QC Project Specialist
Location: NetherlandsSIRE 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 Zuid-Holland Netherlands.
Our client is a Pharmaceutical company in Leiden.
ROLE DESCRIPTION
- You are responsible for handling complex deviations for the entire QC Department
- You are responsible for setting the standards for Quality within the lab and handle deviations, change control and lead improvement projects
- During audits and inspections by internal or external stakeholders you will guarantee the information stream for the QA department and serve as QC subject matter expert for GLP/GMP related questions
RESPONSIBILITIES
Support QC Lab with:
- Complex Deviations
- LIMS Management
- Equipment Life Cycle Management
- Sample Management
- Change Control
REQUIREMENTS
- Academic degree
- Fluency in English (Dutch Advantageous)
- Experience in Laboratory and GMP Environment
- Excellent Communicative skills
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.
