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Supplier Quality Engineer

Supplier Quality Engineer

ConvaTecWarsaw, Poland
10 days ago
Job description

Pioneering trusted medical solutions to improve the lives we touch : Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE : CTEC). To learn more about Convatec, please visit

We are guided by our five core values, that shape the way we work, every day : Improve Care, Deliver Results, Grow Together, Own It and Do What’s Right.

Change is everywhere at ConvaTec. It’s transforming our business and helping us improve millions of lives. And we’re nowhere near finished. Across every part of our business, we’re pushing for better.

Join us on our journey to #ForeverCaring as a Supplier Quality Engineer and you’ll do the same.

Position Overview :

The Supplier Quality Engineer supports complex and strategic projects which maintain and enhance the Convatec’s Global Supplier Quality program

Your Key duties and Responsibilities :

Support the maintenance and improvement of ConvaTec’s Global Supplier Quality program

Focus on establishing, maintaining and improving supplier performance metrics, policies, and procedures in administering quality relationships with suppliers globally.

Investigations relating to suppliers’ issues through the SCAR and CAPA process.

Internal Investigations through the NC and CAPA process.

Support and lead where appropriate, supplier selection, evaluation, and approval.

Conduct Supplier audits

Generate and monitor appropriate key performance indicators to assess supplier performance in a timely manner to drive resolution of corrective actions from the suppliers.

Raise appropriate questions or concerns regarding regulatory compliance to appropriate authorities regarding Purchasing Control activities.

Driving change requests through to closure for our ECCF and CCR process.

Demonstrate high commitment to quality and customer service based upon customer needs.

Build strong relationships with customers, suppliers, stakeholders, and support groups worldwide to meet the demands of a changing business environment.

Demonstrate technical knowledge and principles in relation to medical devices in line with ISO13485 ISO9001 GMP Parts 201 and 211, EU MDR.

The employee may be required to perform other duties as assigned by management or supervisors that are reasonably related to the job or necessary for the smooth operation of the organisation

Our requirements :

Bachelor's in science in Science or Engineering.

Minimum 2 years of experience in Supplier Quality Control within Medical Devices industries, working on audits, quality agreements, monitoring of suppliers, procedures updates and participating in Supplier Onboarding.

Experience in internal and supplier related CAPA / NC / SCAR initiation.

Experience working with QMS Softwares (Trackwise, Windchill, etc).

Knowledge of quality control principles and their relationship to relevant regulatory requirements.

Quality Auditor or Lead Auditor certification : ISO 13485.

Advanced computer management skills including Microsoft Word, Excel and Visio.

Our progress will give you countless opportunities to move forward

too. Seek out new challenges, and you’ll find them. Stretch your

thinking, and you’ll find new ways to make an impact. And if you

embrace the opportunity to drive your own growth, you could go

further, and achieve more, than ever before.

This is a big step forward.

This is work that’ll move you.

LI-AP1

LI-Remote

Beware of scams online or from individuals claiming to represent Convatec

A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.

If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at .

Equal opportunities

Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.

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Quality Engineer • Warsaw, Poland

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