R&d Project Manager

1 month ago

Montréal QC, Canada Boston Scientific Corporation Full time

**Work mode**:Hybrid**Onsite Location(s)**:Montreal, QC, CA**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.**À propos du poste**Responsabilités**
- Participer à la planification, à l’exécution et à la finalisation des projets, tout en respectant des délais stricts et le budget imparti et en suivant des procédures organisées et reproductibles.
- Participer à l’élaboration et à la mise à jour des calendriers des projets.
- Coordonner les efforts des membres de l’équipe et des sous-traitants ou d’experts-conseils externes afin de faire en sorte que les projets puissent être réalisés conformément au plan établi.
- Assurer la liaison avec les parties concernées par le projet et communiquer efficacement les attentes du projet aux membres de l’équipe et aux autres parties concernées en temps opportun et de manière claire.
- Recenser et gérer les contraintes et les éléments critiques de la réalisation des projets, tout en assurant la qualité des produits et en utilisant et en suivant les méthodologies appropriées.
- Effectuer des analyses rétrospectives des projets et en communiquer les conclusions afin de mettre en évidence les réussites et les lacunes observées.
- Faire preuve en tout temps d’un engagement inconditionnel envers la sécurité des patients et de la qualité des produits en respectant la politique d’assurance de la qualité et tous les autres processus et procédures documentés à cet égard.
- Effectuer d’autres tâches le cas échéant.

**Qualifications requises**
- Baccalauréat en génie, maîtrise dans le domaine biomédical ou dans un domaine connexe.
- Au moins quatre années d’expérience dans le domaine du développement de produits au sein d’un secteur réglementé.
- Expérience dans le développement et de la gestion du cycle de vie de produits.
- Expérience dans la création de calendriers de projets et de budgets.
- Excellentes aptitudes en matière de résolution de problèmes dans un environnement d’équipe.
- Excellentes aptitudes en matière d’organisation, de communication et de collaboration.
- Excellentes aptitudes en matière de documentation.

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

**About the role**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**:594991- **Job Segment**:R&D, R&D Engineer, Biomedical Engineering, Project Manager, QC, Research, Engineering, Technology, Quality

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