Senior Quality Manager
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, Biotechnology and Healthcare organisation, based in Noord-Brabant Netherlands.
- Ensure that all the aspects of the business concerning the projects are in line with the quality strategy of the company
- Perform inspections, observations and audits
- CAPA and deviation management
- Provide MPS training
- Scrutinize compliance and guide concerning activities in the quality areas
- 5-10 years of experience in a quality role in a pharmaceutical environment
- Extensive knowledge of LSS (black belt) and GMP
- Experience with regulatory guidelines concerning manufacturing practices
- Autonomous problem solving, management and complex decision-making skills
The Company
Our client is a professional Biotechnology, Healthcare and Pharmaceutical organization, based in Noord-Brabant Netherlands. This global organization is a market leader in healthcare with a focus on prescription medicine. Their goal is to invest in deciphering the world’s medical dilemma’s. They value diversity in a multinational, talented environment in which they help their employees grow.Role Description
The quality departments collaborate actively within the organization and within your division you will be reporting to the quality director. You will closely examine the improvement in your department and lead LSS projects. You will make sure LSS improvements are actually happening.Responsibilities
- Employ LSS tools for improving procedures and processes in the quality department- Ensure that all the aspects of the business concerning the projects are in line with the quality strategy of the company
- Perform inspections, observations and audits
- CAPA and deviation management
- Provide MPS training
- Scrutinize compliance and guide concerning activities in the quality areas
Requirements
- BSc in Biotechnology or related field- 5-10 years of experience in a quality role in a pharmaceutical environment
- Extensive knowledge of LSS (black belt) and GMP
- Experience with regulatory guidelines concerning manufacturing practices
- Autonomous problem solving, management and complex decision-making skills
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