Validation Specialist
Virtual Vocations Inc
Detail-oriented and mission-driven, the full-time Validation Specialist will support healthcare quality improvement initiatives by reviewing medical records, investigating discrepancies, and documenting findings in a remote environment. Key responsibilities Investigate and adjudicate discrepancies between hospital and CDAC abstractions to determine the gold standard response Document explanations for discrepancies and provide educational feedback to hospitals or CDAC Perform medical record abstraction as needed to support module production goals Required qualifications Minimum of two years of experience in a hospital, healthcare, or medical record review environment At least one year of abstraction experience with above-average data accuracy and productivity Thorough knowledge of medical terminology Proficiency with Microsoft Office applications High school diploma or equivalent, with additional technical training in medical record review preferred
- ...AI/ML Model Validation Specialist Location: Des Plaines; HYBRID (3 days onsite) Overview This role leads independent validation and governance of models across the enterprise — spanning AI systems, machine learning, and traditional statistical models — ensuring...Suggested
- Job-ID32495586Reference26-01079Remote50% RemoteResponsibilities:Lead validation activities for Labware LIMS 8 implementationAuthor and review IQ/OQ/PQ, RTM, and validation documentationEnsure compliance with GXP, CSV, and regulatory standardsSupport audits, inspections...Suggested
- Job-ID33111878Reference26-01830Summary :This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area.This role will be supporting validation leads to...Suggested
- ...instrumentation. • Coordinate all services provided by vendors, ensuring vendors meet all site requirements. Schedule/plan/execute validation activities and preventive maintenance of laboratory equipment. Skills:• Demonstrated scientific technical writing ability. •...SuggestedWork at officeImmediate startShift work
- Job-ID33134493Reference26-01862 Job Summary: We are seeking a hands-on Equipment Qualification & Process Validation Contractor to support the Enterprise Quality - Change Management & Systems organization. The contractor will be responsible for executing qualification activities...SuggestedFor contractors
- Job-ID32848489Reference26-01442 Requirements: Support cleaning validation activities, protocol execution, sampling, and documentation. Perform temperature mapping and requalification of controlled temperature units. Execute IQ/OQ/PQ, requalification, and periodic review...
- ...consultant will use his/her knowledge of FDA cGMP and related regulations and guidelines, and specific knowledge of computer system validation (CSV) methodologies and principles to perform CSV on a variety of laboratory systems in the QC department at the Canton site .The...Work at officeImmediate start
- Job-ID32981060Reference26-01708Job summary:We are seeking an experienced Validation Specialist to support validation activities in a GMP-regulated environment.Roles and Responsibilities:10 years of experience in Validation within Pharma, Biotech, or Life SciencesHands-on...
- ...real impact on people’s health around the world. Together, we’re improving health and improving lives.Labcorp is seeking a Validation Specialist, Immunoassay to join ourteam in Indianapolis, IN!Work Schedule: Monday-Friday 8am-5pmJob Responsibilities:Performs procedures...Temporary workCasual workInternshipMonday to FridayFlexible hours
- ...Job summary: We are seeking an experienced Validation Specialist to support validation activities in a GMP-regulated environment. The ideal candidate will have strong hands-on expertise in equipment, facility, utility, and/or process validation, including IQ, OQ,...
$93.5k
...Job Duties JOB TITLE & Employer Name: Validation Specialist for Harvard Bioscience, Inc. LOCATION: 119-14th Street NW., Suite 100, St. Paul, Minnesota 55112. JOB DUTIES: Develop and implement validation documentation that include Standard Operating Procedures...Full timeRemote workShift work- ...The Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP computerized systems. Primary responsibilities include: qualification of laboratory instruments, setup of computers and instruments, troubleshooting...Work experience placement
- ...Job Title Lead validation activities for Labware LIMS 8 implementation Author and review IQ/OQ/PQ, RTM, and validation documentation Ensure compliance with GXP, CSV, and regulatory standards Support audits, inspections, and validation testing activities...
