Senior Quality Engineer, New Product Introduction

Work Flexibility: Onsite

Senior Quality Engineer New Product Introduction

Irvine CA

Join Strykers Quality Engineering team supporting the introduction and transfer of new medical devices and manufacturing this role you will provide quality engineering support across risk management validation inspection supplier quality and design transfer activities while partnering with Engineering Manufacturing Design Assurance and Quality teams.

What you will do

• Support new product and process introductions by executing and documenting quality engineering activities throughout design transfer and product launch.
• Apply risk management principles to process risk assessments risk mitigation process controls and Process Failure Mode and Effects Analysis (PFMEA) in accordance with ISO 14971.
• Develop inspection strategies sampling plans First Article Inspection approaches and Measurement System Analysis (MSA) strategies to support repeatable and scalable manufacturing processes.
• Support the development execution review and approval of process validation protocols and reports including sterilization validation activities when applicable.
• Apply statistical methods and quality engineering tools to evaluate process capability identify risks investigate nonconformances and support corrective and preventive actions.
• Support Design for Manufacturing and Assembly through process design inspection optimization tooling and fixture development and production specification development.
• Execute supplier quality activities including supplier qualification validation Production Part Approval Process (PPAP) supplier certification and Quality Agreements.
• Partner with cross-functional teams during design reviews and design transfer activities documenting quality deliverables and transferring product and process knowledge to manufacturing and Quality Engineering teams.

What you will need

Required

• Bachelors degree in Engineering or a related technical discipline.

• Minimum 2 years of experience in quality engineering or technical discipline
• Experience in a regulated manufacturing environment.
• Experience with risk management and process controls.

Preferred

• Experience in new product or new process introduction.
• Certified Quality Engineer (CQE) certification or equivalent quality engineering coursework or experience.
• Experience with medical device manufacturing and quality requirements including ISO 13485 Good Manufacturing Practices and Good Documentation Practices.
• Lean Six Sigma training and experience with quality and statistical tools such as PFMEA MSA process capability statistical sampling and DMAIC.

• Experience with supplier qualification and supplier quality activities supporting new product introduction and manufacturing.

$89400 - $148900 USD Annual

Travel Percentage: 20%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.