Quality Management Coordinator
Location: GermanySIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Healthcare and Medical Devices organization, based in Berlin Germany.
Our client is a Medical Device company specialized in developing orthopedic solutions for supporting patient who are recovering from a trauma or surgery. Closely working with experienced doctors they work on a high level quality to ensure people to get back to their normal lives and make it dynamic again.
ROLE DESCRIPTION
The client is looking for a quality coordinator (m/f) that will be responsible for handling the complaints division and managing the complaints database as well (CAQ). The client is located in the Berlin region and operates on a global level in the field of medical technology.
RESPONSIBILITIES
-You will be responsible for managing the quality in the production and development of the medical devices
-You will have to comply to quality standards, for example ISO 13485 and CFR 820
-You will be supervising the CAPA processes and comply with licensing requirements
-You will be supporting the project team and the CIP process together with the CAPA entities
-You will also be informing and training employees in the complaints processes
REQUIREMENTS
-A completed degree in computer science, economics or mathematics
-3-5 years of working experience in the field of quality management in medical technology
-Knowledge and working experience with ISO 13485, 93/42 / EEC, 21CFR820, ISO 14971, IEC60601-1, in accordance with the relevant laws, standards and guidelines of medical technology
-Experience with coordinating and project planning as well as strong leadership skills
-High level of English writing together with verbal skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Klaas-Jan van Duin.
