Freelance QA Validation Specialist
Location: BelgiumSIRE 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 Antwerpen Belgium.
The company is a contract manufacturing organization that provides production and proces development services for pharmaceutical companies worldwide.
ROLE DESCRIPTION
In this role you will be responsible for the validation of production processes and reports in order to ensure GMP compliance. Therefore you will need to interpret excisting production processes and data to ensure that they comply with GMP standards, client requirements and patient safety. The duration of the project is at least 6 months.
RESPONSIBILITIES
- Project management for new and existing products
- Establish validation plans and review validation plans in case of changes in the process
- Review documentation in regards to changes and deviations in the production processes
- Root cause analysis in order to determine corrective actions
- External audit and inspections by authorities
REQUIREMENTS
- Master in Science in a life science related field
- Minimum of 5 years of experience in the pharmaceutical industry
- Good understanding of pharmaceutical regulations
- Good knowledge of production processes and GMP
- Fluent in English and preferably also Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Kimberley Rijnbeek.
