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Prolacta Bioscience Inc. ? City of Industry, CA Posted 27 days ago Apply Now Email Job Save Job Job Snapshot Full-Time Experience - At least 5 year(s) Degree - 4 Year Degree Biotechnology Training Job Description Company Prolacta is the pioneer in human milk-based6/28/2016 City of Industry, CA Save This Job
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 training5/31/2016 Alameda, CA Save This Job
This position will have responsibility for supporting the Drug Substance & Drug Product Validation effort; including process characterization, preparations for BLA filing, process validation and GMP support activities in collaboration with Contract Manufacturing Organizations7/27/2016 Bothell, WA 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.6/26/2016 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:Manassas, VA Job Code:1491 # of openings:1 Description Job Qualifications: Track received parts against EBOMs and MBOMs. Receive parts into program inventory and enter them into SAP. Inventory so that parts and materials can be located and assembled into build kits.7/18/2016 Manassas, VA 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 standard5/30/2016 Tucson, AZ 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 auditing6/26/2016 Audubon, PA 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, data6/20/2016 Philadelphia, PA 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 of5/29/2016 Boulder, CO Save This Job
Location: Boulder, Colorado Job Description: Own / manage the KBI Boulder IT Validation Master plan for all computer systems. Align site validation plans with Corporate IT validation requirements. Manage the execution and documentation of the site IT Validation Program assuring6/28/2016 Boulder, CO Save This Job
Location: Boulder, Colorado Job Description: Performs compliance review on the following records: batch record (includes on-the-floor review of records); release data. Reviews and approves Master Batch Records and Solution Records. Works directly with manufacturing, the6/28/2016 Boulder, CO 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 in6/26/2016 Audubon, PA Save This Job
ID 2016-1954 Job Location US-FL-Clearwater Category Customer Service/Support Position Status Regular Full-Time Position Schedule Monday-Friday Shift 8am-5pm Alternative Schedule .. More information about this job: Overview: Responsible for building, managing, and7/27/2016 Clearwater, FL Save This Job
SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of ena7/22/2016 Hawthorne, CA Save This Job