Manager, Continuous Improvement And Manufacturing Engineering

Illinois Tool Works Norwood , MA 02062

Posted 2 months ago

Job Description:

Manager, Continuous Improvement and Manufacturing Engineering - Norwood, MA

Instron is a global organization that designs, manufactures, sells and services materials testing systems. Instron is a clear global leader in materials testing applications and its leadership in the marketplace is continually expanding. You will find that our established strength, commitment to our core values and team focus provides an engaging work environment and offers exceptional opportunities for personal and career development.

The Opportunity

Engineering Management role that straddles the line between R+D and Operations. Focus is on both continuous improvement of our existing static product line as well as driving operational excellence into the organization through the manufacturing engineering team. Leads a multi-discipline group of 10-12 engineers supporting new product launches, continuous improvements of existing products as well as support of the existing products in manufacturing. This role will report to the Director of Operations and interact directly with management in all departments across the organization.

Requirements

Successful candidates should possess a Bachelor's Degree in Engineering or Applied Science with at least 5 years in an engineering leadership role with a capital equipment manufacturer. Additional requirements include:

  • Support all released products and manage product design changes for the entire product life cycle (from launch through obsolescence).Assign resources to engineering projects, and develop a system to evaluate the priority of projects

  • Ensure that new designs meet acceptable Design for Manufacturability (DFM) through close engagement with new product development teams.Manage pilot builds and provide feedback to the design teams that seek to improve the quality and reliability of new products

  • Establish and maintain the factory production layout using sound Lean manufacturing techniques.Develop, maintain and improve production documentation, manufacturing equipment, and product testing methodology

  • Support the customer escalation process to ensure that customer problems are resolved in an effective and timely manner

  • Structured Problem-Solving Expert.(8D, Critical Thinking, Fault Tree, 5 Why) Drive effective root cause and corrective action (RCCA) for any non-conforming material or products.Trains and mentors the organization in the effective use of RCCA tools

  • Process Driven with the ability to create and modify critical business processes to meet the ever-changing business needs

  • Implement the ITW toolbox in manufacturing and lead continuous improvements with a focus on quality, cost reduction, and efficiency

Take this opportunity to join a successful and enthusiastic team where you can make a significant impact immediately. Enjoy a competitive salary and generous benefits that includes health, dental, life and LTD insurance, 401k (with a great match), and a 100% tuition reimbursement program.

Take this opportunity to join a successful and enthusiastic global team where you can make a significant impact immediately. Enjoy a competitive salary and generous benefits that includes health, dental, life and LTD insurance, 401k (with match), and a 100% tuition reimbursement program. Instron is an Equal Opportunity/Affirmative Action employer. We employ, train, compensate and promote regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Regulatory Project Manager Point Of Care

Siemens Corporation

Posted 1 week ago

VIEW JOBS 4/12/2019 12:00:00 AM 2019-07-11T00:00 Division: Siemens Healthineers Business Unit: Siemens Healthineers Requisition Number: 241214 Primary Location: United States-Massachusetts-Norwood Assignment Category: Full-time regular Experience Level: Senior level Education Required Level: Bachelor's Degree Travel Required: 15% Division Description: At Siemens Healthineers, we are passionate about enabling healthcare professionals to deliver high quality patient care, and to do so affordably. A leading global healthcare company, Siemens Healthineers continues to strengthen our portfolio of medical imaging and laboratory diagnostics, while adding new offerings such as managed services, consulting, and healthcare IT services – as well as further technologies in the growing market for therapeutic and molecular diagnostics. Siemens Healthineers develops innovations that support better patient outcomes with greater efficiencies, giving providers the confidence they need to meet the clinical, operational and financial challenges of a changing healthcare landscape. For more information, please visit: http://www.usa.siemens.com/healthineers Job Description: Regulatory Program Manager, POC The Regulatory Program Manager for Point-of-Care (POC) is fully responsible for project execution to establish compliance to the European In-vitro Diagnostics Regulation (IVDR) at POC. This covers all phases of the project through the mandatory compliance deadline. The position is responsible to achieve measurable implementation for all products planned to be placed on the European market after the compliance deadline. During project execution, this position keeps the cross-functional team focused on achieving the expected project results in a timely manner. The individual facilitates communications between team members, manufacturing sites and senior management to ensure business goals are met. As a Program Leader, responsibilities include: * Lead a cross functional team through a disciplined process of iterative planning and risk mitigation, action-oriented and timely execution, and team-based problem solving * Own, track and execute to the integrated project plan that guides critical activities and resources * Drive fast project decision making and trade-off assessments * Apply basic and advanced methods for problem solving and process optimization * Interface with functional managers for resource management * Interface with the larger "Euro 20/22" Healthineers program to assure consistency and information flow with Erlangen QT * Manage project communications to all stakeholders including escalating hurdles and bottlenecks to senior management * Drive implementation of required process changes at all impacted sites * Ensure compliance of the project execution, e.g. process adherence and completeness * Foster continuous improvement mindset within project team(s) and department Skills and Attributes: * Ability to coordinate across all disciplines of the business as they are needed for demonstrating IVDR compliance * Self-motivated initiative and discipline. The role requires self-direction and self-advocacy, knowing when to ask for help and when to provide guidance to team members * Experience in lean methods like Six Sigma, Agile or Business Systems for operational excellence * Strong analytical skills and data driven mindset * Experienced in anticipating risk and working on counter-measures * Excellent communicator, mediation skills, capable of working under changing conditions * Understanding of IVDR requirements and interfacing with Notified Bodies * Detailed knowledge of Quality Systems, including ISO 13485 Required Experience, Knowledge and Expertise: * Bachelor's degree in an analytical or operational major; Masters is preferred * 10-15+ years of general business experience, with at least 7 years working in an FDA-regulated environment * 5-10 years of progressively responsible experience working and leading in a project management environment * Direct experience planning and executing complex projects, with remote resources and technical complexity * Experience in regulatory submissions to Notified Bodies and Health Authorities (e.g. FDA) * Ability to travel within US and outside of the country Siemens Corporation Norwood MA

Manager, Continuous Improvement And Manufacturing Engineering

Illinois Tool Works