Project Engineer

Tibidabo Scientific Industries Ltd.

Madison (CT)

On-site

USD 85,000 - 120,000

Full time

4 days ago
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Job summary

Tibidabo Scientific Industries Ltd. in Madison, CT, seeks an R&D Project Engineer to lead cross-functional teams and define project scopes, objectives, and deliverables for product development.

You will execute plans to ensure on-time delivery, exceed quality standards, and engage with customers and suppliers while managing multiple technical disciplines across electro-mechanical systems.

Qualifications

  • Bachelor’s degree in Biomedical Engineering or equivalent with 2+ years in engineering.
  • Experience leading product development projects in regulated environments (ISO 9000/13485).
  • Proven ability to manage budgets, schedules and cross-functional teams.

Responsibilities

  • Lead R&D and cross-functional project engineering to define scopes and deliverables.
  • Develop and execute project plans to meet quality and schedule commitments.
  • Collaborate with stakeholders to accelerate system solution development (DFM/DFS).
  • Track progress and provide regular management updates.
  • Engage with customers, advisors, suppliers, and partners as a SME on design controls.
  • Manage project OPEX and CAPEX; ensure on-site delivery of programs.

Skills

Project engineering
Cross-functional leadership
Communications
Budget management
DFM/DFS awareness
Multidisciplinary coordination

Education

Biomedical engineering degree
Masters in technology management or MBA (desirable)

Tools

Office suite (Word/Excel/PowerPoint)

Job description

SUMMARY OF POSITION
The R&D Project Engineer will be responsible for leading cross-functional teams to develop
project scopes, objectives, and deliverables using best practices. They will execute project
plans to ensure on-time delivery and exceed quality standards in support of product
development

DUTIES AND RESPONSIBILITIES
  • Leading R&D and cross-functional project engineering and project management, developing
    and executing project plans to meet or exceed quality and schedule commitments
  • Develop project scopes, objectives, and deliverables using best-practice deployment in
    collaboration with cross functional project team stakeholders.
  • Cross-function collaboration to accelerate development of system solutions (e.g., DFM, DFS)
  • Track project progress and provide regular updates to management.
  • Effective engagement with customers, advisors, suppliers, partners, and other external
    stakeholders
  • Management of project operating expenses and CAPEX
  • Serve as a subject matter expert on engineering change and design control procedures
  • Performs all other duties as required to meet the company’s goals and objectives.
QUALIFICATIONS AND EDUCATIONAL REQUIREMENTS
  • Demonstrated experience ( >2 years) project engineering, talent development planning, and engagement with >3 technical associates
  • Demonstrated experience (>2 years) leading product development projects in an ISO 9000 or equivalent quality system environments (e.g., ISO 13485)
  • Demonstrated experience (>2 years) managing multiple technical disciplines (e.g., mechanical, electrical, and/or software) and systems
  • Financial acumen to manage project, Engineering/R&D budgets, statistics, and CAPEX (>2 years)
  • Effective communication skills with superiors, peers, and subordinates
  • Travel up to 5% on an annual basis including customer, partner, and supplier visits, and industry conferences
  • Biomedical Technical degree (Bachelors) with a minimum of 2 years professional engineering and product development experience
  • Strongly desired: Masters level technology management degree or MBA with technical concentration
  • Ability to support multiple projects/products simultaneously.
  • Full product cycle experience with electro-mechanical aspects of a system: design, develop, test, release, production.
  • Good documentation and organizational skills.
  • Use of Office (Word, Excel, and PowerPoint) and/or similar productivity tools in Windows PC environment to generate documents.

This position is located on-site, in Madison, CT.

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