SIRE® 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, Biotechnology and Clinical Research organisation, based in Noord-Brabant Netherlands.
Our client is a reputed contract partner providing drug substance and drug product development, manufacturing, logistics and bioanalytical services to pharmaceutical customers globally.
Our client is searching for a Sr. Quality Assurance Officer for their business unit specialized in chemical process and analytical development.
If you are ambitious, it is worth reading the hole profile!
As an Sr. Quality Assurance Officer you need to ensure the GMP manufacturing activities on the shop floor and in the analytical laboratory, are executed in accordance with cGMP requirements.
Also you need to adheres if the Quality Management System (QMS), is consistent with existing corporate & regulatory guidelines and contributes to continuous improvement through leveraging the QMS architecture, assuring product quality and safety.
Knowledge en experience with a great personality, are the right elements for the job.
As Sr. Quality Assurance Officer you will give GMP advice, document review and approval, deviation handling, overall advising, facilitating and supporting all phases of manufacturing / analytical batch documentation development.
You will also review and approve GMP documentation, Handling Deviations and Change Controls, Releasing or rejecting finished products based on quality review, Executing and improving the QMS, Evaluating the performance of the Quality Management systems by means of internal audits, Initiating and supporting CAPA’s,
You need to have :
And you need to be :
Our client offers you a challenging job in an international environment within one of the most innovative industry branches : the pharmaceutical industry.
Our client has an open culture!
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.