Quality Officer
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 Brabant Wallon Belgium.
- Provide support to Qualified Person
- Coordinate and follow up on quality incidents, deviations and customer complaints.
- Define and follow up on corrective actions and preventive actions (CAPA).
- Coordinate and follow up on any relevant Change Control.
- Stimulate continuous improvement of the QMS and participate in the writing of Quality documents.
- Perform internal audits
- Perform external supplier and subcontractor audits (offsite).
- Assists in customer quality audits.
- 3-5 years’ experience in QA function, preferably also in Auditing
- French and English; any additional language is an asset..
- Excellent communication and intercultural skills.
- Team worker and team spirit.
- Customer oriented.
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.
The Company
Interesting global pharmaceutical company dedicated to deliver medicines quickly to patients in need with innovative solutions.Role Description
In this role you will be responsible for QA activities in a broad sense. You will support the QA Director and QP.Responsibilities
- Review and approve Batch records- Provide support to Qualified Person
- Coordinate and follow up on quality incidents, deviations and customer complaints.
- Define and follow up on corrective actions and preventive actions (CAPA).
- Coordinate and follow up on any relevant Change Control.
- Stimulate continuous improvement of the QMS and participate in the writing of Quality documents.
- Perform internal audits
- Perform external supplier and subcontractor audits (offsite).
- Assists in customer quality audits.
Requirements
- BSc. or MSc. in Life Sciences- 3-5 years’ experience in QA function, preferably also in Auditing
- French and English; any additional language is an asset..
- Excellent communication and intercultural skills.
- Team worker and team spirit.
- Customer oriented.
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.
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