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You will be updated with latest job alerts via emailPosition Overview:
The Supplier Quality Engineer supports complex and strategic projects which maintain and enhance the Convatecs Global Supplier Quality program
Your Key duties and Responsibilities:
Support the maintenance and improvement of ConvaTecs 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:
Bachelors 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 youll find them. Stretch your
thinking and youll 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 thatll move you.
#LI-AP1
#LI-Remote
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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!
Full-Time