1st Shift, Monday- Thursday, 4:00 PM - 2:30 AMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records. Understands a
1st Shift, Monday- Thursday, 4:00 PM - 2:30 AMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records. Understands a
1st Shift, Monday- Thursday, 4:00 PM - 2:30 AMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records. Understands a
1st Shift, Monday- Thursday, 4:00 PM - 2:30 AMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records. Understands a
Onsite full time in Billerica, MA. The Quality Document Coordinator is an individual contributor who is responsible for conducting day to day processing of controlled documents for cGMP operations. Responsible for compliance in accordance with Document Management procedures and will assist with ongoing Quality documentation deliverables driven by business objectives and identified by management. Must have experience with eForms (creation, processing) and h
Onsite full time in Billerica, MA. The Quality Document Coordinator is an individual contributor who is responsible for conducting day to day processing of controlled documents for cGMP operations. Responsible for compliance in accordance with Document Management procedures and will assist with ongoing Quality documentation deliverables driven by business objectives and identified by management. Must have experience with eForms (creation, processing) and h
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