QAO / Pharma / Permanent / Region North-Brabant / GMP
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 Netherlands.
A completed HBO study in a quality direction in the pharmaceutical industry.
Knowledge of quality management systems.
At least 2 years of relevant work experience within (preferably) the pharmaceutical industry.
Excellent knowledge of the Dutch and English language (word en written).
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.
The Company
Our client is an innovative CDMO with a focus on the development and cGMP production of novel active pharmaceutical ingredients and nanomedicines.Role Description
You will be responsible for managing the Quality Management Systems. It will be your job to ensure that the actions meet the GMP requirements. In addition, whether the products that have been put on the market are in line with the registrations of the regulatory authorities. As a quality assurance officer you are responsible for part of the quality supervision. Therefore you will report to the Quality Manager.Responsibilities
Your responsibilities consist off Managing the Quality Management Systems, give support with the implementation and implementation of the new global quality systems, prepare and / or following specific quality-related meetings and follow up and / or turn off QMS document adjustments.Requirements
Our client have a few requirements, these are:A completed HBO study in a quality direction in the pharmaceutical industry.
Knowledge of quality management systems.
At least 2 years of relevant work experience within (preferably) the pharmaceutical industry.
Excellent knowledge of the Dutch and English language (word en written).
Other information
Our client understand the needs of their employees, this means that you will be provide of excellent primary and secondary employment conditions depending on experience and training. Also you will work in an international environment with growth opportunities.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.
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