Air Quality Jobs in Bergisch Gladbach

Your roleYou are working in the Clinical Research & Development department which conducts firstinman clinical trials and Phase III proofofconcept studies for our new assets worldwide.You ensure GCP compliance for the clinical trials in collaboration with Quality Assurance to suppo More...

Your roleYou are working in the Clinical Research & Development department which conducts firstinman clinical trials and Phase III proofofconcept studies for our new assets worldwide.You ensure GCP compliance for the clinical trials in collaboration with Quality Assurance to suppo More...

Altenmarkt im Pongau (Austria) or Garching (Germany) Be a part of a transformative journey where your work will directly enhance the efficiency of global supply chain operations. If youre passionate about using data to drive innovation and solve complex problems this role is for you. More...

You will play a pivotal role as a (Senior) C Software Engineer (mfd) for clinical software developing advanced software solutions for our clinical instrument portfolio ensuring seamless hardware integration and upholding the highest standards of quality and compliance in the medi More...

You will play a pivotal role as a (Senior) C Software Engineer (mfd) for clinical software developing advanced software solutions for our clinical instrument portfolio ensuring seamless hardware integration and upholding the highest standards of quality and compliance in the medi More...

Coordinates with technical and regulatory leadership authority the regulatory activities of other RA professionals related to new and approved products on a domestic or international basis.May serve as Global RA program team representative for one or more programs through development More...

Coordinates with technical and regulatory leadership authority the regulatory activities of other RA professionals related to new and approved products on a domestic or international basis.May serve as Global RA program team representative for one or more programs through development More...

In this role you will be responsible for collecting reviewing maintaining and archiving essential regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP) E6 ICH Guidelines and other regulatory guidance documents and Clinical Trials Regulati More...

You are working in the Clinical Research & Development department which conducts firstinman clinical trials and Phase III proofofconcept studies for our new assets worldwide.As Clinical Trial Manager you are responsible for the planning execution  and management of all aspect More...

In this role you will be responsible for collecting reviewing maintaining and archiving essential regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP) E6 ICH Guidelines and other regulatory guidance documents and Clinical Trials Regulati More...

You are working in the Clinical Research & Development department which conducts firstinman clinical trials and Phase III proofofconcept studies for our new assets worldwide.As Clinical Trial Manager you are responsible for the planning execution  and management of all aspect More...

Our customer in the automotive industry has initiated a carveout project to transition an existing unit into an independent company. As part of this project SAP and nonSAP systems will be partially rebuilt adapted and implemented to meet the requirements of the new organization. To su More...

You will contribute to the development and enhancement of our companywide software platform playing a key role in implementing a stateoftheart technology platform for software development in our medical GMP (Good Manufactory Process) and RUO (Research Use Only) instruments. In this ro More...

You will join our team responsible for the postmarket surveillance (PMS) of our clinical products (medical devices in vitro diagnostics and GMP products) and perform organizational and administrative tasks to manage PMS data.    You will be responsible for the mana More...

You will contribute to the development and enhancement of our companywide software platform playing a key role in implementing a stateoftheart technology platform for software development in our medical GMP (Good Manufactory Process) and RUO (Research Use Only) instruments. In this ro More...

You will join our team responsible for the postmarket surveillance (PMS) of our clinical products (medical devices in vitro diagnostics and GMP products) and perform organizational and administrative tasks to manage PMS data.    You will be responsible for the mana More...

You will be responsible for developing and enhancing our software for our cuttingedge analysis devices. This enables researchers to visualize and analyze biological structures and interactions in unprecedented detail particularly in neurology immunology and cancer research. In additio More...

You will be responsible for developing and enhancing our software for our cuttingedge analysis devices. This enables researchers to visualize and analyze biological structures and interactions in unprecedented detail particularly in neurology immunology and cancer research. In additio More...

You will play a pivotal role as a (Senior) C Software Engineer (mfd) for clinical software developing advanced software solutions for our clinical instrument portfolio ensuring seamless hardware integration and upholding the highest standards of quality and compliance in the medi More...

You will play a pivotal role as a (Senior) C Software Engineer (mfd) for clinical software developing advanced software solutions for our clinical instrument portfolio ensuring seamless hardware integration and upholding the highest standards of quality and compliance in the medi More...