Senior Quality Assurance Manager (contract / freelance / zzp / interim)
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-Holland Netherlands.
The company has a long history and has established itself as a market leader in a variety of indications.
In this role, you will be providing support to the Quality Systems and GMP / GDP compliance functions within the Quality department. You will set up and implement the quality systems for Europe, and translate this into concrete actionables and support the Qualified Person (QP) on site.
This role will suit an entrepreneurial individual who is looking for a role where they can build out a Quality department from scratch.
A strong background in small molecule GMP (SMOL's) is required for this position.
In exchange, you will be offered a challenging and dynamic project where you are given the freedom to build up a QA department.
A highly competitive day rate is available.
* Support other functions such as commercial, regulatory and supply chain
* Generate, review and approve GMP / GDP - SOPs, CAPA's, deviation investigations etc.
* Implement, maintain and support GxP European quality systems - CA inspections, global QMS projects
* Continuous Improvement
* Demonstrable track-record in setting up Quality Management Systems (QMS)
* Experience in GxP and GMP / GDP / GMDP compliance
* Minimally 5 years of experience in Quality Assurance (QA) within the Pharmaceutical industry
* Based in the Netherlands with the ability to work from the North-Holland office
* Fluency in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
Our client is an established and innovative global pharmaceutical company who manufactures and markets a wide range of established, as well as innovative small molecule drugs, including anti-viral, antibiotic and generic.The company has a long history and has established itself as a market leader in a variety of indications.
Role Description
They are presently moving their European HQ to the Netherlands, and as such, are looking for a Senior Quality Manager (freelance, zzp, interim, consultant) to set up shop.In this role, you will be providing support to the Quality Systems and GMP / GDP compliance functions within the Quality department. You will set up and implement the quality systems for Europe, and translate this into concrete actionables and support the Qualified Person (QP) on site.
This role will suit an entrepreneurial individual who is looking for a role where they can build out a Quality department from scratch.
A strong background in small molecule GMP (SMOL's) is required for this position.
In exchange, you will be offered a challenging and dynamic project where you are given the freedom to build up a QA department.
A highly competitive day rate is available.
Responsibilities
* GMP / GDP Compliance support - including internal and external auditing, GMP / DP deviations and CAPA's etc.* Support other functions such as commercial, regulatory and supply chain
* Generate, review and approve GMP / GDP - SOPs, CAPA's, deviation investigations etc.
* Implement, maintain and support GxP European quality systems - CA inspections, global QMS projects
* Continuous Improvement
Requirements
* Strong background in small molecules (SMOL's) / chemistry* Demonstrable track-record in setting up Quality Management Systems (QMS)
* Experience in GxP and GMP / GDP / GMDP compliance
* Minimally 5 years of experience in Quality Assurance (QA) within the Pharmaceutical industry
Other information
* 3 Month full-time availability (extension possible)* Based in the Netherlands with the ability to work from the North-Holland office
* Fluency in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
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