong knowledge and application of technical and business concepts, procedures, and practices in project engineering. Someone who can interpret company policies and procedures to resolve issues related to biomedical application. We are looking for strong knowledge of product development life cycle management.Your responsibilities will include:

• Participates in the planning, execution and finalization of projects according to strict deadlines, within budget and by following organized and repeatable procedures.
• Participates in creating and maintaining project schedules.
• Coordinates the efforts of team members and third-party contractors or consultants in order to deliver projects according to plan.
• Acts as a liaison with project stakeholders and effectively communicates project expectations to team members and stakeholders in a timely and clear fashion.
• Identifies and manages project dependencies and critical path items while ensuring project quality and utilizing and following appropriate methodologies.
• Conducts project postmortems and communicates lessons learned in order to identify successful and unsuccessful project elements.
• In all actions, demonstrates a primary commitment to patient safety and product Quality by maintaining compliance to the Quality Policy and all other documented Quality processes and procedures.
• Other duties as required.

Required qualifications:

• B.Eng, MSc in Biomedical, or related field
• 4+ years of experience with product development activities in a regulated industry
• Experience in product development and life cycle management
• Experience with creating project schedules and creating budgets
• Strong problem-solving skills in a team environment
• Excellent organizational, communication and collaboration skills
• Strong documentation skills

Preferred qualifications:

• PMP Certification
• Knowledge of ISO 13485 and FDA 21 CFR Part 820
• Knowledge of ISO 14971

Requisition ID: 588854As 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!

Boston Scientific