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Manufacturing Documentation Specialist Jobs

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Documentation Specialist

Quanterix

Lexington, MA Quanterix is an exciting early-stage company whose mission is to develop a game-changing platform that combines proprietary single-molecule sensitivity, multiplexing and full automation with its revolutionary Single Molecule Array (Simoa) technology. Located in

2/3/2016  Lexington, MA  Save This Job

Documentation Specialist

Acumentrics

Job Description: Develop, coordinate and maintain Engineering Change Orders (ECO) through the Documentation Control system. Ensure that document management systems are compliant with manufacturing practices and ISO standards. Responsibilities: Maintains Bills of Materials

12/27/2015  Westwood, MA  Save This Job

Process Specialist

SpaceX

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 enabling human life on

2/5/2016  Hawthorne, CA  Save This Job

Quality Assurance Specialist

Aprecia Pharmaceuticals

Job ID55 OverviewAs a small start company employees are needed who are willing to perform any activity in their department and help support all other departments when needed. This position shall work in documentation and support cGMP compliance. As a member of the Quality

12/22/2015  East Windsor, NJ  Save This Job

Formulation Specialist (#173)

Cellular Dynamics International

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), human

1/9/2016  Madison, WI  Save This Job

Manufacturing Science and Technology Specialist III/IV

Acceleron Pharma

About Acceleron: Acceleron is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel therapeutic candidates that regulate cellular growth and repair. The company is a leader in understanding the biology of the

12/13/2015  Cambridge, MA  Save This Job

Quality Assurance Compliance Specialist

Aprecia Pharmaceuticals

Job ID100 Overview Perform internal audits for Aprecia?s East Windsor, NJ facility and support the corporate vendor qualification program. Work with all departments on controlled documents and perform as designee for the Director when required. Also serves as the primary trainer

12/22/2015  Blue Ash, OH  Save This Job

Corporate Applications Specialist

High Throughput Genomics

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 standard

12/8/2015  Tucson, AZ  Save This Job

Assistant Document Specialist

Globus Medical

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 auditing

1/5/2016  Audubon, PA  Save This Job

Manufacturing Specialist #131

KBI Biopharma

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 of

2/9/2016  Boulder, CO  Save This Job

QA Specialist II #435

KBI Biopharma

Location: North Carolina Job Description: Performs compliance review on the following records: batch record/formulation record (includes on-the-floor review of records); release and stability data, method qualification/validation reports, stability protocols and development

1/10/2016  Durham, NC  Save This Job

Validation Specialist

Alder Biopharmaceuticals

This position will have responsibility for supporting the Validation effort; including process characterization, process validation and GMP support activities in collaboration with Contract Manufacturing Organizations (CMO). This role supports late stage clinical development and

2/8/2016  Bothell, WA  Save This Job

MSAT (Downstream)

Acceleron Pharma

Manufacturing Science and Technology Specialist (Downstream) About Acceleron: Acceleron is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel therapeutic candidates that regulate cellular growth and repair. The

12/13/2015  Cambridge, MA  Save This Job

NDT (Non-Destructive Testing) Supervisor - 2nd shift

SpaceX

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 enabling human life on

1/13/2016  Hawthorne, CA  Save This Job

Cycle Count Coordinator

K2M

Location: Corporate Office - Leesburg, VA Full Time Requisition Number: req187 Reports To: Inventory Management Specialist FLSA Status: Exempt Department: Operations Summary: The Cycle Count Coordinator works in a team oriented environment that partners closely with other

1/29/2016  Leesburg, VA  Save This Job

NDE LEVEL III R&D Supervisor

SpaceX

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 enabling human life on

1/21/2016  Hawthorne, CA  Save This Job