Manager Pharmaceutical Product Qualification
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Biotechnology and Pharmaceutical organization, based in Noord-Holland Netherlands.
The company provides medicines and medical goods to healthcare organisations worldwide, at the best price possible. In this way the healthcare providers have access to quality products at a fair price.
ROLE DESCRIPTION
The Manager Pharmaceutical Product Qualification ensures that the quality of all pharmaceutical products supplied by client is compliant with their quality policy, documents evidence of this, and drives the approval procedure. In addition, he/she ensures that relevant product information is available to customers and other departments. The Manager Pharmaceutical Product Qualification reports to the Manager Quality Affairs and manages several Quality Assurance Officers.
RESPONSIBILITIES
- Qualify pharmaceutical products
- Assess product dossier and samples
- Review and approve product specifications, final leaflet texts, label and packing specifications
- Manage the archiving and distribution of quality documents such as specifications, protocols, methods of analysis, manufacturing licences and GMP certificates
-Provide technical training to other departments
- Contribute to the improvement of business processes and the development of policies and standards
- Reporting lines
REQUIREMENTS
- Master of Science in a relevant field such as pharmacy, biopharmaceutics, chemistry, biology or physiology
- Minimum 3 years of relevant working experience in quality assurance of pharmaceuticals
- Excellent verbal and written communication skills in English
- Experience in managing other people
- Strong problem solving skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
