QA Consultant
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 Biotechnology and Pharmaceutical organization, based in Baden-Württemberg Germany.
Our client is a Pharmaceutical and Medical Device company in Freiburg
ROLE DESCRIPTION
- Responsible for Review of QA Documents
RESPONSIBILITIES
- Review of GMP documents such as SOP's
- Negotiate deficiencies in GMP documents with management
- Contact person for QA questions on eDMS
- Write GMP documents
- Evaluation of QA tools
- Training and coaching of employees
REQUIREMENTS
- B.Sc. / M.Sc. or relevant Life Science Degree (chemistry, biology, pharmacy or related)
- Fluency in English
- GMP Knowledge
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.
