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Overview Join our team as a PRN Nuclear Medicine Technologist in Montclair, NJ.    Fulfilling your purpose begins here:  People First, Always. Here’s how we take care of our people:  Competitive salaries, support teams and growth opportunities. Your team is bigger than your department:  Hackensa...

Overview Join our team as a day shift, full-time, Nuclear Medicine Tech in Montclair, NJ.   Fulfilling your purpose begins here:  People First, Always. Here’s how we take care of our people:  Medical, vision, dental health insurance, health savings account / flexible spending, competitive pay, p...

Manage document preparation of CMC regulatory submission documents to Client standards and ensure final document compliance to ensure submission content meets formatting requirements.Manage the logistical process in the authoring system for CMC regulatory submissions.This process includes coordin...

LHH Recruitment Solutions is seeking a qualified Japanese Document Review Attorney to join our dynamic team. Translate documents from Japanese to English and from English to Japanese. Review and analyze legal documents for relevance, privilege, and confidentiality. Ensure accurate and timely iden...

LHH Recruitment Solutions is seeking a qualified Japanese Document Review Attorney to join our dynamic team. Translate documents from Japanese to English and from English to Japanese. Review and analyze legal documents for relevance, privilege, and confidentiality. Ensure accurate and timely iden...

Temporary Document Review Specialist deals with meeting projects with tight deadlines and the demands of being available to work in any of our locations and shifts. Providing support in the Printing/copying and scanning of client's documents by being flexible to work weekends, holidays, and overt...

GRM Document Management, a leading provider of life-cycle records and information management solutions, is seeking a senior accountant to join our team. Assisted in budget development, auditing procedures, compiling documentation, and coordinating. ...

DescriptionThe document AI and automation function of Chubb works across the global line of business to drive operational efficiency in the full lifecycle of insurance. ...

Innova Solutions is immediately hiring for a Nonclinical Regulatory Document and Scientific Writer. Regulatory Document and Scientific Writer,. Partner with Drug Metabolism and Pharmacokinetic (DMPK) and Bioanalytical (BA) Subject Matter Experts (SMEs) to author, review and track regulatory docum...

The company continues to demonstrate technological leadership by bringing proprietary innovation and new levels of cost efficiency to document storage, digital/electronic document management, data protection and certified destruction clients. These services include: Document Storage Services, Ele...

Kyocera Document Solutions America, Inc is a group company of Kyocera Document Solutions Inc. When you join Kyocera Document Solutions America, Inc. In addition, were a Great Place to Work and we really mean it! Kyocera Document Solutions America, Inc. Your role will involve defining the digital ...

Serving a diverse base of industries such as healthcare, government, legal, finance and human resources, GRM delivers its clients services such as digital conversion, advanced data capture solutions, document management systems, workflow automation, legacy data archiving, compliance and governanc...

Do you excel at document control and have experience supporting large scale, complex construction projects and/or engineering teams? If so, consider joining our team! Parsons is seeking a local** Senior Document Control Specialist **to support our portfolio of projects. Scan hard copy h...

Assist in Documentation Audit programs for GMP documents. Distribute approved documentation to appropriate personnel, track receipt of documentation, reconciliation and maintain distribution matrices. Assist in the administration of the company GMP Records Retention Policy, including document ima...

Quality Document Administrator. Routing documents in SAP system for reviews / approvals (training will be provided). Filing and organizing paper documents. ...

The company continues to demonstrate technological leadership by bringing proprietary innovation and new levels of cost efficiency to document storage, digital/electronic document management, data protection and certified destruction clients. These services include: Document Storage Services, Ele...

The Clinical Document Specialist is responsible for ensuring accurate and compliant physician documentation in the electronic medical record. The Clinical Documentation Specialist (CDS) responsibilities include assisting in clarifying documentation regarding the patient’s diagnoses and/or procedu...

Create project plans and Lead diverse teams in the development/review and update of all required documentation (for electronic and published materials) and project planning including but not limited to manuals, processes, procedures and protocols. Develop roll-out strategies for change management...

Temporary Document Review Specialist deals with meeting projects with tight deadlines and the demands of being available to work in any of our locations and shifts. Providing support in the Printing/copying and scanning of client’s documents by being flexible to work weekends, holidays, and overt...

The Document Controls Manager is responsible for the development, maintainance and management all Renewables & Energy Solutions (RES) documentation and documentation systems. The Document Control Manager plays a critical role in the management of documented information, ensuring that documented ....

Armand Corporation, an award-winning M/WBE Construction Management firm celebrating over 33 years in the industry, is seeking a full-time  Document Control Specialist  in all disciplines for a federal construction project related to complex rail, transit, and other transportation projects ...

Reviews, recommends edits and standardization of procedures, work instructions, specifications, forms, and any other related documentation to assure alterations to the original records are properly performed, documented, substantiated, reviewed and approved by the document owners. Maintains docum...

Job responsibilities * Articulate product vision and contribute to development and execution of the product roadmap * Maintain effective relationships with sponsors, and key partners to manage stakeholder expectations from requirement definition through delivery * Au...

Nonclinical Regulatory Document and Scientific Writer,. Experience reviewing regulatory documents, DMPK and BA reports, and non-GLP/GLP data and notebooks. Training on in-house document repository system will be provided. Experience with CTD documents and nonclinical study reports for submission ...