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Associate Pilot Plant
Location:
US-RI-West Greenwich
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Our client in Rhode Island has an Associate Pilot Plant position.This position is with an industry leader working on site in Rhode Island. This is a temporary position with the possibility of extension.


Job Details:
Perform inventory management processes for pilot scale process development biopharmaceutical laboratory. General duties include, but not limited to material handling and coordination of raw materials, review of experiment bill of materials, and collaborating with supply chain partners to facilitate material requisitions. Other responsibilities include; performing goods receipt, transport & stocking of materials, pulling and kitting of materials, and routine inventory cycle counts. Must be able to lift up to 50lbs and push/pull heavy loads using material handling equipment. Performs routine preventative maintenance and standardization of benchtop analytical devices to such as automated cell counter, metabolic analyzers, and solution meters. Carries out laboratory tasks per plan and procedure in a team environment. Documents data and process information in accordance to good documentation practices. Performs laboratory safety evaluations. Performs daily cleaning and sanitization of the laboratory.

May support various experiment preparation and execution as directed to include, but not limited to; execution of cell culture, harvest and downstream purification process studies using 500 L scale pilot equipment including bioreactors, chromatography skids and filtration systems. Additional routine tasks may include equipment preparation such Clean-In-Place and Steam-In-Place, compounding media and buffer solutions, and sampling. Utilizes scientific principles in execution of experiments and analysis of experimental data. Documents data and process information in accordance to good documentation practice

Preferred Qualifications:

Prior hands-on experience with SAP and/or similar electronic inventory software. Pilot-scale or large-scale cell culture or downstream purification process development or manufacturing operation. Experience with automated and computer-controlled biopharmaceutical process equipment. Knowledge of process data compilation and analysis Demonstrated equipment troubleshooting skills. Excellent problem-solving capabilities and attention to detail. Experience collaborating within and across functional areas and outstanding customer focus Excellent written and verbal communication skills.

BioPharma Consulting JAD Group

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