Specialist QA
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 Noord-Brabant Netherlands.
A multinational company in Biotechnology.
ROLE DESCRIPTION
The main tasks are to have an overview of the Quality policies and procedures and support the production staff to be compliance with these matters. You will assist and lead in investigations and handle non conformances and CAPA’s. You will participate in ABR projects and you will be a part of performing risk analysis. In this GMP environment you will perform GMP compliance checks and assist in GMP training activities for production- and QA staff.
RESPONSIBILITIES
- Train employees in GMP activities
- Change control handling
- Approve and review SOP’s
- Participate in different projects
REQUIREMENTS
- MSc. Pharmacist degree or equivalent
- Knowledge of GMP and GDP
- 3-5 years of experience in related area
- Experience with CAPA’s
- Fluent in English and Dutch is preferred
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
