QA 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 Pharmaceutical organization, based in Noord-Brabant Netherlands.
This company discovers, develops and produces new innovative human therapeutics that improve the life expectancy of humanity.
ROLE DESCRIPTION
In this position you are responsible for oversight on equipment, automation and IS validation. The qualified staff of the company has oversight on the QA validation activities. You make sure the regulatory requirements are met and you maintain close contact with the Quality systems of the company.
RESPONSIBILITIES
You are providing guidance and direction to Quality, Production and Supply Chain staff in regards to compliance with quality policies and procedures. Keeps quality oversight on validation strategy and deliverables for specific projects.
REQUIREMENTS
- Master degree
- 10 years experience in a GMP environment
- 5 years relevant experience in Equipment and Automation Validation
- Knowledge of Non Conformances and CAPA's
- Fluent in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Leon Moonen.
