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R&D Document Control Specialist / spécialiste du contrôle documentaire
full-timeMontreal

Summary

Location

Montreal

Type

full-time

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About this role

Bachelor's degree or equivalent in a related field. 2+ years related experience in the medical device industry. 2+ years' experience managing documentation and complex activities. Experience managing multiple electronic documentation systems and processing documents and drawings for approval. A knowledge and understanding how regularly available information is developed and maintained including drawings, design specifications, AML/AVLs and internal bills of material (BOMs). Experience managing electronic documentation systems and processing documents and drawings for approval. Excellent organizational, communication and collaboration skills. Excellent documentation skills. Experience using electronic document systems such as Windchill. Ability to work under limited supervision and manage multiple tasks and prioritize assignments with limited time constraints while working consistently in a fast-paced environment. Flexibility and ability to adjust to changing priorities and unforeseen events. Baccalauréat ou diplôme équivalent dans un domaine connexe. Minimum de 2 ans d'expérience pertinente dans l'industrie des dispositifs médicaux. Minimum de 2 ans d'expérience en gestion de la documentation et d'activités complexes. Expérience dans la gestion de multiples systèmes électroniques de documentation et le traitement de documents et de dessins pour approbation. Connaissance et compréhension du développement et de la maintenance de l'information couramment utilisée, incluant les dessins, les spécifications de conception, les AML/AVL et les nomenclatures internes (BOM). Excellentes compétences organisationnelles, de communication et de collaboration. Excellentes aptitudes en rédaction et en gestion de la documentation. Expérience avec des systèmes électroniques de gestion documentaire tels que Windchill. Capacité à travailler avec une supervision limitée, à gérer plusieurs tâches simultanément et à établir les priorités dans des délais serrés, tout en évoluant dans un environnement dynamique et rapide. Flexibilité et capacité d'adaptation face aux priorités changeantes et aux situations imprévues. Processus d'avis de modification (CN) : traiter les CN à travers les différentes étapes du processus, incluant la création du CN, la revue de la soumission, la mise en œuvre et l'émission des documents (gestion de la distribution des documents au besoin).

Other facts

Tech stack
Documentation Management,Medical Device Industry,Organizational Skills,Communication Skills,Collaboration Skills,Documentation Skills,Electronic Document Systems,Windchill,Task Management,Prioritization,Flexibility,Problem Solving,Design Specifications,Bills Of Material,AML/AVL Management,Change Notice Processing

About Boston Scientific

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 40 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of health care. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions.

For more information, visit www.bostonscientific.com and connect with us on X, Instagram, and Facebook.

At Boston Scientific, you will find purpose, a place to grow and opportunities to cultivate your passions. To search and apply for open positions, visit https://bostonscientific.eightfold.ai/careers.

You may also review our social media guidelines at http://www.bostonscientific.com/social.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Medical Equipment Manufacturing

What you'll do

  • The R&D Document Control Specialist will manage documentation and complex activities within the medical device industry. This includes processing documents and drawings for approval and overseeing the change notice process.

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Frequently Asked Questions

What does a R&D Document Control Specialist / spécialiste du contrôle documentaire do at Boston Scientific?

As a R&D Document Control Specialist / spécialiste du contrôle documentaire at Boston Scientific, you will: the R&D Document Control Specialist will manage documentation and complex activities within the medical device industry. This includes processing documents and drawings for approval and overseeing the change notice process..

Why join Boston Scientific as a R&D Document Control Specialist / spécialiste du contrôle documentaire?

Boston Scientific is a leading Medical Equipment Manufacturing company.

Is the R&D Document Control Specialist / spécialiste du contrôle documentaire position at Boston Scientific remote?

The R&D Document Control Specialist / spécialiste du contrôle documentaire position at Boston Scientific is based in Montreal, Canada. Contact the company through Clera for specific work arrangement details.

How do I apply for the R&D Document Control Specialist / spécialiste du contrôle documentaire position at Boston Scientific?

You can apply for the R&D Document Control Specialist / spécialiste du contrôle documentaire position at Boston Scientific directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Boston Scientific on their website.