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Coloplast at the Mørdrup site in Denmark is seeking a Laboratory Technician for the Quality Assurance Lifecycle Laboratory on a 12-month cover position. You will join a team of 10 technicians and 2 test method specialists supporting production, development, investigations and test method activities.
You will perform tests, document results, and contribute to quality investigations while collaborating with QA, R&D and Operations in a dynamic environment.
Location: Espergærde, DK
Job Family: Quality Assurance
Imagine if the quality of both new and existing Coloplast products started with... you.
“This is an opportunity to work with quality assurance at different stages of a product’s lifecycle. Your laboratory work and attention to detail will contribute directly to ensuring high-quality products for people with intimate healthcare needs,” says Lotte Stoklund, Team Manager, QA Lifecycle Laboratory.
At our Coloplast Mørdrup site, you will join the Quality Assurance Lifecycle Laboratory. The team consists of 10 laboratory technicians and 2 test method specialists who work closely together to support ongoing production, process development, quality investigations, and test method activities.
You will become part of an engaged and supportive team with a strong team spirit and a valuable mix of practical laboratory experience and specialist knowledge. We place great emphasis on engagement, collaboration, and creating a working environment where people feel included, support one another, and share knowledge across tasks and responsibilities. In our daily work, we collaborate closely with colleagues across Quality Assurance, Research and Development, and Operations, and we value curiosity, flexibility, and a continuous improvement mindset.
As a Laboratory Technician, you will perform laboratory testing and ensure that results and documentation meet applicable quality requirements. Your tasks will vary depending on production needs, development activities, investigations, and project priorities.
Your primary responsibilities will include:
You can expect a role with both routine and non-routine laboratory activities. You will have the opportunity to build a broad network across the organization and gain experience with quality assurance at several stages of a product’s lifecycle.
To succeed in this position, you work carefully and systematically and understand the importance of accurate documentation and data integrity. You take responsibility for your tasks, follow established procedures, and communicate clearly if you identify unexpected results, quality risks or challenges. You enjoy working both independently and as part of a team. As priorities may change depending on production and project needs, you are flexible and able to organize your work accordingly.
We imagine that you:
Experience from the medical device industry, working under Good Manufacturing Practice (GMP) requirements, or using a Laboratory Information Management System (LIMS) is an advantage, but not a requirement.
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.
Coloplast Group - Holtedam 1 - Humlebaek - DK 3050 - Denmark