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R&D Engineer III

Job in Mississauga, Ontario, Canada
Listing for: Boston Scientific
Contract position
Listed on 2025-12-28
Job specializations:
  • Engineering
    Product Engineer, Packaging Engineer, Biomedical Engineer, Manufacturing Engineer
Job Description & How to Apply Below

Additional Locations: Canada-ON-Mississauga

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.

Please note this is a 12-month contract opportunity.

About the role

We are seeking an R&D Engineer III to join our dynamic R&D Packaging and Sellable Product team. The engineer will work under limited supervision/ guidance to support the design, development and implementation of packaging solutions for our products in addition to working closely with cross-function teams, i.e. Marketing, Regulatory and Supply Chain, etc., to ensure successful product commercialization.

Your responsibilities will include:

  • Fully participating in project teams to contribute the necessary technical work related to packaging and product design and development
  • Technical analysis of medical device packaging systems and materials for new product development and existing products to ensure designs meet quality and regulatory standards
  • Gather requirements from internal and external sources to accurately capture user needs and ensure products are meeting them
  • Investigate field related issues and perform root cause analysis
  • Generate engineering documentation (e.g., DHF and DMR) in adherence to quality policies and systems.
  • May lead packaging specific initiatives to support new designs, materials, or process related issues.
  • Adhere to all requirements of the Quality Management System
  • Other duties as required
  • Required qualifications:

  • Bachelor’s degree in a relevant engineering discipline
  • 4+ years of related work experience
  • Experience working within a quality management system and quality system controls (e.g. design inputs/outputs, Verification/validation, etc.)
  • Strong analytical and problem-solving abilities
  • Strong oral and written communication skills, to communicate with individuals at various levels
  • Preferred qualifications:

  • Bachelor’s degree in mechanical or biomedical engineering strongly preferred
  • Experience working within medical device R&D departments, with hands-on prototyping and testing
  • Experience using CAD software (e.g., Solid Works)
  • Knowledge of packaging materials including paperboard, corrugate, flexible packaging films, Tyvek, thermoformed trays, and manufacturing methods.
  • Familiarity with industry related standards (e.g. ISO, ASTM, etc.) and their direct application
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