Sr. Supplier Quality Engineer

hace 3 semanas

Alajuela, Costa Rica Philips A tiempo completo

**Job Title**:
Sr.
Supplier Quality Engineer

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.
**You are responsible for**

The Sr.
Supplier Quality Engineer will be responsible for providing Supplier Quality engineering support to Global supply base.
Position will directly support New Product Introduction (NPI) and modified product design projects.
Will have oversight of assigned NPI product launches and transfers, active review and management of non-conformances, creation and review of quality metrics, and developing and maintaining effective working relationships with suppliers consistent with quality and business goals.
- Provide R&D and Manufacturing Engineering (ME) project support across multiple commodities (e.g.
plastics, electronics, metals and chemicals) as the resident supplier development expert.
Work with suppliers to perform process and component material development work to ensure components/materials and sub-assemblies are qualified to the appropriate requirements prior to commercialization and/or design or revision changes.
Work with R&D, ME and the Supplier to clarify design intent and requirements and ensure supplier feedback is included in the supplier development process
- Develop current and future Supply base.
This includes partnering with suppliers (contract manufacturers, service providers, component manufacturers) on the development, manufacture and improvement of product(s), supplier assessments, and risk analysis, provide revision and maintenance of an Approved Supplier List, create, finalize, and maintain supplier Quality Plans/Agreements, issue and investigate supplier delivery, quality, and compliance related non-conformances using a systematic approach to problem solving, conducting risk analyses and drive corrective and preventative actions to successful closure
- Lead or participate in the audit and assessment of Suppliers ensuring they are compliant with associated policies/procedures and GMP/ISO/PMDA requirements.
May also include due diligence audits/assessments
- Develop and maintain a Supplier Performance Scorecards, analyze and identify emerging supplier non-conformance trends using appropriate statistical tools.
Report supplier quality trend data during Quality/Operations Site Review and Management Reviews

**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.
**To succeed in this role, you'll need a customer-first attitude and the following**
- Bachelor's degree in an engineering or a combination of equivalent job experience in related field.
- Advance English level.
- Statistical knowledge.
- ISO 13485 Lead auditor Certification is desirable.
- CQE and CQA certification is desirable.
- From 3-5 years in medical industry in areas related to Quality Assurance, Incoming Quality, or Documentation, Complaints.
- Knowledge in problem solving with quality tools such as: 6 sigma, 8-D, CAPA, 5WHYs.
- Experience in reviewing detailed records with a critical eye to documentation completeness and correctness based on established procedures.
**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.
**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.
For our hybrid roles, this translates to an average of three days working from the office and two days from

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