At the heart of QIAGEN’s business is a vision to make improvements in life possible.
We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe.
Our most valuable asset are our employees more than 5000 in over 35 locations around the world. Our ambition is to ensure we have outstanding and passionate people working in the best teams and we are constantly looking for new talent to join us.
There are few players who have shaped the world of modern science and healthcare as much as QIAGEN, and we have only just started.
If you are looking to advance your career, are seeking new challenges and opportunities, enjoy working in dynamic and international, diverse teams and want to make a real impact on people’s lives, then QIAGEN is where you need to be.
Join us. At QIAGEN, you make a difference every day.
You will be part of a multidisciplinary team within the Life Cycle Management Investigations department. You will be carrying out all tasks in a regulated environment under specific health & safety regulations.
Your responsibilities will comprise :
Writing, conducting, analyzing and documenting Assay / DHF projects (own and / or within Team) according to regulatory standards.
Setting up experiments including : DNA / RNA extraction (manual and / or automated), real-time PCR (manual and / or automated), handling and processing biological samples BSL2, statistical analysis, enzymatic activities.
Supporting manufacturing by monitoring and improving processes of complex systems.
Assisting in the Qualification and Validation of manufacturing equipment and processes within an ISO clean room.
Assisting transfer from R&D to manufacturing of new assays or processes by generating SOPs.
Background : Scientist Degree (desirable PhD); Biomedical, Physics, Biologist or similar.
Multi-disciplinary technical knowledge in some of the following areas : molecular biology, infection diseases, software, optics, microfluidics, heat-management, pneumatics, bioinformatics, multiplex real- timed PCR assays.
Proven organization skills, self-motivated with attention to detail.
Experience in In Vitro Diagnostics (IVD), knowledge of regulatory requirements (IVDD 98 / 79 / EC, ISO 13485, IEC 62304), and experience in Project Management in industrial environment.
Full professional competence in English.
Minimun 3 years of experience in similar position
Good team working ability.
Creative thinking skills.
Curiosity. You wonder how technological products are made or how they work, regardless of how far they may seem from your field of expertise
Hands-on attitude. You enjoy working with prototypes, designing experiments and executing tests.
Organized and methodical.
Able to communicate effectively.