SIRE® 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 Zuid-Holland Netherlands.

The Company

They are an multinational organization who focus especially on services in pharmaceutical development of products that are focused on curing different diseases. A company that belong to the top in pharmaceutical in the world.

Role Description

Your will be responsible for ensuring that the QMS are compliance to the regulations. These systems and procedures need to be optimized so there will be an continuous quality improvement in line with the strategy and mission.

Responsibilities

- Lead projects of quality improvement
- Utilizing techniques and statistical tools and support the activities of engineering in process
- Data testing, analyzing for improvement, QMS data
- Validation reviewing and ensure software validation
- Leading teams with CAPA’s/audits
- Oversee detailed process development

Requirements

- MSc. or BSc in Engineering or science
- 3-5 or more years of experience in a medium or large scale matrix organization in Pharmaceuticals
- Knowledge of software and process validation and of Statistics
- Knowledge of Crystal Reports programming