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 and Biotechnology organisation, based in Brussels Hoofdstedelijk Gewest Belgium.
- Streamlining processes across the laboratories
- Performing internal and external audits
- Making sure that all personnel has the appropriate training in regards to the QMS
- Ensuring and building supportive working relationships concerning quality throughout the organization
- Managing the implementation of CAPA’s across the laboratories
- Knowledge of Lean Six Sigma
- Several years of experience in a regulated pharmaceutical, clinical research and/or lab environment
- Fluent in French and English; Dutch is an asset
- Flexible, punctual and excellent communication skills
The Company
Our client is a professional Biotechnology and Pharmaceutical organization, based in Brussel Belgium. They are a rapidly expanding company with a focus on clinical trials in the pharmaceutical industry. They are on a mission to provide all the support necessary for analytical analyses. Implementing new quality standards require personnel with the right mindset, and this is where you come into play.Role Description
You will be reporting to the managing director and will ensure a strong quality and compliance structure. You will be responsible for separate laboratories in which you will manage the development and maintenance of the Quality Management System. At first, it will not be people managing but the role is prone to grow into that.Responsibilities
- Coordinating and managing the QMS and connected procedures- Streamlining processes across the laboratories
- Performing internal and external audits
- Making sure that all personnel has the appropriate training in regards to the QMS
- Ensuring and building supportive working relationships concerning quality throughout the organization
- Managing the implementation of CAPA’s across the laboratories
Requirements
- MSc. in life science related field- Knowledge of Lean Six Sigma
- Several years of experience in a regulated pharmaceutical, clinical research and/or lab environment
- Fluent in French and English; Dutch is an asset
- Flexible, punctual and excellent communication skills
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