Project Engineer

Tibidabo Scientific Industries; Madison (CT); On-site; USD 90,000 - 120,000; Full time

Job summary

Tibidabo Scientific Industries in Madison, CT seeks an R&D Project Engineer to lead cross-functional teams, define scopes, and drive product development with strong emphasis on quality and schedule adherence.

The role requires 2+ years in project engineering and a biomedical background; MBA/tech-management is a plus. Travel up to 5% is expected as projects operate across multiple disciplines and suppliers.

Qualifications

• 2+ years in project engineering and product development.
• Experience leading ISO 9000 / 13485 environments.
• Experience managing multiple technical disciplines and budgets.
• Biomedical degree required; MBA/tech management preferred.
• Strong communication with stakeholders at all levels.

Responsibilities

• Lead R&D and cross-functional project engineering to meet quality and schedule commitments.
• Develop project scopes, objectives, and deliverables with stakeholders.
• Collaborate to accelerate system development (DFM, DFS).
• Track progress and provide updates to management.
• Engage with customers, advisors, suppliers, and partners.
• Manage operating expenses and CAPEX for projects.
• Serve as SME on engineering change and design control procedures.

Skills

Project management

Cross-functional leadership

ISO quality systems

Budget management

Engineering change control

Verbal communication

Travel up to 5%

Education

Biomedical engineering degree

MBA or MS in technology management

Tools

Office (Word, Excel, PowerPoint)

Job description

Summary Of Position

The R&D Project Engineer will be responsible for leading cross-functional teams to develop

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.
• Medical device experience preferred
• Six Sigma/Lean certified preferred

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