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Job opening ID99 Posting titleTraining Specialist Roles and responsibilitiesAssist with the development and delivery of training and instruction designed to increase the knowledge and understanding of the Penumbra Quality System, GMP and production processes. ?Provide training4/26/2016 Alameda, CA Save This Job
Location:Audubon, PA Job Code:RAPMKB0515 Description The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products.6/22/2016 Audubon, PA Save This Job
Madison, WIFull-time Company Description We develop and manufacture fully functioning human cells in industrial quantities to precise specifications. Our proprietary iCell Operating System (iCell O/S) includes true human cells in multiple cell types (iCell products), human5/25/2016 Madison, WI Save This Job
Location:Audubon, PA Job Code:ADSWH0615 Description The primary function will be to manage and organize all Quality Documentation that is required by Globus Medical, Inc. and other regulatory agencies. This will include issuing, maintaining, controlling, and auditing5/23/2016 Audubon, PA Save This Job
Job Location Tucson, Arizona Essential Duties Operates and maintains laboratory equipment. Assembles reagents, kit orders, and other products for shipment to customers in accordance with standard protocols. Performs service assay work for customers in accordance with standard4/25/2016 Tucson, AZ Save This Job
Location: Boulder, Colorado Job Description: Provide technical writing support for Batch Production Records, Solution Production Records, Standard Operating Procedures. Provide technical writing and investigation support for manufacturing deviation reports. Support review of5/24/2016 Boulder, CO Save This Job
Department: Quality Assurance Job Title: Quality Systems Specialist Reports To: Manager, Quality Systems Description: Quality Systems Specialist performs a wide variety of duties including, but not limited to, Quality Management Systems (QMS) performance oversight, data5/17/2016 Philadelphia, PA Save This Job
Application Deadline: May 31, 2016 Location: Schaumburg, Illinois, USA Job Summary / Overview: To provide Quality Assurance support and guidance for customer complaints received by managing the Sagent customer complaint program. Proactively support the existing quality systems5/15/2016 Schaumburg, IL Save This Job
Job Description: This position will have responsibility for supporting product disposition activities and provide Quality oversight of the cGMP biologics manufacturing activities conducted at Alder BioPharmaceuticals? Contract Manufacturing Organizations (CMO). This role5/25/2016 Bothell, WA Save This Job
Location:Audubon, PA Job Code:IRPMLB0216 Description The International Regulatory Affairs Specialist writes, submits and gains approval of product registrations and other submissions to international Regulatory agencies. This position entails development of submissions in6/22/2016 Audubon, PA Save This Job
This position will support global clinical supply operations and logistics to meet strategic business objectives. Expected to have knowledge regarding clinical supply planning, including analysis and reporting of supply/demand trends, production performance, and issue5/25/2016 Bothell, WA Save This Job
Location: Michigan Marrone Manufacturing, Bangor, MI Reports to: Production Supervisor or Manager Summary Marrone Michigan Manufacturing LLC (M3) is a wholly-owned subsidiary of Marrone Bio Innovations, Inc. (NASDAQ: MBII), a leading global provider of biopesticides for5/22/2016 Bangor, MI Save This Job