GMP BiotechPharma MFG AM
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POST DATE 8/27/2016
END DATE 10/18/2016
JOB DESCRIPTIONGMP Biotech/Pharma MFG (AM) AP5621446Smithfield, RI6 Month Contract*** NO THIRD PARTY SUBCONTRACTORS****** DO NOT SUBMIT ANY RESUMES THAT CANNOT WORK AS OUR W2 EMPLOYEE***Again, NO third party subcontractors!!! DO NOT submit any resumes that cannot work as our W2 employee!!Duties:Lead Manufacturing investigations and implement corrective and preventive actions.Lead and/or participate in the implementation of manufacturing activities in the areas of Safety, the Environment, Quality, Supply, and Cost Participate in process and equipment troubleshooting activities Independently author and execute new equipment commissioning and qualification protocols Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.Assess process performance by observation of floor operations and review of performance data with the objective of implementing process improvement solutions Assist with generation of training materials to improve shopfloor execution and coordinate training activities for the entire department (as needed) Assist with generation of validation protocols and execution of equipment and process validation Participate in regulatory inspectionsSkills:Must be able to work within and adapt to complex electronic systems such as SAP and Trackwise Must have the capacity to develop in-depth knowledge of manufacturing operations, including cell culture and purification operations, filtration, and culture media pre
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