ABOUT YOU

We are looking for an experienced candidate with excellent communication, stakeholder management and collaboration skills and a high degree of business acumen.
You understand that key contributing factors to success are collaboration - and at the same time deliver high quality and timely solutions and deliverables. You are well structured and methodological and know when to execute and delegate, and how to make right prioritisations.
To be truly successful in this position you will take the lead to develop and execute the agreed supplier/category strategy that supports the overall Convatec strategy and business need. You have a high level of language skills in Danish and English, both written and verbal.

QUALIFICATIONS

• BS/BA degree in medical engineering or life sciences
• Minimum 3 years’ experience in the medical device industry
• Supplier Quality experience
• Experience in internal and supplier related CAPA/NC
• Knowledge and implementation of effective quality control for manufacturing and supply chain operations, particularly in supplier evaluation, selection, auditing, and supplier management programs
• Ability to negotiate and partner with internal and external customers to enhance operational effectiveness
• Knowledge of GxP and relative standards for manufacturing environments
• Ability to work with people / teams in a complex, changing environment, to deliver value-added results to the business
• Knowledge of regulatory requirements that affect the medical device manufacturing business and put policies and systems in place to achieve conformance: QSR Part 820, ISO 13485, MDD 93/42, ISO 9001, GMP Parts 201 and 211, EU MDR

ABOUT US

We offer you a position in a dynamic and global company where the days are never the same. Convatec will provide you with challenges and development opportunities and the chance to influence your own role from day one. You will be a part of a great community where we all help and support each other – while continuously building on our competences and network.
Interviews will be conducted continuously, so we encourage you to submit your application (in English) as soon possible. In case of questions to the position, please contact Quality Engineering Manager, Rikke Eiland +45 31 64 83 65. We look forward to hear from you!
You do not need to attach a cover letter to your application, but please include your motivation applying for the job in your CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.

You will be responsible for maintaining and enhancing our Supplier Quality area. Your will work in close collaboration with Category Managers, Mould Team, R&D, QA and Operations in Denmark and Mexico. We can offer you a central role in an exciting company in constant growth, where you will have a great influence on the projects and processes of which you are a part.

Other responsibilities in this role include:

• 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
• Support and lead where appropriate, supplier selection, evaluation and approval
• Participate in Supplier Audits for new and existing suppliers
• Handle Non-conformances and corrective actions when escalated
• Build strong relationships with customers, suppliers, stakeholders and support groups worldwide to meet the demands of a changing business environment
• Demonstrate expert technical knowledge and principles in relation to medical devices

You will report to Quality Engineering Manager and the work location is in Osted, Denmark, south of Roskilde. We offer a hybrid office environment, with some possibility to work from the office in Søborg or from home, as it fits the projects you are a part of. You can expect approx. 20-25 travel days annually.
This position is based in Denmark.