Quality Manager
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 Medical Devices organization, based in Hessen Germany.
Within the competitive Medical Device company, this company has been able to develop and get a remarkable share in Class IIb devices.
ROLE DESCRIPTION
The Quality Manager has the responsibility to improve the current Quality Management System introducing new features. Ideally the Quality Manager has a previous training or experience in Green/ Black Six Sigma tools.
While working in Quality, it is expected that the Quality Manager provides expertise in all Quality areas (design control, compliance, risk management...).
In this position communication skills are crucial as the Quality Manager will introduce improvements that can affect other departments. Therefore, it is required that the Quality Manager is able to explain the changes and convince of the importance of implementing them.
Because your strong track record in Quality, you will study ratios, write and supervise Quality documentation, change management, audits, regulatory compliance...
RESPONSIBILITIES
- Improvement of the Quality Management System
- Ensure compliance of ISO 9001, ISO 13485, ISO 14971
- Write and supervise Quality documentation, reporting, development of deadlines
- Develop strategic Quality projects
REQUIREMENTS
- Technical/ Scientific background
- +7 years of relevant experience in Quality (Medical Devices)
- Expert in ISO 9001, ISO 13485, ISO 14971
- German and English language skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
