Search Results: 14,546 vacancies
...Description
Job Title:
Manager , Risk Adjustment, Clinical Quality Documentation
FLSA Status:
Job Code :
Pay Grade:
Core Bay... ...skills
Management
* This position supervises staff : Specialists, RNs, Coders, NPs
Qualifications
Education
*...
Suggested
Shift work
As a QA Document Specialist II, you will play a pivotal role at Penumbra providing timely and accurate support of quality processes related to Document Services to ensure compliance with Penumbra procedures and regulatory requirements. Follow standards and procedures in...
Suggested
Hourly pay
Holiday work
Temporary work
Local area
Shift work
...working hours, patterns, and locations to suit you and the business.
What You'll Be Doing
Job Scope: Generally responsible for document management for projects and personnel. This work will be performed under general supervision.
Primary responsibilities will...
Suggested
Hourly pay
Holiday work
Flexible hours
...Job Title: Technical Writer/Document Specialist
Location: Remote
Duration: 12 Months
Job Responsibilities:
Contribute to an innovative initiative focused on the development and production of cutting-edge autonomous delivery robots.
Collaborate...
Suggested
Remote job
Shift work
...Opportunity
Description
We're looking for a Quality Assurance Specialist , working in Pharmaceuticals and Medical Products industry... ...Job description:
Reviews computer system validation documentation, preferably with GCP systems
Supports IT validation...
Suggested
...purpose to business. We are currently recruiting for a Senior Quality Specialist.
Job Description
The Senior Quality Specialist... ...related to quality assessment; performance improvement; clinical documentation review; risk management; infection prevention and control;...
Suggested
Relocation
...and join us on our journey towards global connectivity!
Quality Specialist, Machining
As our first Quality Specialist, you will be tasked... ...communicate with engineers to improve our part designs and documentation.
Role
Inspect all mechanical parts built in the...
Suggested
Permanent employment
Worldwide
...Job Description
Job Description AGS has an IMMEDIATE opening for a Document Controls Specialist.
Responsibilites :
Maintain databases and existing filing systems (alphabetical, numerical, chronological, etc.)
Word processing of business documents
Setup...
Suggested
Hourly pay
Holiday work
Full time
Immediate start
Flexible hours
...2023
Description
The Bay Area Air Quality Management District (Air District) is a... ...applications for the position of Air Quality Specialist I/II in the Compliance & Enforcement... ...for laboratory analysis; prepares documentation of findings; consults with citizens on...
Suggested
Holiday work
Full time
Temporary work
Work experience placement
Remote job
Flexible hours
...We are seeking a highly motivated individual to join as Specialist/ Senior Specialist, Quality Systems at our South San Francisco location. The successful candidate will provide assistance for the Document Control program, including day-to-day document processing, document...
Suggested
Temporary work
Local area
Flexible hours
...future of radiology and clinical operations through software, automation and AI.
We are looking for a Quality Specialist to support & coordinate SOP training, document control and configuration management, as well as internal quality audits to comply with ISO-13485 and...
Suggested
Local area
Remote job
Flexible hours
...Description
Job Description Overview:
The Remote Temporary Document Specialist performs document control by creating, reviewing, or editing... ...under pressure within established timeframe and provide quality work product;
~ Interact effectively and professionally...
Suggested
Remote job
Temporary work
...Stability Specialist I or II, QC Description: Seeking a Stability Specialist Temporary to join the Quality Control group. The QC Stability Specialist Temporary will be responsible for QC stability program; organization stability studies, management o Specialist, Quality...
Suggested
Temporary work
...execution of action plans to improve customer experience.
Understand and ensure all relevant MDLZ locations comply with the customer's quality expectations.
Serve as the Quality lead to investigate customer issues and ensure the identification of root causes and close...
Suggested
Relocation package
...reading!
Position Summary:
We are seeking a (Senior) Quality Documentation Manager to oversee the electronic Quality Management System... ...accuracy, quality, and integrity. The Quality Documentation Specialist is responsible for the creation, implementation, and revision...
Suggested
Full time
Temporary work
Local area
Flexible hours
...improving peoples lives with our health care products.
The Quality Assurance Specialist, GMP provides Quality support for Petaluma site and... ...laboratories.
**Key Activities:**
Review and approve GMP documents (e.g., production batch records, clinical labelling...
Holiday work
Contract work
Temporary work
Flexible hours
...Familiarity and proficiency in performing all responsibilities of the Quality Associate.
Subject Matter Expertise in one or more specific... ...Files per approved procedures. Reviews records for good DHF documentation practices and adherence to DHF Document Change Control...
Local area
$80k - $110k
...Job Summary:
Coordinates quality, accreditation, regulatory and licensing (AR&L), patient safety and risk management activities for the medical center. Provides clinical, educational, consulting, and coordinating support to assigned areas. Uses nurses licensure...
Full time
Local area
Shift work
The Senior Associate, Training and Document Management is responsible for Document Control and Training Coordination activities in the Quality Systems team at GeneFab while complying with company and regulatory requirements. This function supports GMP training and documentation...
Hourly pay
Contract work
...Sr. Quality Engineer – Supplier Quality (Onsite)
The Quality Engineer will provide expertise and support compliance of Supplier Controls with applicable Regulations and Standards (ISO 13485:2016, IVDR, FDA 21 CFR 820, etc.). They will lead Supplier Quality Team Meetings...
