Senior Quality Engineer - Hiring Immediately

We are hiring a resourceful Senior Quality Engineer to join our stellar team at Respironics Inc in China.
Growing your career as a Full Time Senior Quality Engineer is an amazing opportunity to develop competitive skills.
If you are strong in communication, creativity and have the right experience for the job, then apply for the position of Senior Quality Engineer at Respironics Inc today!


Job Title
Senior Quality EngineerJob Description Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation. Driven by the vision of a better tomorrow.
But it's not just what we do, it's who we are. We are 80,000, wonderfully unique individuals, with two things in common. and a relentless determination to deliver on our customers' needs. It's what inspires us to create meaningful solutions - the kind that make a real difference - when it matters most.
The world and our customers' needs are changing faster than ever before and while we are proud of what we do already, we know we can do more. That's why we need you, to help us tackle increasingly complex challenges posed by ever evolving health and well-being needs.
In this role, you have the opportunity to make life better Looking at the challenges the world is facing today Philips' purpose has never been more relevant. So whatever your role, if you share our passion for helping others, you'll be working towards creating a better and fairer future for all.
In this role, you have the opportunity to
Responsible for achieving a state of high quality performance, compliance and sustainability in the factories while pursuing continuous quality improvement through the application of Quality Engineering practices. Oversight of Philips products/parts/services utilized in manufacturing throughout the manufacturing lifecycle including sustaining change management.
You are responsible for
. To formulate and implement the Business' long-range quality, regulatory and compliance policy
. Create Q&R awareness level as determined within the organization.
. Enforces (a simplified) quality systems and harmonizes them across the Business sites and Sector establish an effective Management Review process, including routine reporting.
. Introduce and implement the quality processes and tools required to ensure product quality and customer satisfaction.
. Manages compliance to FDA regulations and other Regulatory Agencies as required, guidelines and policies to all products and operations are consistent with those regulations.
. Manages the review and approval of finished products manufactured for and by the company in accordance with their approved specifications. Includes Complaint handling
. Manages all inspections and questions relating to the operation of the manufacturing sites in coordination with all other applicable company groups
. Manages product recall activities to include recall policies and procedures for the company. Additionally, manage product compliant activities and processes.
. Direct the Audit Program for the organization.
. Drafts and manages the strategic improvement processes ('breakthrough Program') in the Business (One Page Strategy, Hoshin Plan).
. Interact with all areas involved in the product development process, customer services and sales and marketing and provide direction and consultation. You are a part of
. Directly reports to Manufacturing Quality Manager To succeed in this role, you should have the following skills and experience
. Bachelor Degree Or Above, major in Mechanical & Electronic Engineering or Equivalent
. Experience of medical device standard and regulatory requirement ISO13485, QSR, GMP.
. Fluent English both in writing and speaking
. Excellent communication and interpersonal skills
. Good training skills able to generate, following and explain detailed instructions and inspection procedures of the responsible areas accurately.
. Familiar with analytical tools, such as FMEA, process control plan
. Solid knowledge/experience in SPC, GRR & Process Capability Analysis
. Lean, problem solving and project management skill.
. High morale with excellent work ethic, integrity and attitude.
. Teamwork orientated, Self-motivated & able to Work Independently
How we work at Philips
Our newly-adopted hybrid work concept fuses flexibility with collaboration to deliver great outcomes for our people and our customers. We are embracing an approach wherein we spend more time together than apart - which for full-time employees translates to an average of at least 3 days working from the office and up to 2 days from home - for our hybrid roles.
Hybrid work flexibility means people can meet the changing demands of work and home in the most balanced, productive, and healthy way.
Our hybrid working model is defined in 3 ways:
There's a certain energy when everyone's in the same room that can heighten idea generation and creative friction needed for problem-solving.
Choosing where, when and how to work can vary according to task and team schedules. Flexibility isn't office or online, it means choosing the space that works best for you, your teams and our customers on a case-by-case basis.
The way we work and our workspaces are designed to support our well-being, offer career advancement opportunities, and enable us to be at our best.
Why should you join Philips
Working at Philips is more than a job. It's a calling to create a healthier society through meaningful work, focused on innovative, customer-first health technology solutions. Help us improve the health and well-being of billions of people, every year. Ultimately creating a career that no one could have planned for. Even you.

Benefits of working as a Senior Quality Engineer in China:

● Company offers great benefits
● Advancement opportunities
● Competitive salary