Quality Assurance Specialist / permanent / Noord-Brabant
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical organisation, based in Noord-Brabant Netherlands.
- Participating in audits and the implementation afterwards
- CAPA's
- Write, review and approve procedures
- +/- 3 years of Quality Assurance experience in a pharmaceutical environment
- Good knowledge of GMP and GDP, GCP is a pre
- Experience with manufacturing or Quality analytical processes is a preferred
- Fluent in English; preferably also in Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
The Company
They are a international company that markets pharmaceutical and biotech products. They invest in research, development and marketing of innovative products that provide solutions for health issues.Role Description
You will be a QA contact for clinical products and are responsible for maintaining effective relationships with other departments on global level. Next to that you will handle product disposition.Responsibilities
More responsibilities are:- Participating in audits and the implementation afterwards
- CAPA's
- Write, review and approve procedures
Requirements
- MSc in life science related field- +/- 3 years of Quality Assurance experience in a pharmaceutical environment
- Good knowledge of GMP and GDP, GCP is a pre
- Experience with manufacturing or Quality analytical processes is a preferred
- Fluent in English; preferably also in Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
