Jobs: associate ii qa document control

Piper Companies is currently seeking a QA Document Control Associate for an opportunity in Summit, New Jersey (NJ), to join a global biopharmaceutical company delivering life-saving medicines to patients with serious diseases. Responsibilities of the QA Document Control Associate Manage electronic document system, including document change control and...

POSITION SUMMARY:Under the direction of the QA Document Control Supervisor, the QA Systems Associate – Document Control, will be responsible for searching, reviewing, comparing and verifying data using Excel spreadsheet, MasterControl, and SAP OpenText. This individual will work closely with IT Validation team for the purpose of data review and...

POSITION SUMMARY:Under the direction of the QA Document Control Supervisor, the QA Systems Associate – Document Control, will be responsible for searching, reviewing, comparing and verifying data using Excel spreadsheet, MasterControl, and SAP OpenText. This individual will work closely with IT Validation team for the purpose of data review and...

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.Our client, a leading pharmaceutical company is hiring a QA Associate Specialist – Document Control on a contract basis. Please only local candidates to Summit NJ.Work Location: Summit NJPay: $30-31/hour W2Required Skills: • Document Control & Reporting...

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.Our client, a leading pharmaceutical company is hiring a QA Associate Specialist – Document Control on a contract basis. Please only local candidates to Summit NJ.Work Location: Summit NJPay: $30-31/hour W2Required Skills: • Document Control & Reporting...

DescriptionThe Document Control Coordinator II supports Operations, R&D, RA, and QA activities by preparing, reviewing, routing, approving, archiving and implementation of Quality System documents.ResponsibilitiesPerform Document Control preparation, review, routing, approval, and archiving of Quality System documents according to established...

Job DescriptionJob DescriptionLeading Long Island manufacturer of nutraceuticals and nutritional supplements seeks a hands-on entry to senior level Document Control Associate in Quality Assurance - Technical Affairs & Document Control.The QA Technical Affairs/Document Control Associate is responsible for supporting the Technical Affairs/Document group in...

Description The Document Control Coordinator II supports Operations, R&D, RA, and QA activities by preparing, reviewing, routing, approving, archiving and implementation of Quality System documents. Responsibilities Perform Document Control preparation, review, routing, approval, and archiving of Quality System documents according to established...

Since 2001, RealStreet has connected management executives for the construction industry to contractors working on commercial and government projects. As a leading firm in the country which specializes entirely in senior level construction employment, we have cultivated long-term relationships with many of the industry's leading companies enabling us access...

Since 2001, RealStreet has connected management executives for the construction industry to contractors working on commercial and government projects. As a leading firm in the country which specializes entirely in senior level construction employment, we have cultivated long-term relationships with many of the industry's leading companies enabling us access...

Natural Organics, Inc. a leading Manufacturer and Distributor of Dietary Supplements is seeking a Document Control Associate . This position will provide administrative document control support, assist with coordination, re-certification and submission of all certified programs (i.e. cGMP, Organic, Safety, etc.); knowledge of FDA regulations and DSHEA...

Job DescriptionJob DescriptionNatural Organics, Inc. a leading Manufacturer and Distributor of Dietary Supplements is seeking a Document Control Associate. This position will provide administrative document control support, assist with coordination, re-certification and submission of all certified programs (i.e. cGMP, Organic, Safety, etc.); knowledge of FDA...

Job DetailsLevel ExperiencedJob Location ADMA Biologics - Boca Raton, FLPosition Type Full TimeEducation Level 4 Year DegreeTravel Percentage NoneJob Category PharmaceuticalDescription ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to...

Job DescriptionJob DescriptionDocument Control SpecialistABOUT THE ORGANIZATION Rohadfox Corporation is a professional services firm offering Construction Management, Program Management, and Engineering Design services. Founded in 1976, Rohadfox’s quality of work, integrity, and commitment has built decades-long relationships, maintaining a solid...

Job DetailsLevel ExperiencedJob Location ADMA Biologics - Boca Raton, FLPosition Type Full TimeEducation Level 4 Year DegreeTravel Percentage NoneJob Category PharmaceuticalDescription ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to...

Pay Rate : $34-$38/hr Job Description: - 2+ years of Document Control & Reporting Experience, - Veeva experience preferred - Technical troubleshooting - Self motivated, independent, great communication - Experience working cross-functionally Position Summary: The Quality Assurance Document Control ( QADC ) Associate Specialist supports the ...

Leading Long Island manufacturer of nutraceuticals and nutritional supplements seeks a hands-on entry to senior level Document Control Associate in Quality Assurance - Technical Affairs & Document Control.The QA Technical Affairs/Document Control Associate is responsible for supporting the Technical Affairs/Document group in the creation, review,...

Job DescriptionJob DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QA Specialist II to work for a leading Greater Los Angeles area biopharmaceutical company.Pay Rate: $35-45/hour depending on experience.Responsibilities:Support clinical product...

Customer Job Quality Document Control Specialist Job ID: 24-02189 Onsite with Hybrid option after training The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various *** departments the documentation that is necessary to perform cGxP activities....

Job Title: Quality Assurance Document Control (QADC) Associate SpecialistLocation: Bothell, WA*OnsiteTop Skills:- 1 to 3 years of Document Control experience in a regulated environment- 1 to 3 years of EDMS Experience(Veeva or similar Electronic Doc Management System)- 1 to 3 years with MS Office 365(Specifically Word styles and formatting) **PLEASE DO NOT...