.about convatecpioneering trusted medical solutions to improve the lives we touch: convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care.
with around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring.
our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs.
group revenues in 2024 were over $2 billion.
the company is a constituent of the ftse 100 index (lse:ctec).
to learn more about convatec, please visit the role the process engineer in production is a combination of manufacturing technology with management science and has the scope of engineering practices, aware of management challenges related to production optimizing production processes for the use of resources, scrap reduction, process improvements, poka-yoke design, material and/or product and process changes, production / machinery transfer, process validations and ad-hoc projects.key duties and responsibilitiesin general, the process engineer is key element in the project team and has the authority of suggestingchanges to the product in cooperation with denmark (buid) and the local organization (bud)process engineer in production transfer / product changes.
contact person in mexico when our plant in denmark initiates a production transfer / product change.development of validation documents - analysis of results - preparation of validation reports - coordination of iq - oq -pq - support maintenance documentation - expert on the product to validate - lead projects board mx -dk - update comments ( pqp's) - generate and closing deviations - use of good documentation practices .
perform validation of required processes.product analyzing: ensure machines capacity to achieve daily goals, failures in process and reduction of scrap, rejections in the projects inspections which cause is not known, evaluation and study of movements and times for a better balance in production lines, work closely with related departments in a self-directed team environment to assess opportunities to improve the efficiency, output and manufacturing processes.to follow, develop and acting according to quality assurance system based on iso 13485 and fda cgmp regulations and to comply with the company quality policy.about youas a person, you are structured, well organised, and have a holistic approach to problem-solving.
you actively take the lead on tasks and independently engage with stakeholders to collect relevant information to scope and time activities