QA Process Expert
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 Pharmaceutical organization, based in Bayern Germany.
The represented client is a globally operating pharmaceutical company which has a special focus on research & development. At the moment the company is looking for a new expert in the field of pharmaceutical processes in order to complement the existing department.
ROLE DESCRIPTION
As a QA Process Expert your main responsibility lies in the constant assurance of quality with regard to all processes taking place in the pharmaceutical development. You will validate and analyse current processes in a way that will help you optimise existing processes and create new ones. Further activities that belong to your responsibilities are the management of deviations as well as customer complaints, the qualification of processes, the compliant creation of GMP-documents and the inter-departmental work on QA projects.
RESPONSIBILITIES
- Constant assurance of quality in the area of pharmaceutical development
- Validation, analyses and optimisation of processes
- Deviation management
- Complaint handling
- Process qualification
- Creation of GMP-documents (compliant)
- Inter-departmental work on QA-Projects
REQUIREMENTS
- University degree in a pharmaceutical or scientific field
- Multiple years of experience in a pharmaceutical company with production facilities
- Solid knowledge in GMP regulations
- Fluency in English and German
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Lucas Hüer.
