Quality Assurance Manager
Location: BelgiumSIRE® 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 Vlaams-Brabant Belgium.
Support in releasing secondary packaged medicines under the the clients supply chain manufacturer authorizations granted for medicinal products for human and veterinary use in accordance with applicable regulations. Maintaining and improving the quality standards, resulting in compliance with legal and customer requirements. You will lead a team of 6/7 and you are responsible for giving advise in GDP and GMP regulations.
- Maintenance and improvement of Quality Management Systems
- Batch Release
- KPI audits
- Change Control, CAPA's and selling quality to the operational manager
- Contactperson clients
• Minimum 3 years experience in the pharmaceutical sector, which at least 2 years in a QA role.
• Experience in the field of auditing and supervision of inspections.
• Performance Indicators (KPI's)
Competency
• Strong management skills and a strong personality
• Representative appearance and behavior
• Analytical, process-oriented and well organized
• Steadfast
The Company
Our client is a professional Pharmaceutical organization, based in Brabant Flamand Belgium. A global leader in the logistics and a global healthcare leader with a strong focus on the research, development and are patient-orientated.Role Description
Ensuring that the site meets the conditions of the QMS. You are responsible together with the RP to manage and implement tools, programs, certificates etcetera to achieve this.Support in releasing secondary packaged medicines under the the clients supply chain manufacturer authorizations granted for medicinal products for human and veterinary use in accordance with applicable regulations. Maintaining and improving the quality standards, resulting in compliance with legal and customer requirements. You will lead a team of 6/7 and you are responsible for giving advise in GDP and GMP regulations.
Responsibilities
- Managing personnel- Maintenance and improvement of Quality Management Systems
- Batch Release
- KPI audits
- Change Control, CAPA's and selling quality to the operational manager
- Contactperson clients
Requirements
• Graduated (BSc.) in Pharmaceutical, Biological or Chemical study• Minimum 3 years experience in the pharmaceutical sector, which at least 2 years in a QA role.
• Experience in the field of auditing and supervision of inspections.
• Performance Indicators (KPI's)
Competency
• Strong management skills and a strong personality
• Representative appearance and behavior
• Analytical, process-oriented and well organized
• Steadfast
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