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Manufacturing Documentation Specialist Jobs

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QA DOCUMENTATION SPECIALIST

Cytokinetics

Department: Regulatory & Compliance Job Location: South San Francisco Cytokinetics is a late-stage biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators as potential treatments for debilitating diseases in which muscle

11/21/2016  South San Francisco, CA  Save This Job

Quality Assurance Specialist (4043)

Aegerion Pharmaceuticals, Inc.

Req Id 4043 - Posted 09/29/2016 - United States - Massachusetts - Cambridge - Quality ? Job Description Print Preview Apply Apply using LinkedIn? Save Job Email Job to Friend Return to List The Quality Assurance (QA) Specialist is responsible for oversight of selected

11/2/2016  Cambridge, MA  Save This Job

Quality Assurance Specialist

Corium International

Tracking Code 2177 Job Description The Quality Assurance Specialist is responsible for supporting Quality Assurance operations, compliance, systems, and regulatory affairs functions. Essential Duties: An employee in this position must be able to perform the essential job

10/17/2016  Grand Rapids, MI  Save This Job

Specialist, Quality

Sagent Pharmaceuticals

Application Deadline: October 31, 2016 Location: Schaumburg, Illinois, USA Job Summary / Overview: Responsible for the execution of batch record reviews and associated product quality issue resolution. Authorizes shipments from Sagent?s contract manufacturing organizations

10/25/2016  Schaumburg, IL  Save This Job

Production Specialist (#194)

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

11/5/2016  Madison, WI  Save This Job

Regulatory Affairs Specialist (U.S.)

Globus Medical

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.

11/2/2016  Audubon, PA  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

10/8/2016  Tucson, AZ  Save This Job

Sr. Quality Assurance Specialist 4

Ardelyx

Quality Assurance Fremont, California Apply Description Sr. Specialist, Quality Assurance Ardelyx is building an integrated biopharmaceutical company with a gastrointestinal and cardio-renal focus. Our mission is to serve patients through the discovery, development and

11/1/2016  Fremont, CA  Save This Job

Sr. Quality Assurance Specialist 4

Ardelyx

Quality Assurance Fremont, California Apply Description Sr. Specialist, Quality Assurance Ardelyx is building an integrated biopharmaceutical company with a gastrointestinal and cardio-renal focus. Our mission is to serve patients through the discovery, development and

11/1/2016  Fremont, CA  Save This Job

Senior Quality Compliance Specialist

Argos Therapeutics

Senior Quality Compliance Specialist About Us Senior Quality Compliance Specialist Description The Senior Quality and Compliance Specialist drives and executes the development, implementation, execution and improvement of systems and procedures required to ensure regulatory

10/18/2016  Durham, NC  Save This Job

Quality Compliance Specialist

Argos Therapeutics

Quality Compliance Specialist About Us Quality Compliance Specialist Description The Quality and Compliance Specialist 1). Executes all aspects of the Quality Agreement program, including maintenance of internal tracking databases of Quality Agreement implementation and

10/18/2016  Durham, NC  Save This Job

Regulatory Affairs Specialist

InTouch Health

Location: Santa Barbara, CAType: Full TimeMin. Experience: Experienced InTouch Health is the leading telehealth solution company enabling specialist physician care anytime, anywhere. We are looking for an experienced, self-starting Regulatory Affairs Specialist to join our team!

10/18/2016  Santa Barbara, CA  Save This Job

Sr. Quality Assurance Specialist

Concert Pharmaceuticals

Job Summary: The position will provide support for the Quality Assurance group. The candidate will work with cross functional teams to maintain internal quality systems for GxP activities. Responsibilities: ? Write, review and approve Standard Operating Procedures (SOP) and Forms

10/23/2016  Lexington, MA  Save This Job

Specialist-Technical Writer #202/225

KBI Biopharma

Location: Colorado Job Description: Provide technical writing and investigation support for manufacturing deviation reports. Support review of batch documentation to enable batch release milestones to be met. Provide technical and operational support in the writing and execution

11/6/2016  Boulder, CO  Save This Job

Specialist-Technical Operations #221

KBI Biopharma

Location: Colorado Job Description: Provide technical writing and investigation support for manufacturing deviation reports. Support review of batch documentation to enable batch release milestones to be met. Provide technical and operational support in the writing and execution

11/6/2016  Boulder, CO  Save This Job

QA Specialist II #195

KBI Biopharma

Location: Colorado 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

11/6/2016  Boulder, CO  Save This Job

UP TO "Lead Regulatory Affairs Specialist"

Scientific Protein Laboratories

Company:Scientific Protein Laboratories Job Location(s):Waunakee, WI Start Date:ASAP Employment Term:Regular Employment Type:Full Time Hours per Week:40+ Work Hours (i.e. shift):days Starting Salary Range:Not Provided Required Education:Bachelor's Degree Required Experience:5

11/9/2016  Waunakee, WI  Save This Job

Traffic Specialist

CiDRA

Position Summary: The Traffic Specialist will have direct oversight to all freight/traffic related activities. This includes the coordination of all outgoing shipments, both domestic and international as well controlling inbound freight as needed. This position will ensure that

10/29/2016  Wallingford, CT  Save This Job

Process Validation Specialist

Argos Therapeutics

Process Validation Specialist About Us Process Validation Specialist Scope Support process validation for manual RNA and cellular manufacturing for autologous dendritic cell immunotherapies. Support comparability demonstration efforts for process improvements. Support

10/18/2016  Durham, NC  Save This Job

Patient Account Specialist

CCS Medical Holdings, Inc.

ID 2016-1982 Job Location US-TX-Farmers Branch Category Customer Service/Support Position Status Regular Full-Time Position Schedule Monday-Friday Shift 8am-5pm Alternative Schedule .. More information about this job: Overview: Position Summary: Ensures all new referrals

11/5/2016  Farmers Branch, TX  Save This Job