Clinical Documentation Specialists are responsible and accountable for the day-to-day management and success of the Continuous Documentation Improvement Project to include all modalities, acting as a liaison with specific department staff, speaking, meeting and educating physicians, residents and mi...
As a Clinical Documentation Improvement Specialist, you will be responsible for improving the overall quality and completeness of clinical documentation by expediting clarification to clinical documentation. Clinical Documentation Improvement Specialist. We are seeking an experienced and detail-orie...
Supports the quality review process for quality of care complaints and reviews, with guidance from senior team members by: preparing materials and reports for grievance meetings, cases, reviews, referrals, or other mechanisms as requested; preparing documentation, records, and information as directe...
The technical writer will create and update the technical documentation associated with the following:. ...
The Lead Technical Writer is responsible for creating, updating and maintaining Cilium documentation as a whole, the main part of it being developer and user documentation. You will be at the forefront of our users' experience for both Cilium OSS and Cilium Enterprise, making the most technically ad...
Required Licenses/Certifications: Registered Cardiovascular Invasive Specialist. ...
The Technical Writer is responsible for writing, editing, formatting, and managing the publication and translation of customer-facing documents for in vitro diagnostic Xpert tests and GeneXpert instrument systems. This position is part of the Technical Publications Team within Regulatory Affairs New...
Writes about technical subjects for technical and nontechnical audiences; assists in reformatting content for various media types, (landing site, monitors, etc. Adecco is hiring immediately for a Technical Writer role with a local client in Santa Clara, CA. Consult with engineering and technical sta...
Quality Assurance in a pharmaceutical, medical device or drug manufacturing company. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. Authors or approves procedures, work instructions and othe...
The Quality Assurance Specialist I plays a critical role in ensuring the quality and compliance of products and processes within the organization. This role is responsible for monitoring and evaluating quality assurance standards, conducting audits, identifying areas for improvement, and implementin...
Quality Assurance (QA) Analyst II. Quality Assurance certifications, preferably. A minimum of three (3) years of advanced Quality Assurance experience. Creating and effectively executing test planning, manual test case authoring, scripting of automated tests, test execution, defect management, testi...
We’re looking for a seasoned, principal technical writer with a proven track record of writing content that simplifies the user experience. This is a principal writer role, focused on our new cloud-delivered management platform, Strata Cloud Manager. ...
Co-ordinates and prepares document packages for regulatory submissions from all areas of the organization.Collects all materials required in submissions, license renewal, and annual registrations.Keeps abreast of regulatory procedures and changes.May interact with regulatory agencies.Works on proble...
Regional Compliance Specialist. Assist in turning around low-performing divisions' compliance numbers and contribute to the continuous improvement of the company’s compliance program and processes. In collaboration with Region Safety Directors, GMs, and division safety, develop and implement strateg...
Collaborate with executive and administrative assistants on cross-functional tasks. ...
The Senior Quality Assurance (QA) Specialist - Supplier Quality will play a pivotal role in ensuring that all external suppliers and third-party vendors adhere to Vaxcyte’s quality standards and regulatory requirements. Supplier Quality Agreements: maintain quality agreements with key suppliers to d...
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You will primarily be responsible for: development, execution, evaluation and ongoing supervision of individual and project action plans in order to improve patient care outcomes; create policies and procedures; conduct independent assessment of patients and their current treatment plans; collaborat...
Quality Compliance Specialist will perform work under general supervision. Compliance, Audit, Regulatory, NCR, ISO, Data entry, Quality assurance, Regulatory compliance, Gmp. Position Overview In compliance with FDA, European MDD/MDR & ISO regulations, the Sr. General scope of this position is to as...
Take full ownership of end-to-end Enya Labs technical documentation. Write and update technical documentation. Maintain and update all technical research and documents and edit and improve developer written and business prose. Partner and collaborate with Product, Engineering and Marketing teams to ...
We are currently searching for a skilled professional to join a well-known client’s team as a Clinical Application Specialist remotely. The Clinical Application Specialist role will contribute to data analysis plan documentation and deliver data analysis results to epidemiologists. Advanced Clinical...
As the Document Control Specialist, you will be responsible for developing and maintaining document transmittals, records, and systems for our client's first commercial scale projects. Perform project document control activities such as ECN (Engineering Change Notice), managing the distribution matr...
Clinical Practice Quality Specialist - Hematology / Oncology / Stem Cell Transplant. Clinical Practice Quality Specialists are Registered Nurses with advanced degrees who utilize evidence-informed practice to facilitate and lead improvements in patient care and in the work environment. The Clinical ...
Licensed Psychologist (PsyD)- Focused Therapy Specialist. ...
Looking for someone to provide technical writing support to a process development technical team - drafting documents, editing, and working with scientists to enter figures. ...