Quality Engineer

Quality Engineer (Value Stream) for Convatec Infusion Care

Are you driven by being part of a quality team and helping to optimize and maintain innovative products, specialized in the treatment of chronic diseases such as Diabetes and Parkinson's, improving people's lives? Are you passionate about quality and the collaboration between quality and production to support and improve the quality of our products and do you want to be part of a growing company? Then, you have the opportunity to become part of Convatec as their new Quality Engineer.

Convatec Infusion Care is developing rapidly and is experiencing huge growth. They create new and better products and new ways of working. Including support for their customers and each other. Come on board and become a specialist in continuous improvements to the quality in production, project management and implementation of improvements, and help shape the future of the company and their patients.

About The Role
As a Quality Engineer, you will be part of the Value Stream team with responsibility for supporting and optimizing improvements in production in close collaboration with process engineers and the production team. Coordinating and leading investigations of Root Cause analyses, Gaps analyses, collect data and trend to improve their products and processes. You are offered a central role in an exciting company with great growth, where you will have a great influence on the projects and processes of which you will be a part.

You will report to the Quality Operation Manager and become part of a good quality team, which consists of 5 dedicated specialists with different professional backgrounds.

Your primary place of work is in Osted, south of Roskilde. You will be offered flexibility to work from home, but your primary workplace will be in Osted to support the production.

Your key responsibilities

• Identify potential improvements and implement concrete solutions.

• Coordinate quality/production and projects in collaboration with Value Stream team.

• Support several areas where experience and technical knowledge of the problem can be useful (production, systems, process, components, etc.).

• Coordinate and lead Root Cause investigations with involved team members (maintenance, production, engineering, etc.)

• Trend analyses, process KPIs (PPMs, NCs, etc.) and prepare actions from them.

• Prepare and update documentation in collaboration with the Value stream.

• Effectiveness check and verify implemented solutions.

• Together with colleagues in the production team, ensure a high level of product quality and production efficiency.

To succeed in the role
You are expected to be able to work independently and prepare concrete solutions and improvements. You are systematic with a high-quality mindset and pay attention to detail. You are solution-oriented, flexible and have a pragmatic approach and the ability to create and maintain an overview, and at the same time have several tasks going on at the same time.

You must be comfortable using ISO-standards, FDA, Eudralex vol. 4, etc. and are able to use these as a reference work/guidance to ensure decisions are made based on facts and requirements to the company.

It is important that you want to create results through positive collaboration, where you as a team player contribute to ongoing improvements. You have strong communication skills and can provide constructive feedback as well as guidance and support. You thrive in an informal culture with great degrees of freedom, a great degree of independence with the opportunity to put your own stamp on your daily work and tasks. You have good communication skills in Danish and English, both written and oral. You must have a "can do" attitude and be ready to challenge status quo around the company.

You are comfortable with being challenged on ideas and solutions by stakeholders and will here, based on analytical skills and data, be able to get your solutions safely through process and possible implementation.

You understand that important factors for success are collaboration - and at the same time deliver high quality and timely solutions and deliveries.

You are well structured and know when to execute and delegate and how to set the right priorities.

Qualifications/Education
You have practical experience from production/process optimization and ideally experience with several of the following:

• GMP

• Training

• Hygiene

• Deviation treatment

• CAPA / Root cause investigation

• Clean room

• QA/QC

You are educated as an Engineer, Process Technologist, Pharmacist, Laboratory Technician or similar. Minimum 2 years of experience from the medico-, pharma- or food industry, alternatively other industries with quality/regulatory rules and associated documentation.

About Convatec
You are offered 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 everyone helps and support each other – while continuously building on their competences and network. Interviews will be conducted continuously, so we encourage you to submit your application as soon as possible.

At Convatec, their vision is pioneering trusted medical solutions to improve the lives they touch. They devise, develop, and manufacture innovative products and services that support people with deeply personal and challenging medical conditions, helping to improve care for them and giving them greater confidence, freedom, and mobility.

Convatec, Infusion Care (Unomedical a/s) is a part of a global medical technology business focused on serving people and care givers. They develop and market sterile disposable products for subcutaneous infusion of various medications. Specialized in the treatment of chronic diseases, such as Diabetes Mellitus and Parkinson’s Disease. Their manufacturing facilities in Denmark and Mexico produce more than 100 million infusion sets per year, making them the world leader within this field.

Further information about the company can be found at their website www.b2b.convatec.com or www.convatec.com.

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.

Kilde: Jobnet.dk