Supplier Quality Engineer

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. Group revenues in 2022 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com

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.

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

Key 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 the 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
  
  
  

Authority (if applicable):

• Execution and sign off final release for third party product batches to support base business and to ensure compliance to specifications and documentation requirements.
  
  
  

Skills & Experience:

• BS or higher degree qualified in Science or Engineering
• Quality Auditor or Lead Auditor certification is preferred in ISO9001 or ISO13485
• Minimum 3 years of experience in the medical device industry
• Minimum 2 years of experience in Supplier Quality Control
• Experience in internal and supplier-related CAPA/ NC/ SCAR initiation.
• Knowledge of ISO13845 and FDA medical requirements.
• Statistical skills.
• Strong prioritization and coordination skills.
• Ability to work with electronic databases (i.e. Documentum, Trackwise, SAP).
• Advanced computer management skills including Microsoft Word, Excel, and Visio.
• Proactivity and flexibility to meet priorities and achieve deliverables
• Ability to negotiate and partner with internal and external customers to enhance operational effectiveness.
  
  
  

Travel Requirements

The position may involve travel up to 10% of the time to Convatec sites and supplier locations globally.

Working Conditions

Remote, presence at the local office may be required based on in-country legal requirements and for specific meetings/ projects/ events.

Our transformation will change your career. For good. You'll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you'll be supported to bring them to life. There'll be challenges. But stretch yourself and embrace the opportunities, and you could make your biggest impact yet.

This is stepping outside of your comfort zone.

This is work that'll move you.

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 [email protected].

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.

Notice to Agency and Search Firm Representatives

Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Already a Convatec employee?

If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!