Validation Specialist
Virtual Vocations Inc
Working remotely in a part-time capacity, the Pharmacy Validation Specialist will verify medical insurance eligibility, document data accurately, and meet daily production quotas while ensuring member records are precise. Key responsibilities Verifies medical insurance eligibility data Accurately documents data gathered and meets daily production quotas Utilizes multiple computer systems to work efficiently and provides excellent customer service Required qualifications High School diploma, GED, or equivalent combination of experience Experience with health insurance is preferred but not required Proficiency in Word and Excel Experience in the healthcare field is helpful but not required Strong attention to detail and organizational skills
- Job Description: 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 help ensure the required...Suggested
$128.47k - $208.77k
...Caterpillar Autonomous Program and plays a critical role in delivering high‑quality, technology‑ready autonomous platforms. The Autonomy Validation Lead will drive System Integration and Validation (SI&V) activities, primarily conducted in laboratory environments and closely...SuggestedFull timePart timeWork at officeRemote workRelocationRelocation packageFlexible hours- Summary : 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 for GMP equipment and utilities. Support...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
- ...worldwide. For more details, please visit : Job TitleEXPANSION Validation SpecialistJob DescriptionBusiness: Pharma SolutionsDepartment:... ...to the Validation Supervisor, the Validation Specialist executes validation and qualification protocols of manufacturing...SuggestedContract workWork at officeWorldwide
- Responsibilities: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, and validation testing activities.Required Skills...
- ...your potential? Join Team Novo Nordisk and help us make what matters.The PositionPlan, manage & perform low to moderately complex validation projects and activities. Support engineers with writing change requests and conducting/writing deviation investigations. Support...Work at officeLocal area
- ...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
- ...plans et les cahiers des charges et vous définissez les solutions de mise en œuvre. Vous coordonnez les dessinateurs, gérez les métrés et les validations clients, participez aux réunions de chantier et assurez la transition vers les équipes d’exécution. #J-18808-Ljbffr...
- ...Responsible for supporting all aspects of the Computer Systems Validation (CSV) Lifecycle for the Validation Department to ensure all... ...Technology, or a related discipline. 3–5 years of experience as a CSV Specialist or in a comparable role within the pharmaceutical or...Work at office
$59.52 - $82.73 per hour
job summary: Join Our Client as a Validation Specialist in Portsmouth, NH an industry leader driving biotech innovation! Seeking a CSV Specialist Level 3 in Vacaville with expertise in Computer System Validation, 21 CFR Part 11, and GAMP guidelines. Lead projects and...Hourly payContract workTemporary workWork experience placement- ...will oversee project execution, develop scope statements, estimates and staffing plans, and interface with clients while leading validation professionals. Requirements include 10+ years in validation/quality service and project management, knowledge of ISPE/PDA guidelines...
$110.71k - $145.3k
...of multiple myeloma. Legend Biotech is seeking a Sr. CSV/CQV Specialist as part of the Manufacturing & Supply team based in Raritan, NJ... ...be responsible for providing Commissioning, Qualification and Validation support to all computerized systems in the cGMP Clinical and Commercial...Permanent employmentFull timeTemporary workFor contractorsWork experience placementWork at officeLocal areaWorldwideFlexible hours- ...Validation Specialist The Validation Specialist is responsible for ensuring that our solutions meet the highest standards of quality, accuracy, and compliance. The scope of this job includes validating and verifying that implementations align with client requirements...Full timeWork experience placementWork at office
- ...Job Details Job Title: Validation Specialist Location: Meriden, CT Work Arrangement: Hybrid About the Role At BrandNu, a Caldic Company, our strength lies in inspiring solutions to address our customer's challenges in the pharmaceutical market. Our...
$96k - $120k
...Lyell Immunopharma, Inc. is seeking a Quality Assurance Specialist to oversee compliance in a cell therapy manufacturing environment. The role involves providing QA oversight for Facility, Equipment, Utility, and Computer System programs, ensuring adherence to GMP requirements...- ..., Canada, and South America. Professional Summary Experienced professional in laboratory protocol review, document revision, and validation of laboratory computerized systems (CSV) and SOPs. Skilled in LIMS and Empower, with extensive experience in laboratory instrument...
- What we are looking for: The Validation Specialist II coordinates and implements various activities for compliant and effective support of the Secant Group Validation functions conforming to ISO 13485, internal, and customer requirements. Responsible for performing multiple...
$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- ...Assurance team is expanding, and we're looking for a process validation professional with hands-on experience and a strong command of... ...validation life cycle.The Principal Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance...Full timeH1bVisa sponsorshipWork visa
$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- ...realize your potential? Join Team Novo Nordisk and help us make what matters.The PositionPrimary responsibility is to provide/lead validation services required for the successful delivery of IT & Automation projects.RelationshipsReports to Senior Project Manager, Site...Work experience placementLocal areaShift work
- Computer Systems Validation (CSV) SpecialistLocation: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families.The Computer Systems Validation (CSV) Specialist helps to lead team members to assess new and changing computer systems to...Full timeRelocation package
- 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 validation documentation...
- ..., 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
- ...dynamic healthcare environment dedicated to accuracy, compliance, and quality patient care.DutiesReview NLP-generated HCC coding output.Validate assigned codes against available documentation.Identify unsupported, inaccurate, or missing codes.Make corrections in the platform...Flexible hours
- ...Optimal in Warren, MI seeks a Labor Time Technician to time, validate, and optimize vehicle disassembly and reassembly processes. You will analyze time data and validate service procedures directly on vehicles, driving efficiency and accuracy across maintenance tasks....
- ...Supporting Product Lifecycle Management (PLM) implementation, the remote Computer Systems Validation Specialist will develop validation documentation, assist with system configuration, execute user acceptance testing, and ensure compliant system adoption in a regulated...Contract workRemote work
- ...Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Computer System Validation Specialist. Responsibilities: Performs and leads computer system validation projects related to authoring and executing...
$105.28k - $150.4k
Role Description The Computer System Validation (CSV) Lead is responsible for developing, executing, and maintaining the validation strategy for GxP-regulated computerized systems supporting manufacturing, laboratory, and quality operations. This role ensures that all...Full time
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