-Under limited supervision, leads cross-functional teams to successfully complete assigned projects.
-Applies project management processes (including definition, planning, risk management, project control, and change management) to ensure that activities are carried out according to the timeline and budget.
-Reports on project performance metrics.
-Provides the needed design and technical expertise to properly identify and document all product, tooling and process specifications.
-Performs as an individual contributor and/or supervisor depending on the demands of a given project or group of projects.
-Collaborates with customers to ensure harmonious project coordination throughout the entire development process.
-Supports all departmental strategies and corporate goals and objectives.
-Frequently provides technical advice, expertise and support to other product development engineers and designers. May be considered an expert in a specific area.
-Identifies new materials and processes as required.
-Insures compliance with ISO, FDA and other applicable regulations.
-Understands, practices, and enforces corporate policies and procedures.
-Remains up-to-date on market requirements & trends and suggests creative ways to improve designs from both cost and functional perspectives.
-Initiates continuous improvements programs.
-Recommends methods for increasing customer value.
-Assists with budget creation and management.

EDUCATION / EXPERIENCE: Bachelor's degree in Mechanical Engineering required (preferably in bio-medical engineering with a mechanical focus). Five or more years experience in product development for the medical device industry required, preferably in Orthopedics. One or more years experience in a leadership or supervisory role required.

SKILLS:
-Strong leadership and interpersonal skills required.
-Ability to prioritize and complete multiple projects of varying degrees of complexities.
-Ability to develop team members both professionally and personally.
-Excellent written and verbal communication, organizational, planning and presentation skills required.
-Ability to negotiate with and influence others.
-Self-starter/motivator for personal and professional growth.
-Ability to form partnering relationships with peers and multiple levels throughout the organization.
-Knowledge of various metal and polymer materials.
-Knowledge of mechanical and anatomical testing requirements for Orthopedics.
-Knowledge of ISO13485 and US QSR 21 CFR, Part 820 Medical Devices.
-Knowledge of geometric dimensioning and tolerance practices (GD&T).
-3D CAD modeling experience preferred (Unigraphics, Pro-E, or Solidworks).