Job Title: Document Control Specialist. As a Document Control Specialist, you will be responsible for prepping, scanning, inspecting, compiling, and assembling projects with accuracy in a timely manner. Your tasks will include taking a 'stack' of documents, removing all obstructions like paper clips...
Helps identify document control process improvements to streamline processes in document control or to adjust to changes in quality and regulatory requirements. Administers and maintains Midmark Corporations’ regulated document control processes, manual and electronic, in accordance with FDA and ISO...
The Document Control Specialist provides support to the operations and sales departments with every aspect of document control. The Doc Control Specialist will download test equipment. The Doc Control Specialist will create computer generated labels for job sites. The Doc Control Specialist supports...
Ensures and maintains customer satisfaction according to company standards of quality and output by prepping, scanning, inspecting, compiling, assembling and binding documents. ...
The Document Specialist prepares, edits, files, and assembles various types of documentation such as reports, technical documents, records, or correspondence. The Documentation Specialist is responsible for file maintenance and record-keeping, as well as locating and removing file material upon requ...
The ideal candidate will have 3+ years of word processing experience, including creating, formatting and revising documents; converting PDFs; and using document comparison software. Maintain flexibility in scheduling to cover shifts in the absence of other Document Specialists as needed. Ability to ...
Document Specialist (1st, 2nd, 3rd ). MJ Morgan Group is seeking a motivated Document Specialist to join our team. Sorting, Scanning, Searching and assembly the documents. ...
Responsible for preparing and scanning paper documents according to customer specifications and directions. Responsible for logging document/box numbers assigned during scanning for future retrieval. Assist other team members with document preparation and indexing. Ability to trouble-shoot computer ...
Performs routine department rounding to ensure compliance with all infection prevention and control policies and procedures as applicable and shares observations with appropriate leadership teams* Participates in facility Environment of Care Rounds and documents findings appropriately* Responsible f...
Primary responsibility of the GMP Quality Assurance Senior Specialist is to work as a team member to uphold compliance and maintenance of the Company’s cGMP (Current Good Manufacturing Practices) and Quality systems to in-house and/or external specifications, standards, and regulations. Cambri...
Location: 127 Public Square - Cleveland, Ohio 44114 JOB BRIEF The primary responsibility of a Documentation Specialist in the Derivatives Group is to negotiate ISDA documentation between Key and our counterparty clients. Prepare, review and negotiate ISDAs, Amendments, Pledge Agreements, Guarantees ...
The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above. The Specialist I, Supplier Quality will. Preferred at least 1 year of experience in quality and/or manufacturing in a pharmaceutical, biotech, or biologics cGMP regulated manufacturing environment preferre...
Clinical Documentation provides a formalized approach to promote accurate and complete medical record documentation reflecting a patient's true severity of illness and risk of mortality. The CDS reviews inpatient medical records and identifies opport Clinical, Specialist, Clinic, Healthcare, Medical...
We have an exciting opportunity for an Administrative Assistant!. This role will provide administrative support to division staff. At least three years' experience in a responsible administrative position; bookkeeping, accounting experience or training a plus. ...
Hims & Hers is seeking an experienced Quality Control Operations Specialist to join our Quality Unit. The Quality Control Operations Specialist role is responsible for the inspecting and/or testing of product(s) before, during and after manufacturing process(es) to ensure products align with company...
DME Documentation & Prior Auth Specialist. Medical Documentation Specialist. Proactively securing the necessary documentation for ongoing coverage to prevent any delays in services or billing. Retrieve and collect necessary medical documentation from healthcare providers, ensuring completeness and a...
Job Title: Associate, Document Specialist. Day to day work is separating and opening mail, prepping documents for scanning and some glass copies and other duties as assigned. ...
The Quality Control Specialist is responsible for ensuring that products meet established standards of quality, reliability, usability, and performance. Now hiring a Quality Control Specialist for a production company in Independence. Identify opportunities to improve quality control processes and r...
Eagle Integrated Services is searching for a Quality Assurance Specialist with Food Supply Chain experience in the Dayton, Ohio area!. Perform Food Vulnerability Assessments (FVAs) and Mission Assurance Assessments at sites worldwide. ...
Completes concurrent and/or retrospective documentation reviews of the medical record to determine the clinical validation of the documented diagnoses and/or procedures. Supports Documentation Improvement Task Force efforts to educate and reinforce the use of CDI Guides/Evidence Based Diagnostic Cri...
To apply for this Administrative Assistant position, please submit your resume to independence@areatemps. Qualified candidates must have previous administrative experience, must be computer literate, must have strong customer service skills, and must have a professional demeanor. ...
The Hoxworth Blood Center (HBC) is recruiting for a Quality Assurance/Regulatory Compliance (QARC) Specialist 2 position, to provide support to the QARC Department of HBC. QARC Specialist 2, Hoxworth Blood Center, Department of Quality Assurance. Quality Assurance, QA, Compliance, Pharmaceutical, Te...
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Support QA Operations team to investigate product quality complaints, quality events, incidents and CAPAs associated with materials or supplier services. The site also houses GMP manufacturing suites, and quality labs available to clients. Suppler Quality Management (SQM) and Audit Programs for the ...
Authorization to work lawfully in the US without sponsorship from Wood is required.Exceptional office, computer (Microsoft Word and Excel) and math skills.High school diploma or GED required, a college degree is a plus.Self-motivated and capable of working with minimal supervision.Able to handle mul...