Clinical Documentation Specialist - Rochester, NY

This role will review product calibration traceability papers to make them fully compliant with ISO standards. · Review current product calibration traceability papers. · Making edits to make the papers fully compliant (versus the benchmark paper and the ISO 17511 standards). · ...

This role supports validation activities for new products within a medical device manufacturing facility. · Review current product calibration traceability papers. · Determine adequacy to the requirements outlined in ISO 17511. · ...

CACI is looking for a full-time Document Control Specialist to join our expanding team in Rochester. · In this position you will support the design and manufacture of ruggedized military radio products and systems. · ...

The Clinical Documentation Specialist facilitates accurate documentation for severity of illness, expected risk of mortality, complexity of care and quality in the medical record.This involves extensive record review and interaction with physicians, health information management ...

CACI is looking for a full-time Document Control Specialist to join our expanding team in Rochester NY. · Creation and management of part numbers in ERP and PLM systems as required · ...

The CDS facilitates accurate documentation for severity of illness, expected risk of mortality, complexity of care and quality in the medical record. · This involves extensive record review and interaction with physicians, health information management professionals, and nursing ...

+The CDS facilitates accurate documentation for severity of illness, expected risk of mortality, complexity of care and quality in the medical record. · This involves extensive record review and interaction with physicians, health information management professionals, and nursing ...

This is a contract position in the Operations Product Support team at Client, located in Rochester. · This role supports validation activities for new products within a medical device manufacturing facility. · ...

+Job summary · The CDS facilitates accurate documentation for severity of illness, expected risk of mortality, complexity of care and quality in the medical record. · +ResponsibilitiesReviews medical record for completeness and accuracy for severity of illness (SOI), risk of mort ...

The Clinical Documentation Specialist will work under the direction of the CDI Director to facilitate standardization across the health-system and ensure alignment of high quality documentation. · Responsibilities include participating in recruitment and selection of CDI staff me ...

We are seeking a detail-oriented and highly organized Document Control Specialist to manage and maintain controlled documentation in compliance with FDA regulations, ISO standards, and internal quality systems. · Associate's or Bachelor's degree in a related field (Life Sciences, ...

Create and maintain work instructions SOPs troubleshooting guides and job aids Collaborate with subject matter experts engineers and operations teams to gather and validate technical content Research and analyze technical information to produce user-focused documentation Edit and ...

+Job Summary · Akodis is seeking a Document Control Specialist role in a Contract with a client located in Victor NY Ideally looking for applicants to have a solid background in FDA regulations ISO standards cGMP would come as a big plus.+ · ++Administer and maintain the Document ...

This is an overview of the job. · Act as change analyst for Document Change Orders (DCO's) and Deviations for all controlled documents within assigned departments. · ...

We are seeking a detail-oriented and highly organized Document Control Specialist to manage and maintain controlled documentation in compliance with FDA regulations, ISO standards, and internal quality systems. · Associate's or Bachelor's degree in a related field (Life Sciences, ...

We are seeking a detail-oriented and highly organized Document Control Specialist to manage and maintain controlled documentation in compliance with FDA regulations, ISO standards, and internal quality systems. · Administer and maintain the Document Control System (electronic and ...

We are seeking a detail-oriented and highly organized Document Control Specialist to manage and maintain controlled documentation in compliance with FDA regulations, ISO standards, and internal quality systems. · This role is critical to ensuring the integrity, accessibility, and ...

Gentis Solutions is seeking a Specialist Design (PCB Layout) to join their client's engineering team in Rochester NY This role focuses on printed circuit board PCB layout and design support across complex electrical and electronic systems. · Create and maintain PCB layouts in ali ...

+Job summary · Maintaining accurate documentation and ensuring compliance with safety protocols. · +ResponsibilitiesPerform diagnostic and interventional procedures such as angiography, biopsies, and embolizations. · Collaborate with multidisciplinary teams to provide exceptional ...

The Home Care Quality Assurance (QA) Specialist is responsible for monitoring evaluating and improving the quality of care delivered by the home health agency This role ensures compliance with CMS Conditions of Participation State regulations Star Ratings Value-Based Purchasing V ...