Supplier Quality Engineer

Description

Phillips-Medisize A/S is part of the Pharmaceutical and Medical Division of Molex, a leader in the design, development and delivery of advanced drug delivery devices and connected health solutions.

Phillips-Medisize A/S is collaborating with leading pharmaceutical companies worldwide by offering innovative and integrated solutions supported by an end-to-end service from Strategy to Production. At the site in Struer we do product and process development as well as assembly of devices. Read more about Phillips-Medisize A/S at phillipsmedisize.com.

If you have experience with quality assurance at suppliers worldwide, building strong relationships, and you have a very good sense of good documentation practice - then you could be the person, we would like to welcome to our team in Phillips-Medisize’s Global Innovation & Development Center based in Struer or Virum Copenhagen.

What You Will Do In Your Role

Our new Supplier Quality Engineer will participate in activities both during product development and in running production.

Part of the Supplier Control activities are covered by a divisional team, therefor the focus is the hands-on activities ensuring components are meeting specifications in corporation with the suppliers.

As part of Quality Assurance of Components you will:

• Assess each component to determine needed activities

• Agree on a component quality agreement with the supplier

• Ensure part approval of new and changed components
• Ensure process qualification of new and changed components
• Ensure corrective and preventive actions if components do not meet specifications or documentation requirements are not met
• Support the incoming control and suppliers in their activities
• Be very accurate and timely in your documentation practice
• Work together with the sourcing team and project teams ensuring right quality, price, and time – perhaps follow up on the timeliness in your teams

You will also actively contribute to develop and improve our procedures and best practice.

As part of supplier selection, approval and maintenance you will

• Participate in supplier selection, approval and classification
• Participate in supplier monitoring, improvement, follow-up and audits
• Participate in supplier development
• Work together with the divisional team carrying out the tasks

The Experience You Will Bring

Requirements:

• You have experience from a similar position
• You have a technical background within engineering and have knowledge about different production technologies
• You are structured and can work in accordance with a defined process
• You have very strong documentations skills
• You are proactive, result oriented and a self-motivated team player
• You are a good communicator and are fluent in English
• You have a global mindset and know how to navigate in different cultures

What Will Put You Ahead

• Experience from working with one or more production processes: Plastic injection molding, PCBA manufacturing or electromechanical assembly
• Experience from the medical industry and have knowledge about the requirements for the supplier processes from ISO 13485 / IATF 16949 (e.g. PPAP, SPC, MSA, FMEA, Dimensional results, validation)
• Experience with SAP

#LI-IB1