Lead Specialist, Quality, Design Quality Engineer

Waukesha, WI - USA

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

Job Description Summary

In this role as QA Lead Engineer you be will responsible for providing manufacturing and/or engineering process support in accordance with documented procedures and practices. This is a key technical role responsible for the development implementation improvement and continuous reinforcement of established Quality Management System practices product specifications and applicable standards. You will collaborate within the areas of design design transfer manufacturing distribution and service.

GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition turn ideas into world-changing realities and join an organization where every voice makes a difference and every difference builds a healthier world.

Job Description

Roles and Responsibilities

Creates a Quality culture by driving compliance activities around a specific product site or region. This includes being responsible for the total quality management system for the business and driving Quality metrics.
Ensures quality and regulatory compliance while driving process effectiveness and efficiency.
Represents GE Healthcare to external agencies and champions the evolution of the quality culture which includes executing and driving quality objectives metrics reporting and operating mechanisms.
Develops in-depth knowledge of the product and processes. Uses prior experience and acquired expertise to execute functional policy/strategy.
You will be an individual contributor with demonstrated interpersonal skills. Communication with direct colleagues and the business about design and related processes (design transfer manufacturing distribution and service). Provides guidance to team members and explains complex information to others in straightforward way.
Impacts projects processes and procedures in own field. The role operates with some autonomy but is focused on execution of activities/processes. Activities require professional judgment but may require more senior levels of guidance.
Utilizes technical expertise and judgement to solve problems. Leverages technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions.
Supports continuous product and process improvement through detailed failure analysis for non-conformances investigations develops and implements effective and compliant solutions for product and process corrections retrospective and remediation action plans and for corrective and preventative actions (CAPA process)

Required Qualifications

Bachelors degree from an accredited university or college (OR a high school diploma / GED with at least 6 years of relevant work experience).
At least 3 years of relevant experience in Quality Assurance in a regulated industry e.g. Medical Devices.
Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas now or in the future for this job opening.
Ability to communicate effectively in English (both written and oral)

Desired Characteristics

Demonstrated understanding of Medical Device QMS requirements and regulatory requirements including but not limited to
FDA CFR 21 820 and ISO 13485.
Experience in Quality Assurance Quality Engineering Design Engineering or Manufacturing Engineering in a regulated
industry.
Demonstrated expertise to effectively communicate within different functions and different levels of the organization around
QMS concepts including Design Controls Production & Process Controls Corrective & Preventive Action (CAPA) Risk
Management and Product Quality.
Demonstrated collaboration negotiation and conflict resolution skills.
Experience performing internal audits and participating in external audits.
Demonstrated understanding of design change document change control and manufacturing/production process change
control processes and methodologies.
Ability to demonstrate analytical problem solving & root-cause analysis skills along with experience leading and implementing
change.
Ability to handle tasks with competing priorities effectively.
Strong technical aptitude (i.e. able to read & comprehend technical documentation & provide technical feedback)

We will not sponsor individuals for employment visas now or in the future for this job opening.

Additional Information

GE HealthCare offers a great work environment professional development challenging careers and competitive compensation. GE HealthCare is anEqual Opportunity Employer . Employment decisions are made without regard to race color religion national or ethnic origin sex sexual orientation gender identity or expression age disability protected veteran status or other characteristics protected by law.

GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19 some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.

Relocation Assistance Provided: No

Required Experience:

Job Description SummaryIn this role as QA Lead Engineer you be will responsible for providing manufacturing and/or engineering process support in accordance with documented procedures and practices. This is a key technical role responsible for the development implementation improvement and continuou...