QA Manager GCP and GLP
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 Nordrhein-Westfalen Germany.
Our client is a Pharmaceutical company focused on biologics
ROLE DESCRIPTION
Responsible for GMP / GLP / GCP compliance
Responsible for CMC related documents
RESPONSIBILITIES
- Represent Quality in R&D Project teams
- Review documentation in CMC and Quality
- Support clinical activities related to suppliers, registration and consumer test
- Lead change control, deviations and CAPA for the R&D
- Manage the health authorities at R&D Locations
- Lead GMP and related training programs for R&D
REQUIREMENTS
- Life Science degree and at least 5 years of experience
- GMP knowledge and added knowledge of GLP/GCP is advantageous
- Knowledge on how to use IT and Quality systems
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact admin admin.
