Experience with an ERP environment for manufacturing and shop floor controls (BOMs, routings).

1 years’ experience in a GMP manufacturing environment.

Failure to achieve results can typically be overcome without serious effect on schedules and projects.

Typically works on focused individual assignments coordinates activities with others.

Can write routine reports and correspondence.

Has the ability to read and interpret documents such as rules, operating instructions and procedure manuals.

Frequently interacts with peers and supervisors builds internal and external relationships.

Coordinates information flow between self, team and/or departments.

Supervision is general with instructions given for routine work and detailed instructions given for new lines of work or special assignments.

Normally receives general instructions on routine work, detailed instructions on new assignments.

Works independently on routine assignments receives guidance for new assignments.

Works on assignments that are routine in nature where limited judgment is required.

Resolves task-related problems in straightforward situations.

Requires a moderate understanding of general job aspects and superficial understanding of the technical aspects of the job.

Acquires job skills and learns company policies and procedures to complete routine tasks.

Applies technical and procedural knowledge formal training or experience is required to perform the job effectively.

Completes moderately complex tasks following well-defined procedures may involve a variety of routine or established work processes.

Strong computer skills, including Microsoft Word and Excel.High aptitude and familiarity with laboratory instuments including pipettes, balances, and pH meters.Ability to accurately follow written procedures and annotated drawings.Supports the maintenance of visual production-management tools.Complies and insures compliance with all documentation and production record keeping.Monitors manufacturing compliance to procedures.Closely interacts with Engineering, Materials, and QA/QC departments in product change controls, deviations and technical troubleshooting issues.Ensures timely material availability, shop floor documentation completion and manufacturing work cell development.Supports the maintenance of QSR and GMP production in an FDA regulated environment.

Reviews and approves technical instructions and procedures to procure, assemble, and test molecular biology components and instrumentation.Filling, labeling and packaging of chemical reagents.Responsible for GMP production of Medical Diagnostic instrumentation associated with FDA approved components for implementation and integration into complex diagnostic assay systems.

Agena bioscience careers