Ambitious QA/QC Specialist / Permanent / Pharma Start up / Gelderland
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 Gelderland Netherlands.
- Validation tasks relating to the clean room and the lab;
- Optimalisation of the SOPs;
- Deviations, CAPAs and change controls.
- GMP & GDP knowledge or experience;
- Experience in Quality
- An entrepeneurial mindset;
- A hands-on mentality and wanting to contribute to the company on a strategic level.
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 rapidly growing start up in the Brecht region (Antwerp) that is looking for QA/QC specialists with a strong entrepeneurial mindset. This is a great opportunity for professionals who aren't afraid of responsibility, want to think on a strategic level for the company and really contribute to the overall succes of this growing organisation. This small but rapidly growing organisation is responsible for the distribution of APIs.Role Description
This is still a young and developing company, and your experience will determine what kind of responsibilities you can pick up in the organisation. You will be part of a young and dynamic team, which will give you the space and opportunity to grow, learn and give your own input. Together you will shape the course of this company and get to be part of the organisation (both strategically and financially). Above all this job means freedom, flexibility and independence.Responsibilities
- Batch record review and - if you are a certified QP - batch release;- Validation tasks relating to the clean room and the lab;
- Optimalisation of the SOPs;
- Deviations, CAPAs and change controls.
Requirements
- MSc. Life Sciences;- GMP & GDP knowledge or experience;
- Experience in Quality
- An entrepeneurial mindset;
- A hands-on mentality and wanting to contribute to the company on a strategic level.
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.
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