QA Coordinator GMP, Development and Supplier
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 Rheinland-Pfalz Germany.
Our client is an international cooperating Biotech company with an impressive product pipeline and well known customers in the pharmaceutical industry.
ROLE DESCRIPTION
In this function you will help to develop production techniques for RNA-medicines within the GMP guidelines. Furthermore you will help to transfer production methods of RNA carrying nanoparticles to a partner of our client.
RESPONSIBILITIES
- Transfer of production in accordance to quality (especially GMP) standards
- Coordinating external suppliers and taking care that quality standards are met
- Explore new technologies for the production liposomes and RNA Nanoparticles
REQUIREMENTS
- Degree in pharmacy, pharmaceutical technology or natural sciences
- Deep knowledge of GMP standards
- Knowledge in Drug Delivery, preferred in DNA/RNA delivery
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Robin Krems.
