Philips Quality Engineer Products Systems 

South Africa, Free State, Dihlabeng Local Municipality 

406496270

Quality Engineer Products and Systems
Job Description

The Quality Engineer Products and Systems is accountable for quality oversight of system, hardware and risk management throughout the product life cycle.

Your role:

• Ensures that appropriate quality, reliability‐and Post Market Surveillance (PMS) plans are made and include all stages of the product life cycle

• Supports Quality Plan design for hardware and Software design and ensure they meet quality and compliance standards for every planned milestone. Validates key design inputs like usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs.

• Provides effective oversight of the execution of the quality, reliability, PMS Plans, any Risk Management activities, and all of design related activities during the product/system lifecycle.

• Performs independent technical assessment on product quality performance and post‐market product quality analysis to lead quality related problem solving and root cause analysis during design and manufacturing and initiates field actions when required.

• Supports stakeholders during the execution of quality system‐and product audits and inspections. Provide quality engineering support, including assisting organizational units in leading resolution of quality engineering deficiencies.

You're the right fit if:

• You have 1+ years of experience the medical device or other regulated industry, working on issues where analysis of situations or data requires review of relevant factors and exercising judgment within procedures and policies to determine appropriate action.

• You have experience producing and completing quality engineering documents, performing timely detailed quality engineering tasks including assessing product designs and reviewing test and other performance data, analyzing market feedback, completing or assisting with root cause analysis and quality problem solving.

• Your skills include a basic understanding of the Quality System Regulations (ISO 9001, ISO 13485, 21 CFR Part 803, 806 & 820) and knowledge of medical device process requirements.

• You have a bachelor’s degree in engineering with 5+ years of or equivalent experience.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

• You’re a developing professional who applies company policies and procedures to resolve a variety of issues. And you frequently interact with supervisors and/or functional peer groups in interactions normally requiring the ability to gain cooperation of others, conducting presentations of technical information concerning projects and schedules.

How we work together

This is an office role.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about .

• Discover

• Learn more about

• Learn more about our commitment to .

The pay range for this position in Massachusetts is $63,504 to $108,864 annually.

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

within commuting distance of Cambridge, MA. USA