SIRE Life Sciences®

QA Officer

Location: Belgium
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 Vlaams-Brabant Belgium.

The Company

The Quality Assurance department ensures that the products are manufactured, stored and packaged in accordance with cGMP.

Role Description

Next to ensuring that the products are manufactured, stored and packaged, you will also support the development of GMP training packages and (if needed) delivery of the training. You will continuously improve QA and Compliance systems, strengthen the quality awareness and investigate quality under the guidence of the reporting manager. As a QA Officer you will reporting to the Head of Quality;

Responsibilities

• Deviations , Out Of Specs, Change Control and CAPA's;
• Documentation and batch record reviewing:
• Maintain the calibration program and monitoring;
• Documentation System Management: Traceability, Official document distribution, maintain training files and update the archives;
• Continuous improvement;
• Inspections & internal audits;
• Collaborating with different relevant departments to resolve compliance matters and to ensure timely closure of quality related actions;

Requirements

Minimum:
• Several years experience in a QA position in a GMP regulated environment;
• Master degree in Sciences;
• Excellent French and English (written and spoken);

Job Specific:
• Good knowledge of GMP in a regulated environment;
• Accurate & attention to detail;
• Interpersonal skills;
• Knowledge of MS office (Word, Excel, PowerPoint) and TrackWise® is a plus;
• Problem & Issue solving skills, root cause analysis;
• Flexible / adaptive / independent / multitasking;




Specific competences required:
• Good knowledge of cGMP in a regulated environment (ICH Guidelines)
• Excellent accuracy and attention to detail
• Excellent interpersonal skills
• Working knowledge of MS office packages (Word, Excel, Power Point) and TrackWise® System is in asset
• Strong problems solving skills, issue resolution and root cause analysis
• Highly Flexible and Adaptable. Able to work independently in a fast paced multitasking environment

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rutger Koning.
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SIRE Life Sciences®

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