QA Officer interim
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 Antwerpen Belgium.
- Lead audits
- Accreditations maintenance
- Review procedures
- Working in a manufacturing environment
- Work together with quality specialists
- Work with GMP, ERR system for example
- 3-5 years of experience in related area
- Knowledge of Microsoft office
- Experience with ISO 9001/ ISO 14001/ PS 9000
- Management skills
- Fluent in English and French is a preferred
The Company
They are an international organization who focus on packaging solutions in the healthcare market. They have a global network with diverse capabilities.Role Description
Currently we are looking for a freelance QA officer. You will be responsible for supporting the QMS maintenance. Administration and documentation of SOP’s and WI’s. You will analyze the internal trends and you are a part in assisting trainings for development. The end date of this project is not yet known, expected 6-8 months.Responsibilities
Your other responsibilities are to optimize planning of manning and resources. You will assist the QA manager in validation activities and maintenance of validation documentation.- Lead audits
- Accreditations maintenance
- Review procedures
- Working in a manufacturing environment
- Work together with quality specialists
- Work with GMP, ERR system for example
Requirements
- BSc. or MSc.- 3-5 years of experience in related area
- Knowledge of Microsoft office
- Experience with ISO 9001/ ISO 14001/ PS 9000
- Management skills
- Fluent in English and French is a preferred
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