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Process Quality Engineer 2
hace 2 semanas
**Job Title**: Process Quality Engineer 2
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. An unwavering sense of purpose 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.
**Job Overview**
The Process Quality Engineer will work primarily with manufacturing processes and engineering counterparts in Advanced Engineering or Design Assurance in support of product inspections, and product and process compliance to established procedures and will take corrective and preventive action as required by procedures to support the continued operation of the Costa Rica site manufacturing lines as well as the introduction of new manufacturing line processes, or transfer of existing processes from other facilities into Costa Rica.
**Responsibilities**
- Assure that the products meet Philips requirements, regulations and standards.
- Ensuring that the requirements of the Intercompany Quality Agreement are met.
- Monitor daily work operations
- Support new product development and/or design changes in coordination with management, project leaders, & project team.
- Oversee, own, and review Nonconformance's, Product Holds and CAPAs for manufactured products.
- Position will assure that products and processes will be reviewed, tested, inspected, recorded, qualified, and released.
- Position will participate in audits with regulators, agencies, and auditors such as FDA, Competent Authorities and notified bodies. And support post market surveillance and recall activities, as needed.
**Requirements**:
- ** Intermediate/Advanced English**:
- Bachelors or master’s degree required, Engineering or Science preferred
- Typically requires a minimum of 1 + years of FDA regulatory industry required (Medical Devices, Pharmaceutical, or combination)
- CQE, CBA, or CQA are preferred
- Must have demonstrated ability to work with senior leaders and be able to engage/influence cross functional leadership teams
- Knowledge of methodologies for inspection test tools is preferred
- Knowledge of statistical methods and the use of standard quality tools (e.g. flowcharts, Pareto charts, cause and effect diagrams)
- ** Onsite**
**You are a part of**
A leading health technology company with a multinational workforce of approximately 77,000 employees and globally present with sales and services in more than 100 countries worldwide.
**In return, we offer you**
In order to develop your full potential, we will offer you the flexibility, encouragement and opportunities to keep you inspired and engaged. After all, working at Philips is more than a job. It is an experience full of amazing moments that will transform you in a lasting and positive way, since together we can improve the world.
**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.
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