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Part-time Quality Assurance Consultant - Beerse, Belgium
Eingestellt von Elevate Direct
Gesuchte Skills: Consultant
Projektbeschreibung
Part time Quality Assurance Consultant - Beerse, Belgium
Primary Tasks and responsibilities
Investigate deviations related to departmental activities. The investigations, including corrective and preventive actions and impact assessments of the products, needs to be documented in the J&J deviations handling system. Assist in Change controls and suppliers management
Follow up customer returns and destruction. Products/services are investigated physically and impact assessment on quality and compliance is performed, before the products/services can be taken back for further use.
Deliver GMP GDP training to departmental personnel in order to assure operational personnel has an appropriate understanding of the Good Practices. Assist in the routine activities of the department with doc and training administration
Assist in check rounds and internal audits in the activities of the department. The goal of these self-inspections is to perform an in-depth review of the operation in view of the applicable cGMP regulations.
Review and approve quality related procedures. These procedures assure the day-to-day activities are performed in accordance with the GXP regulations. Procedures are controlled by the J&J document control system.
Work in close collaboration with Quality Representatives and Quality Representatives of J&J Organizations
Assist in the preparations of external and internal inspections related to overall quality and compliance.
Work in line with the Safety, Health and Environmental principles.
Deliver GMP training to departmental personnel in order to assure operational personnel has an appropriate understanding of the Good Manufacturing Practices.
Assist in check rounds and internal audits in the activities of the department. The goal of these self-inspections is to perform an in-depth review of the operation in view of the applicable cGMP regulations.
Review and approve quality related procedures. These procedures assure the day-to-day activities are performed in accordance with the cGMP regulations. Procedures are controlled by the J&J document control system.
Review and approve master data related to departmental activities.
Review and approve the master batch records, based on the approved request for the departmental activities. These batch records ensure the activities will be performed consistently according to the cGMP regulations.
Perform batch record review immediately after finalization of the departmental activities. This process assures the activities are performed in accordance to the cGMP regulations.
Additional information about the process
Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.
This job with Johnson & Johnson is a temporary assignment and is being managed by Kelly Services on behalf of Johnson & Johnson. Successful candidates will be placed at the Johnson & Johnson assignment and managed by Kelly Services
If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.
Primary Tasks and responsibilities
Investigate deviations related to departmental activities. The investigations, including corrective and preventive actions and impact assessments of the products, needs to be documented in the J&J deviations handling system. Assist in Change controls and suppliers management
Follow up customer returns and destruction. Products/services are investigated physically and impact assessment on quality and compliance is performed, before the products/services can be taken back for further use.
Deliver GMP GDP training to departmental personnel in order to assure operational personnel has an appropriate understanding of the Good Practices. Assist in the routine activities of the department with doc and training administration
Assist in check rounds and internal audits in the activities of the department. The goal of these self-inspections is to perform an in-depth review of the operation in view of the applicable cGMP regulations.
Review and approve quality related procedures. These procedures assure the day-to-day activities are performed in accordance with the GXP regulations. Procedures are controlled by the J&J document control system.
Work in close collaboration with Quality Representatives and Quality Representatives of J&J Organizations
Assist in the preparations of external and internal inspections related to overall quality and compliance.
Work in line with the Safety, Health and Environmental principles.
Deliver GMP training to departmental personnel in order to assure operational personnel has an appropriate understanding of the Good Manufacturing Practices.
Assist in check rounds and internal audits in the activities of the department. The goal of these self-inspections is to perform an in-depth review of the operation in view of the applicable cGMP regulations.
Review and approve quality related procedures. These procedures assure the day-to-day activities are performed in accordance with the cGMP regulations. Procedures are controlled by the J&J document control system.
Review and approve master data related to departmental activities.
Review and approve the master batch records, based on the approved request for the departmental activities. These batch records ensure the activities will be performed consistently according to the cGMP regulations.
Perform batch record review immediately after finalization of the departmental activities. This process assures the activities are performed in accordance to the cGMP regulations.
Additional information about the process
Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.
This job with Johnson & Johnson is a temporary assignment and is being managed by Kelly Services on behalf of Johnson & Johnson. Successful candidates will be placed at the Johnson & Johnson assignment and managed by Kelly Services
If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Organisation/Management