Senior Quality Systems Engineer- Manufacturing

1 month ago

Auckland, New Zealand Fisher & Paykel Healthcare Full time

Senior Quality Systems Engineer- Manufacturing Quality Assurance & Control (Manufacturing, Transport & Logistics) Full time Our story began more than 50 years ago, when one doctor and two engineers designed a better way to care.
Today, we are a thriving global business, and our products, used in acute and chronic respiratory care, surgery and the treatment of obstructive sleep apnea, make a difference to millions of patients every year.
About Us Fisher & Paykel Healthcare is a world leader in the design, manufacture, and marketing of medical devices, exporting to over 120 countries globally.
We are an iconic New Zealand company with a consistent growth strategy ensuring an expanding range of innovative devices for use in respiratory care, acute care, and the treatment of obstructive sleep apnea.
Our commitment to excellence extends to our Quality Manufacturing team, an integral part of our operations.
The Quality Manufacturing team plays a crucial role in maintaining high manufacturing standards and improving the efficiency and effectiveness of the manufacturing processes and systems.
About the Role In this exciting role as a Senior Quality Engineer - Manufacturing, you'll actively collaborate with Operations, Production, and Process Development teams.
Your QMS and statistical expertise will be key in providing training and guidance to uphold quality standards for both new and existing processes.
Additionally, you will contribute to identifying and implementing improvements in our Quality Management System.
A practical attitude, coupled with a willingness to collaborate, is crucial for success in this role, alongside a proactive nature and results-focused approach.
Offering involvement across every function of the business and exposure to a variety of products and manufacturing processes, this is a permanent role at our Auckland site that will help you develop a strong understanding of the broader business.
Skills & Experiences 5+ years of work experience in Quality Engineering in the medical device industry.
A tertiary qualification in Science or Engineering.
Working knowledge of standards and regulations (ISO13485, ISO14971, 21 CFR Part 820, MDR).
Experience with process and test method validation activities.
Working knowledge of statistics and process improvement tools.
Six Sigma or CQE certification is preferable.
You will also have: Excellent communication skills both written and verbal with the ability to share complex ideas, positively influence, negotiate, and challenge with tact and diplomacy.
Strong problem-solving ability, both through your own independent thinking and collaboration across the business.
An ability to build relationships at all levels within the organization.
Requisition ID: 5027 Posting end date: 22/10/2024 #J-18808-Ljbffr

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