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Quality Validation Engineer
Eingestellt von Harvey Nash IT Recruitment Belgium
Gesuchte Skills: Engineer, Engineering, Support
Projektbeschreibung
Quality Validation Engineer
Period 22/01/2018 to 21/04/2018
Work Location: Lessines
Description:
PRODUCT DEVELOPMENT - PROJECT SUPERVISOR VALIDATION
Tasks:
Project management:
* Organization and coordination of project activities related to Manufacturing:
- Development activities
- Support/expertise for the development of the product documentation
- Validation activities (engineering tests, qualifications, process validation and cleaning)
- Bid activities (production of stability batches for submissions)
- Implementation-related activities (training, follow-up of FOC)
* Creation and follow-up of the implementation plan to ensure that the objectives of the project are achieved in a timely manner
* Participation in project meetings as a representative of the Manufacturing
* Project budget monitoring
Project documentation:
* Creation and follow-up of the project documentation in collaboration with the various departments (CCR, URS, FS, DS, Risk Analysis ...)
* Monitoring protocols and reports
* Follow-up of the creation of the procedures, PCS, BOM, etc ...
YOUR PROFILE
* Validation Engineer with a minimum of 3 years of experience
* Experience in the pharmaceutical field
* Knowledge in project management and GMP
* English fluent in writing and speaking (French is a plus)
* Easy communication
* Organization skills
* Knowledge of production and validation processes
Period 22/01/2018 to 21/04/2018
Work Location: Lessines
Description:
PRODUCT DEVELOPMENT - PROJECT SUPERVISOR VALIDATION
Tasks:
Project management:
* Organization and coordination of project activities related to Manufacturing:
- Development activities
- Support/expertise for the development of the product documentation
- Validation activities (engineering tests, qualifications, process validation and cleaning)
- Bid activities (production of stability batches for submissions)
- Implementation-related activities (training, follow-up of FOC)
* Creation and follow-up of the implementation plan to ensure that the objectives of the project are achieved in a timely manner
* Participation in project meetings as a representative of the Manufacturing
* Project budget monitoring
Project documentation:
* Creation and follow-up of the project documentation in collaboration with the various departments (CCR, URS, FS, DS, Risk Analysis ...)
* Monitoring protocols and reports
* Follow-up of the creation of the procedures, PCS, BOM, etc ...
YOUR PROFILE
* Validation Engineer with a minimum of 3 years of experience
* Experience in the pharmaceutical field
* Knowledge in project management and GMP
* English fluent in writing and speaking (French is a plus)
* Easy communication
* Organization skills
* Knowledge of production and validation processes
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges