Qualified Person / Pharma / Temporary / Noord - Holland
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.
Are you a person who always driving by an urge to get the best results and do you have experience within the GMP of the pharmaceutical industry? Then keep on reading!
The function is very diverse and your days will never be boring. All these tasks you will perform in a team of professionals with affinity for the pharmaceutical industry.
- The implementation of the quality regulations
- Monitoring and reviewing the execution of the quality regulations
- Operating the quality systems
- Streamlining the validation of the processes
- Internal audits, complaint management and deviations
- Has a PharmaD or BSc in pharmacy
- Has at least 2 years experience as Qualified Person
- Has good knowledge of current Quality regulations
- Speaks both English and Dutch fluently
- Is a team player and eager to learn
- Having experience as an QP is a plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ria Bos.
The Company
This market leader aims to maintain her leading position within the pharmaceutical industry by staying focused and being committed. Their goal is to improve the lives of worldwide patients. They do this by always striving for the best result and offering innovative solutions. Our client attaches great value to keep developing and improving themselves. This vision also reflects on their employees, which are eager to learn and driven by ambition.Are you a person who always driving by an urge to get the best results and do you have experience within the GMP of the pharmaceutical industry? Then keep on reading!
Role Description
For our quality department we are looking for a Qualified Person for a period of 5 - 7 months. As a Qualified Person your most important task will be to monitor the implementation of the quality regulations. Besides you will also be responsible for the execution and review of the quality regulations. You will work with different quality systems which have to meet the current GMP standards. In addition the job includes the implementation of internal audits, deviations, validation of the processes and complaint management.The function is very diverse and your days will never be boring. All these tasks you will perform in a team of professionals with affinity for the pharmaceutical industry.
Responsibilities
You are responsible for:- The implementation of the quality regulations
- Monitoring and reviewing the execution of the quality regulations
- Operating the quality systems
- Streamlining the validation of the processes
- Internal audits, complaint management and deviations
Requirements
We are looking for someone who:- Has a PharmaD or BSc in pharmacy
- Has at least 2 years experience as Qualified Person
- Has good knowledge of current Quality regulations
- Speaks both English and Dutch fluently
- Is a team player and eager to learn
- Having experience as an QP is a plus
Other information
We offer you an inspiring and educational working environment and the possibility to make a difference.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ria Bos.
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