R&D Packaging Engineer III

4 weeks ago

Mississauga, Ontario, Canada Boston Scientific Full time
About the Role

The R&D Packaging Engineer III will play a key role in developing new technology, products, equipment, and processes with minimal supervision. This individual will be responsible for compiling and analyzing operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials.

Responsibilities
  • Support complex cutting-edge medical device systems through prototyping, testing, and modeling.
  • Develop device design history files, including requirements, risk management, and usability files.
  • Ensure compliance to industry and international standards, including ISO 13485, ISO 14971, 21 CFR part 820, ISO 11135, and ISO 11607.
  • Develop verification and validation plans, protocols, and reports.
  • Perform independent tests, studies, analyses, and interpretations to generate technical conclusions and provide recommendations.
  • Conduct work across the full scope of technical and documentation activities for the department.
  • Make independent studies, analyses, interpretations, and conclusions.
  • Responsible for technical input into project-level planning.
  • Provide technical guidance to review work plans and advise on unusual features of projects.
  • Provide technical, project-level leadership to engineering assistants or junior engineering staff.
  • Support regulatory filings to various government bodies as required.
Requirements
  • Bachelor's degree in engineering.
  • 3+ years of related working experience in medical devices or a similarly regulated manufacturing industry.
  • 2+ years of relevant design control experience.
  • Experience with the overall design and development process.
Preferred Qualifications
  • Experience focusing on R&D activities relating to electro-mechanical equipment in the medical devices industry.
  • Experience designing packaging for medical devices.
  • Knowledge of ISO 13485, ISO 14971, 21 CFR part 820, ISO 11135, and ISO 11607.
  • Self-starter with the ability to quickly learn about new processes.
  • Excellent analytical and communication skills (both written and oral).
  • Able to work independently and in a multidisciplinary team environment.

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