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Monday, May 24, 2010

Engineering Prog Mgr

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Date: May 24, 2010
Location: Montreal, QC, CA

Engineering Prog Mgr

Requisition 71628
Category Engineering
Business Cardiac Rhythm Disease Mgmt
Division AF/Cryocath
Location CAN-Quebec-Montreal
Relocation Relocation eligibility to be determined
Job Type Full Time - Regular
Exempt/Non-Exempt Exempt
Shift First
Travel Percentage 10 - 20%
Experience Required 5 years
Education Required Bachelor of Engineering

Medtronic is an Equal Opportunity/Affirmative Action Employer

Position Description

Sustaining Project Manager responsible for determining improvements in product performance, identifying solutions, and executing manufacturing and design changes.

Position Responsibilities

* Leads a team of engineers within a high growth, fast paced organization focused on the development of intracardiac medical devices to treat cardiac disease and improve patients' lives.
* Integrates information from a variety of internal and external sources to understand product performance across the portfolio.
* Identifies areas of improvement, develops action plans, reviews them with internal stakeholders, and leads the team through the execution phase.
* Manage projects and activities in a multiple project environment with high demand schedules.
* Work closely with the Quality organization to understand field performance of product portfolio. Identify areas of potential improvement and develop plans to address them.
* Lead a team of mechanical and electrical engineers in the development of solutions to complex problems
* Understand the needs and opinions of the clinician customer and how to incorporate them into design solutions
* Execute engineering solutions within the regulatory structure of the medical device environment.
* Ensure a systems thinking competency is maintained within the group
* Interface with external suppliers and manage those relationships as necessary to achieve project objectives.
* Develop and manage staff including establishing team objectives and annual performance reviews
* Generate documentation, supporting data and data analysis, reports, and presentation materials on to communicate within the organization and up to general management.
* Guide successful completion of projects through collaboration with Development, Manufacturing, Supply Chain, Quality, regulatory organizations and outside suppliers.
* Responsible for addressing assigned CAPA activities and ensuring that established timelines are met.

Basic Qualifications

* Bachelors Degree in Mechanical, Electrical, or Industrial/Manufacturing Engineering
* 5+ years engineering experience
* 3+ years Project Management experience
* Solid Mechanical Design experience within a design control process
* Experience with electromechanical systems
* Experience with Lean six sigma
* Must be familiar with manufacturing and design control processes in a regulated environment.

* Excellent communication skills with reports, peers, and management
* Ability to coach and mentor junior staff
* Experience with Corrective and Preventative Action systems including root cause analysis, identification of corrective actions, documentation to maintain compliance with the CAPA process, identification of appropriate effectiveness checks and collection of supporting data.
* High energy, self motivated individual in a diverse team

Desired/Preferred Qualifications

* Masters Degree with relevant business experience
* PMP certification

Physical Job Requirements

Job Segments: CAPA, Compliance, Data Analyst, Electrical, Electrical Engineering, Engineer, Engineering, Healthcare, Law, Lean Six Sigma, Legal, Management, Manager, Manufacturing Engineer, Medical Device, Medical Device Engineer, Medical Technology, Operations, Project Manager, Six Sigma, Supply, Supply Chain, Technology

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