- ...Functional Requirements (FRS), Configuration/Design Specifications, Risk Assessments, Requirement Traceability Matrices (RTMs), Validation Plans (VMP), Test Plans, and Validation Summary Reports (VSR). Execute validation lifecycle documents including Installation Qualification...Contract work
- ...Job Title Key Responsibilities Perform commissioning, qualification, validation, and maintenance activities within the facility. Oversee multiple CQV projects, providing updates and coordinating with internal teams and external vendors. Lead and support...Work at office
$60k - $75k
...Validation Specialist Who we are? As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients' lives accessible to as many people as possible. As a world leader in sterile single dose, we have 10 sites...Hourly payFor contractorsInternshipWork at officeShift work- ...Position Overview We are seeking a detail-oriented and experienced Validation Specialist to join our growing team. In this role, you will be instrumental in ensuring that our computerized systems and software meet rigorous regulatory compliance, data integrity,...Temporary work
- ...Validation Specialist (Life Sciences) Develop and maintain SOPs, user manuals, validation protocols, and regulatory submission documents. Translate complex scientific and technical concepts into clear, concise documentation. Collaborate with SMEs to gather and...
- ...Validation Specialist 1539 Fillmore St, Twin Falls, ID 83301, USA Full-time Job Description Norco is currently seeking an individual to fill our Validation Specialist position. The Validation Specialist ensures accurate and timely submission of new claims and claims delayed...Full timeLocal areaFlexible hours
$41.73k - $51.5k
...Overview TISTA is seeking a detail-oriented Validation Specialist to support healthcare quality improvement initiatives. In this role, you will review medical records, investigate and adjudicate discrepancies between hospital and CDAC abstractions, determine the gold...Temporary workWork at officeRemote workFlexible hours- ...JOB TITLE: Validaton Specialist Lead JOB LOCATION: Milford, Ma Must be onsite WAGE RANGE*: 45 - 50/ hour JOB NUMBER:... ...run and execute CV Protocols. Proven work experience as a Validation Engineer or similar role. Strong knowledge of validation...Hourly payTemporary workWork experience placementLocal areaFlexible hours
$107.1k - $160.7k
..., engineers, interior designers, consultants, sustainability specialists, and technologists are passionate about the power of design.... ...that support and enhance our communities. The Commissioning and Validation role provides crucial services to confirm equipment and...Full timeTemporary workPart timeCasual workWork at officeLocal areaImmediate startFlexible hours- Job-ID32818102Reference26-01398 Job Description: We are seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. The ideal candidate will be responsible for planning, executing, reviewing, and approving...
- ..., engineers, interior designers, consultants, sustainability specialists, and technologists are passionate about the power of design.... ...and throughout the building lifecycle. As a Commissioning / Validation Specialist, you will support the delivery of high-quality commissioning...Full timeTemporary workPart timeFor contractorsCasual workWork at officeLocal areaFlexible hours
- Computer Systems Validation Specialist IIILocation: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.The Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems to...Full timeRelocation package
- Job-ID32940527Reference26-01625 Requirements: Experience supporting validation activities, including equipment, process, facility, computerized systems, and documentation review. Preferred experience in high-speed aseptic filling operations and sterile manufacturing environments...
- ...the responsibilities listed below, this position is also responsible for performing initial testing and setup procedures (e.g., validation, verification, calibration, sensitivity studies) for new or replaced instruments; supporting assay development; and contributing...Local area
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who... ...for the following position: ~ Supplier Component Validation Specialist Description: Responsible for component testing, sampling...Full time
- ...Job Description Job Description Validation Specialist Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device IT & Human Resources disciplines in New Jersey. The Validation Specialist performs validation...Work at officeFlexible hours
- Job Description Job Description Leads, coordinates and performs all functions of quality reviews (routine, pre-bill, policy driven and incentive plan driven) for inpatient coding across multiple HSCs Assists in ensuring HSC coding staff adherence with coding...
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