Documentation Specialist: Average Salary in Santa Barbara, CA in 2024
Find out what the average Documentation Specialist salary is in Santa Barbara, CA
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Clinical Documentation Improvement Specialist
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...
QA Documentation Specialist
QA Documentation Specialist III. QA Documentation Specialist III. Maintains documentation manuals to ensure accuracy and current information. Supports the distribution and maintenance of GXP documentation. ...
Wastewater Lead Operator - Orange/Riverside/San Bernardino/San Diego
In 2012, Water Quality Specialists partnered with Coombs Service Group, California general contractor #1014254, to increase the scope and quality of maintenance services offered to our customers. In 2012, Water Quality Specialists partnered with Coombs Service Group, California general contractor #1...
Wastewater Lead Operator - Grade III or Higher Required
In 2012, Water Quality Specialists partnered with Coombs Service Group, California general contractor #1014254, to increase the scope and quality of maintenance services offered to our customers. In 2012, Water Quality Specialists partnered with Coombs Service Group, California general contractor #1...
Technical Writer (Environmental Science, Wildlife & Natural Resources)
The Technical Writer (Environmental Science, Wildlife & Natural Resources) specializes in producing professional biological and environmental reports. The Technical Writer will collaborate closely with a team of scientists, biologists, GIS analysts, data managers, technicians, and administrative sta...
Quality Specialist
Clinical Quality Specialist, GCP, Medical Device/Pharmaceuticals. Our client, a global medical device company, has engaged GForce Life Sciences to provide a Clinical Quality Specialist (GCP). This position will report to the Associate Director, Clinical Quality. Support inspection readiness activiti...
Technical Writer - Biotech
Collect, organize, summarize, write, and revise extensive, complex technical information in a concise manner for various audiences, assisting in the preparation of developed materials for reports, articles, manuals, specifications, presentation materials, illustrations and other technical and non- t...
Compliance Specialist
They are seeking a detail-oriented and experienced Compliance Specialist to join the compliance team. This role is critical in supporting the firm's compliance framework and maintaining a robust culture of compliance. Conduct regular compliance audits and risk assessments, identifying and mitigating...
Environmental Compliance Review Specialist (Reservist)
The Environmental Planning and Historic Preservation Cadre (EHP) announces the hiring of EHP Environmental Compliance Review Specialist (ECSP) position under FEMA's Reservist Program. Assist in the fulfillment of the Agency’s compliance with a range of federal environmental/historic regulations gove...
Air Quality Engineer/Scientist (Environmental Compliance Specialist)
Environmental Permitting and Compliance Specialist). Environmental Permitting and Compliance Specialist). Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our missio...
Senior Specialist Clinical Quality Assurance
The Senior Specialist, Clinical Quality ensures GCP compliance with SOPs, ICH and US FDA regulations, guidelines, and clinical study protocols. Senior Specialist, Clinical Quality Assurance - Hybrid (Los Angeles, California). This role maintains inspection readiness and interacts with Clinical Trial...
Administrative Assistant
Provide administrative and organizational support to the radiologists and clients. ...
Senior Quality Assurance Specialist
The Senior Specialist, Clinical Quality ensures GCP compliance with standard operating procedures, ICH and US FDA regulations and guidelines, and clinical study protocols. This position interacts cross-functionally with functional teams in Clinical Trials which include Clinical Operations, Regulator...
CMC Regulatory Technical Writer, Associate Director/Director
CMC Regulatory Technical Writer, Associate Director/Director. CMC technical document review and writing, authoring and compiling the CMC sections for global regulatory filings by working closely with the cross-functional teams including CMC, Quality, Clinical and Regulatory Affairs to ensure all CMC...
Quality Assurance Compliance Specialist
Supports Quality Assurance, and Quality Control activities to ensure operations are conducted in compliance with applicable regulations and standard operating procedures to ensure product quality is consistent with the specifications and facilitate batch disposition for commercial purposes. ...
Quality Assurance Compliance Specialist
Compliance Specialist I maintains Quality Compliance by being aware of quality requirements; preparing standards, metrics, standard operating procedure (SOP) management; supporting audits, Quality Investigations and Corrective and Preventive Actions (CAPA); analyzing and verifying documentation; and...
Administrative Assistant
Provides administrative supportto the unit. ...
Administrative Assistant - Remote/Online/Work From Home (PT/FT) - Hourly Rates Ranging From $15 up t
Administrative Assistant - Remote/Online/Work From Home (PT/FT) - Hourly Rates Ranging From $15 up to $26. The core duties and responsibilities of an Administrative Assistant revolve around supporting others. In order to perform their various duties, an Administrative Assistant must possess varied s...
Compliance Specialist
Join our expanding compliance team as a Compliance specialist! We are seeking a detail-oriented, proactive, and self-starting individual who is eager to grow and advance in the field of audits and corporate compliance. In this role, you'll play a crucial part in maintaining our company’s compliance ...
Documents/Records Specialist
Legal Support seeks a Production Specialist that has a keen eye for detail, communicates effectively, and is problem solver. Production Specialist Key Responsibilities:. Burn CD’s as well as copies and binds the produced documents to be mailed to the client. Quality check all documents before going ...
QUALITY ASSURANCE SPECIALIST GS/1910/11
Ensures that contractor is performing quality assurance (QA) of stored petroleum products, maintaining quality standards in compliance with MIL-STD 3400-C. The incumbent is the Quality Assurance Evaluator (QAE) for the alongside aircraft refueling contract. Incumbent is responsible for the quality o...
IT - Technical Writer - Mid
Job Title: Technical Writer - Mid. Technical Writer develops and maintains manuals, standards, procedures, and bulletins that enable Client to maintain compliance with all external and internal requirements and ensure public and employee safety. Take complex technical information and make it clear a...
Specialist- Quality Assurance
Position Purpose:The Specialist - Quality Assurance is responsible for ensuring that all calls adhere to the quality guidelines as set forth by the client and by Everise. ...
Technical Writer
Collaborate with subject matter experts to gather information and understand technical concepts. Create and maintain technical documentation including user manuals, installation guides, API documentation, release notes, and troubleshooting guides. Assist with other technical writing tasks and projec...
Evening Document Processing Specialist / Technicien(ne) en traitement de texte de soir
Evening Document Processing Specialist . As a Document Specialist, you will be providing firm-wide support using your advanced skills in Microsoft Office (Word, Excel, PowerPoint and Adobe). Technical tasks of document formatting/styling including conversion of PDF to Word, forensics utilizing compl...