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Analyst (Chemical lab)
Eingestellt von Radiant systems Inc
Gesuchte Skills: Engineering, Support, Engineer
Projektbeschreibung
Job Title: Analyst(Chemical lab)
Job Type: Contract
Location: Puurs, Belgium
Languages: English and Dutch
Scope of work:
The independent execution and reporting of one or more routine chemical tests according to the legal and current cGMP guidelines within the chemical QC lab:
After a training period, you perform independent lab analyzes. These analyzes are performed to support product release, complaint handling and/or projects in product development and validation. Based on your experience in chromatographic analyzes (and EMPOWER) and/or bio-analytical tests (ELISA) within a GMP environment, you can quickly be deployed.
You ensure that the documentation of the analyzes carried out is correct and in accordance with cGPM guidelines.
You ensure that your knowledge about cGMP, procedures and safety stays up-to-date.
In close cooperation with the project engineering and quality engineer, you contribute to troubleshooting and a preventive approach
As part of a team, you are jointly responsible for achieving preconceived objectives regarding productivity, quality and safety Requirements:
You preferably have a professional bachelor in pharmaceutical sciences, chemistry, clinical, pharmaceutical or biological laboratory technology
You have practical experience with lab analyzes: non-chromatographic (analysis of raw materials, SDS, ELISA ...) and/or chromatographic tests (HPLC, UPLC, GC ...)
You work meticulously and place high priority on quality
You have a strong affinity for conducting routine analyzes
You have a strong interest to work in a GMP environment. Experience within a GMP is a strong asset.
You have a high problem-solving capacity
You think safety is very important
You are flexible and have a "can-do" mentality
You have a good knowledge of Dutch and English
You can work with PC software applications (MS Office, LIMS)
Job Type: Contract
Location: Puurs, Belgium
Languages: English and Dutch
Scope of work:
The independent execution and reporting of one or more routine chemical tests according to the legal and current cGMP guidelines within the chemical QC lab:
After a training period, you perform independent lab analyzes. These analyzes are performed to support product release, complaint handling and/or projects in product development and validation. Based on your experience in chromatographic analyzes (and EMPOWER) and/or bio-analytical tests (ELISA) within a GMP environment, you can quickly be deployed.
You ensure that the documentation of the analyzes carried out is correct and in accordance with cGPM guidelines.
You ensure that your knowledge about cGMP, procedures and safety stays up-to-date.
In close cooperation with the project engineering and quality engineer, you contribute to troubleshooting and a preventive approach
As part of a team, you are jointly responsible for achieving preconceived objectives regarding productivity, quality and safety Requirements:
You preferably have a professional bachelor in pharmaceutical sciences, chemistry, clinical, pharmaceutical or biological laboratory technology
You have practical experience with lab analyzes: non-chromatographic (analysis of raw materials, SDS, ELISA ...) and/or chromatographic tests (HPLC, UPLC, GC ...)
You work meticulously and place high priority on quality
You have a strong affinity for conducting routine analyzes
You have a strong interest to work in a GMP environment. Experience within a GMP is a strong asset.
You have a high problem-solving capacity
You think safety is very important
You are flexible and have a "can-do" mentality
You have a good knowledge of Dutch and English
You can work with PC software applications (MS Office, LIMS)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges