Project Engineer II

Position Summary

Under general direction, the Project Engineer, based in Morrisville NC, is responsible for leading sustaining engineering projects affecting medical devices of the Surgical Business Unit.  This position focuses on organizing and managing multiple projects and ensuring they are completed in a timely manner.  Assignments will primarily be focused on existing products within the portfolio, providing creative solutions to technical issues or modifying/improving the product as required.

The candidate must be capable of advanced level scope of assignments in planning, designing, and coordinating the development and implementation of related engineering activities to support changes and improvements to existing products lines, and implement successfully into manufacturing. Incumbent at this level self-manages their project work, seeks help when required, and is fully aware of the operating procedures and policies of the Surgical team.

Principal Responsibilities

•    Acts as product technology group owner/subject matter expert for assigned product lines.
•    Coordinates the product design and development process with appropriate support departments such as engineering, quality, regulatory, marketing, documentation, operations, procurement.
•    Serve as an R&D technical lead representative in transfer, integration, or other corporate initiative core teams. Collaborate with Engineering, Quality, and Regulatory to understand technical targets and design control systems. 
•    Serves as project leader for assigned projects; responsible to follow up on all aspects of projects. Reports project statuses and key metrics and dashboard updates to required systems.
•    Resolves complex process/product development and manufacturing issues; independently takes lead of working cross functional teams.
•    Prepares formal documentation of the product designs, change management, risk analysis, product requirements and specifications, customer needs, etc. according to established product development procedures.  Initiates formal reviews to progress projects to compliant completion. 
•    Prepares or coordinates development of design drawings, specifications, estimates of costs, documentation updates, etc. 
•    Utilizes appropriate PLM, ERP and other product-related database systems.
•    Conducts research on projects associated with the design and/or design modifications of medical devices, components, models, or mechanisms.
•    Develops, maintains, and publishes plans for assigned projects with critical milestones and timelines. Owns the change management activities for sustaining or supplier-initiated changes. Leads design transfer activities when required.
•    Develops and coordinates the execution of protocols for validations of new or modified devices or components, including validations of the design, test methods, manufacturing processes, assembly, packaging, and sterilization where applicable.
•    Primary R&D interface with operations for cost improvement projects, vendor materials, and finished goods qualifications.
•    Investigates and resolves technical production problems involving product performance.
•    International efforts (travel, interface) are key, as role supports new product development and sustaining engineering efforts for the manufacturing plants as applicable.  Teleflex is a global organization with manufacturing facilities in the US, Mexico, Czech Republic, Malaysia, India and Germany.
•    Consults with sales staff or customer on product requirements where design or manufacturing issues or changes are involved.
•    
•    Demonstrates professional responsibilities by cooperating with other personnel to achieve department objectives and maintain good employee relations, interdepartmental objectives, and departmental goals and objectives.
•    Drives quality improvements with PM tools including the following: risk assessment/ mitigation, project schedules, and budget forecasting.
•    Pursues continued development of engineering technical skills through project tasks such as design reviews, specification updates, engineering drawing review/updates, etc.
•    Demonstrates the ability to contribute to the larger R&D workstream through taking on diverse project management tasks 

Education / Experience Requirements

•    Bachelor’s Degree in Engineering or Equivalent 
•    Minimum 3-5 years of work experience in the development of devices within the medical device industry. 
•    Prior work in testing, validation and/or sustaining engineering is preferred, with close partnerships with manufacturing teams.  
•    Experience with SolidWorks CAD (design/drafting) program preferred
•    Microsoft Office Suite (Project, Word, Excel) required
•    Knowledge of Injection molding, metal processing and plastic part assembly, a plus
•    Experience working within the medical device-related industry requirements (FDA, MDD, MDR, ISO Standards, etc) 
•    Experience with Design Controls, a plus
•    Relational database experience (such as Oracle Agile) and ERP experience (SAP, Oracle) a plus
•    Testing experience using ISO and ASTM testing methods for medical devices and general plastic components preferred

Specialized Skills / Other Requirements

Skill Sets:
•    Strong written and verbal communication skills and attention to detail. 
•    Effectively present information and respond to questions from groups of customers, peers, managers, senior leadership.
•    Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists; interprets a variety of instructions furnished in written, oral, diagram, or schedule form.
•    Analyze complex, technical, and administrative problems and adopt an effective course of action.
•    Make effective presentations to, and participate in a variety of meetings and conferences with other companies 
Ability To:
•    Demonstrate creativity and ingenuity in applying engineering principles and practices.
•    Draw solutions form a wider range of experience.
•    Organize, evaluate, and coordinate engineering studies with professional, technical, and clerical staff of a product evaluation department.
•    Conduct comprehensive studies and preparation of reports including recommendations.
•    Prepare clear and concise statements and reports.
•    Establish and maintain cooperative relations with those contracted in the workplace.
•    Speak and write English fluently.

TRAVEL REQUIRED: 10% (Domestic US & International)

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