Quality engineer (supply)

Do you want to join the creation and development of the new manufacturing for our Continence Care segment within Coloplast?

Be a service partner for/and support the production process, from a quality function, to produce the products our users’ needs in the quality needed?

Then look at this position: Supplier Quality Engineer

Here you will play a key role in the quality of the products produced as a partner in the release process of raw materials and troubleshooting for supplier related topics. You will play a pivotal role in ensuring the success of our roll-out plan as the quality of raw materials and close supplier collaboration is a key component and the gate keeper for sending materials to production, at our new site. Furthermore, the quality of our production starts with the incoming materials, which we verify and ensure the quality of our raw materials and therefore for our users.

An unexhausted list of what You will Do:

• Support and promote the quality culture for the whole site
• Lead, execute and document quality activities on site in connection with suppliers
• Be the approver of documentation related to raw materials and products on site
• Manage the complaint handling processes with suppliers
• Support production – Partner towards production for changes, troubleshooting, deviations and improvement activities
• Ensure and facilitate/execute failure analysis and corrective/preventive action in connection with deviations
• Review and support improvements of specifications
• Participation in root cause analysis regarding raw materials and suppliers
• Communicate with the production, supply chain and the suppliers
• Be the first line of communication for suppliers for the site

Your Qualifications:

• Academic background: A relevant academic background (B.Sc. or higher).
• Experience: Minimum 2 years as a Supplier Quality Engineer or similar within a production environment, preferably Medical device production
• Solid understanding within the field of Quality in relation to production i.e. GDP and GMP etc. (Quality Assurance experience is a plus)
• Knowledge of certificates, documentation from quality point of view, contracts, QC, SCAR, CAPA, etc.
• Project knowledge and experience
• Production knowledge – Value chain understanding
• Business understanding: Holistic understanding of End-To-End production
• Language Proficiency: Fluent in spoken and written English (other languages are a plus).

Timing:

Workplace will be Felgueiras in Portugal

The workplace will in Felgueiras, Portugal at our site and introductions/trainings at our other sites in Hungary and Denmark. The travel program will be defined together with the manager.

Pursuing an ambitious growth agenda, Coloplast develops and markets products and services that make life easier for people with intimate healthcare needs. Employing about 16,000 people and with products available in more than 143 countries, we are one of the world´s leading medical device companies. We are constantly growing our business and always looking for new ways to move forward – we explore, learn and look for new ways of doing things.

Coloplast is committed to being an inclusive organization, where people bring their differences to work each day, fulfil their potential and have a strong sense of belonging because – and not despite – of their differences. We therefore encourage all qualified candidates to apply regardless of gender, age, race, nationality, ethnicity, sexual orientation, religious belief or physical ability.

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