Sr Engineer, Quality

Masimo Corporation; Mitchells Plain; On-site; USD 80 000 - 130 000; Full time

Job summary

An innovative firm is seeking a Quality Engineer to join their Product Assurance team. This multifaceted role involves ensuring quality throughout the product lifecycle, from design to post-market. The ideal candidate will possess strong engineering knowledge and a commitment to quality improvement. You will engage in problem-solving activities, maintain compliance with international standards, and collaborate with cross-functional teams to enhance product reliability. If you're passionate about quality engineering and eager to make a significant impact, this opportunity is perfect for you.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401(k)

Paid Vacation

Flexible Spending Accounts

Employee Assistance Program

On-site Wellness Clinic

Qualifications

• 3 years of Quality Engineering/Quality Assurance experience required.
• Direct experience with ISO 13485 and FDA QSRs essential.
• Hands-on experience with statistical methods and problem-solving.

Responsibilities

• Support Product Assurance goals and maintain knowledge of regulations.
• Participate in problem solving related to design and manufacturing.
• Contribute to product and process risk analysis and management.

Skills

Quality Engineering

Quality Assurance

ISO 13485

FDA QSRs

Statistical Methods

Communication Skills

Problem Solving

Teamwork

Education

B.S. in Electrical Engineering

M.S. in a related Engineering discipline

Tools

Microsoft Office

PLM Systems

MMS Systems

ERP Systems

Job description

Job Summary

The Quality Engineer position at Masimo is a multifaceted role that requires a wide breadth of engineering knowledge. An individual in this role will work as part of the Product Assurance department to help drive quality in the company's growing product portfolio. As an integral part of the product development team, quality engineers help guide and direct the team to produce quality products. As a result, a person in this position should be comfortable in all facets of quality engineering through all stages of a typical product lifecycle (Design, Verification and Validation Testing, Production, and Post-Market). A successful person in this role will exhibit the following: Excellence in working in a team environment, Strong engineering knowledge, Good understanding of quality engineering, Commitment to a career in quality, Ability to take on and overcome challenges, and have a general interest in improving products and processes.

Duties & Responsibilities

• Support the Product Assurance goal of driving making quality a competitive advantage;


• Maintain up to date knowledge of Quality System Regulations (FDA CFR 21 820), ISO 13485, Canadian Medical Device Requirements (CMDR), MDD 93/42 EEC and other applicable international medical device standards and regulations;


• Participate in problem solving activities related to design, manufacture, inspection, and test, including CAPA, NCR and supplier related issues;


• Solve identified issues through analysis, critical thought, and development of a clear set of recommendations to the team and management for resolution;


• Participates in in the improvement of product and manufacturing quality and reliability through tools appropriate for the project, such as test sample size selection, test method validations, Gage R&R studies, and SPC.


• Contribute as part of multi-departmental teams in product and process risk analysis and risk management activities, including the development of product and process FEMA and Risk Analysis reports.


• Ensures robust application of the quality system by supporting the entire Quality Management System including the CAPA, NCR, customer feedback activities, and product failure analysis;


• Develop and maintain Design History Files (DHF) for products;


• Perform other duties or special projects as requested.

Minimum & Preferred Qualifications and Experience

Minimum Qualifications

• 3 years of Quality Engineering/Quality Assurance experience;


• 2 years' experience in a medical device design, development, and manufacturing environment;


• Direct experience with ISO 13485 and FDA QSRs;


• Direct experience in Test protocol development and execution in support of new product development and/or failure analysis;


• Hands on experience implementing and using statistical methods throughout various aspects of product realization, including use of PFMEA, DFMEA, DOE and GR&R methodologies;


• Strong communication, documentation, problem solving and teamwork skills;


• Ability to occasionally travel domestically and internationally;


• Proficiency with Microsoft Office applications;


• Prior experience with PLM, MMS, ERP systems;

Preferred Qualifications

• Certified Quality Engineer (CQE)


• Experience with sterilization validations
  

Education

• B.S. in Electrical Engineering, Biomedical/Biomechanical Engineering, or a related science/engineering discipline is required.


• M.S. in a related Engineering or science discipline is a plus.

Compensation

The anticipated salary range for this position is $80,000 - $130,000 plus benefits. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. This position also qualifies for up to 10% annual bonus based on Company, department, and individual performance.

Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, Voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center and Cafe. All benefits are subject to eligibility requirements.

Physical requirements/Work Environment

This position primarily works in an office environment. It requires frequent sitting, standing and walking. Daily use of a computer and other computing and digital devices is required. May stand for extended periods when facilitating meetings or walking in the facilities. Some local travel is necessary, so the ability to operate a motor vehicle and maintain a valid Driver's license is required.

The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.

Masimo is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

***NO AGENCIES PLEASE*** Thank you!