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Junior Chemical Engineer
Eingestellt von Harvey Nash IT Recruitment Belgium
Gesuchte Skills: Engineer, Client
Projektbeschreibung
Our client is a pharamaceutical company and is currently looking for a JUNIOR CHEMICAL ENGINEER to take part to QUALITY CONTROL AND CHARACTERIZATION OF FORMULATIONS. The junior chemical engineer will work for at least 6 months at our client in Walloon Brabant.
Scope of work:
- The physical chemical evaluation of NCEis.
- The characterization of NON-CLINICAL FORMULATIONS of NCE's.
- The development and validation of chromatographic methods for the development and the GLP QUALITY CONTROL of non-clinical formulations of NCEs.
- Apply physical chemical and analytical to the physical chemical characterization of NCEs.
- Calculate physical chemical and analytical parameters.
- Participate to the Quality Control of the non-clinical formulations in order to allow the achievement of non-clinical studies while assuring the quality required at the level of the realized studies and the respect of the schedules and priorities.
- Take part in the writing of study reports.
- Follow the working and security procedures
Specific professional/technical expertise and key skills required:
- Master/Bachelor/graduate A1: ANALYTICAL CHEMISTRY
- Min years' Experience in a regulated (GLP/GMP) pharmaceutical environment: 2-3 years
- International experience a plus
- Mandatory skills: team player, exp. in a similar position/environment, compliant/rigorous (understands the importance of following procedures in detail)
- English: able to read/write SCIENTIFIC DOCUMENTS
- French: mandatory: fluent
Scope of work:
- The physical chemical evaluation of NCEis.
- The characterization of NON-CLINICAL FORMULATIONS of NCE's.
- The development and validation of chromatographic methods for the development and the GLP QUALITY CONTROL of non-clinical formulations of NCEs.
- Apply physical chemical and analytical to the physical chemical characterization of NCEs.
- Calculate physical chemical and analytical parameters.
- Participate to the Quality Control of the non-clinical formulations in order to allow the achievement of non-clinical studies while assuring the quality required at the level of the realized studies and the respect of the schedules and priorities.
- Take part in the writing of study reports.
- Follow the working and security procedures
Specific professional/technical expertise and key skills required:
- Master/Bachelor/graduate A1: ANALYTICAL CHEMISTRY
- Min years' Experience in a regulated (GLP/GMP) pharmaceutical environment: 2-3 years
- International experience a plus
- Mandatory skills: team player, exp. in a similar position/environment, compliant/rigorous (understands the importance of following procedures in detail)
- English: able to read/write SCIENTIFIC DOCUMENTS
- French: mandatory: fluent
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik