Rensselaer, NY (Onsite) We are seeking a QA Validation Specialist to support facilities compliance ... The ideal candidate will review technical documentation, validate data, and ensure compliance with ...
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Rensselaer, NY (Onsite) We are seeking a QA Validation Specialist to support facilities compliance ... The ideal candidate will review technical documentation, validate data, and ensure compliance with ...
Quick apply
Rensselaer, NY (Onsite) We are seeking a QA Validation Specialist to support facilities compliance ... The ideal candidate will review technical documentation, validate data, and ensure compliance with ...
Rochester, NY · On-site
Determines and documents validation conclusions based on data, observations, and investigation outcomes. Collaborates cross-functionally with Operations, Engineering, Quality Assurance, Quality ...
Rochester, NY · On-site
Determines and documents validation conclusions based on data, observations, and investigation outcomes. Collaborates cross-functionally with Operations, Engineering, Quality Assurance, Quality ...
Rensselaer, NY · On-site
Rensselaer, NY (Onsite) Job Summary: The QA Validation Specialist will support facilities ... Generate and review technical documentation for QA compliance * Analyze vendor data, verify ...
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Rensselaer, NY · On-site
Rensselaer, NY (Onsite) Job Summary: The QA Validation Specialist will support facilities ... Generate and review technical documentation for QA compliance * Analyze vendor data, verify ...
Determines and documents validation conclusions based on data, observations, and investigation outcomes. Collaborates cross-functionally with Operations, Engineering, Quality Assurance, Quality ...
Determines and documents validation conclusions based on data, observations, and investigation outcomes. Collaborates cross-functionally with Operations, Engineering, Quality Assurance, Quality ...
Rochester, NY · On-site
Validation Specialist Who we are? As a French pharmaceutical industrial group, we strive to make ... Documentation & Reporting • Authors validation protocols, reports, and supporting documentation ...
Rochester, NY · On-site
Validation Specialist Who we are? As a French pharmaceutical industrial group, we strive to make ... Documentation & Reporting • Authors validation protocols, reports, and supporting documentation ...
Validation Specialist Position Summary * Typical working hours are Monday-Friday 8 AM-5 PM * This ... Responsibilities include developing the appropriate and required protocol documents in accordance ...
Validation Specialist Position Summary * Typical working hours are Monday-Friday 8 AM-5 PM * This ... Responsibilities include developing the appropriate and required protocol documents in accordance ...
Winchester, KY · On-site
Validation Specialist Position Summary * Typical working hours are Monday-Friday 8 AM-5 PM * This ... Responsibilities include developing the appropriate and required protocol documents in accordance ...
Winchester, KY · On-site
Validation Specialist Position Summary * Typical working hours are Monday-Friday 8 AM-5 PM * This ... Responsibilities include developing the appropriate and required protocol documents in accordance ...
Indianapolis, IN · On-site
... documentation, CMMS systems, and electronic validation platforms such as KNEAT, Veeva, or Val ... Validation Specialist- Indianapolis, IN Core Responsibilities • Develop, author, and execute ...
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Indianapolis, IN · On-site
... documentation, CMMS systems, and electronic validation platforms such as KNEAT, Veeva, or Val ... Validation Specialist- Indianapolis, IN Core Responsibilities • Develop, author, and execute ...
Mechanicsburg, PA · On-site
$55K - $90K/yr
Validation Specialist (US-O) The Validation Specialist role has a national salary range of $55,000 ... Create documents within the eQMS and assign them to appropriate personnel * Database entry
Mechanicsburg, PA · On-site
$55K - $90K/yr
Validation Specialist (US-O) The Validation Specialist role has a national salary range of $55,000 ... Create documents within the eQMS and assign them to appropriate personnel * Database entry
Marion, NC · On-site
Validation Specialist Marion, NC, USA 12 months W2 contract Must have experience supporting medical device manufacturing under ISO 13485 Writing test protocols within KNEAT Gx Knowledge of CQV ...
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Marion, NC · On-site
Validation Specialist Marion, NC, USA 12 months W2 contract Must have experience supporting medical device manufacturing under ISO 13485 Writing test protocols within KNEAT Gx Knowledge of CQV ...
Instrument Validation Specialist Location: Andover, MA (Onsite) Job Summary: Seeking an Instrument ... Work with systems like LIMS, QTS, Empower, and document repositories * Apply FDA and regulatory ...
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Instrument Validation Specialist Location: Andover, MA (Onsite) Job Summary: Seeking an Instrument ... Work with systems like LIMS, QTS, Empower, and document repositories * Apply FDA and regulatory ...
Rensselaer, NY · On-site
Rensselaer, NY (Onsite) Job Summary: The QA Validation Specialist will support facilities ... Generate and review technical documentation for QA compliance * Analyze vendor data, verify ...
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Rensselaer, NY · On-site
Rensselaer, NY (Onsite) Job Summary: The QA Validation Specialist will support facilities ... Generate and review technical documentation for QA compliance * Analyze vendor data, verify ...
Validation Specialist Lynkx Staffing LLC specializes in placing talented professionals in the ... Assembling validation related documents; and filing/archiving approved documents * Maintaining ...
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Validation Specialist Lynkx Staffing LLC specializes in placing talented professionals in the ... Assembling validation related documents; and filing/archiving approved documents * Maintaining ...
Job Summary The Operations Validation Specialist at BioLegend will perform and administer ... Contribute to the generation and review of required documentation that support the validation ...
Job Summary The Operations Validation Specialist at BioLegend will perform and administer ... Contribute to the generation and review of required documentation that support the validation ...
Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the ... Support regulatory inspections and audits by preparing documentation, responding to inquiries, and ...
Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the ... Support regulatory inspections and audits by preparing documentation, responding to inquiries, and ...
The Milestone & Validation Specialist will be responsible for assisting the Milestone and ... Coordinate documentation control for the project and file appropriately for Closeout procedures.
The Milestone & Validation Specialist will be responsible for assisting the Milestone and ... Coordinate documentation control for the project and file appropriately for Closeout procedures.
The Milestone & Validation Specialist will be responsible for assisting the Milestone and ... Coordinate documentation control for the project and file appropriately for Closeout procedures.
The Milestone & Validation Specialist will be responsible for assisting the Milestone and ... Coordinate documentation control for the project and file appropriately for Closeout procedures.
Albuquerque, NM · On-site
Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the ... Support regulatory inspections and audits by preparing documentation, responding to inquiries, and ...
Albuquerque, NM · On-site
Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the ... Support regulatory inspections and audits by preparing documentation, responding to inquiries, and ...
Wilmington, MA · On-site
$90K - $120K/yr
Validation Specialist & Project Manager ???? Drive Validation & Expansion in Nuclear Medicine On ... validation documentation • Maintain inspection-ready validation records Expansion Project ...
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Wilmington, MA · On-site
$90K - $120K/yr
Validation Specialist & Project Manager ???? Drive Validation & Expansion in Nuclear Medicine On ... validation documentation • Maintain inspection-ready validation records Expansion Project ...
Juncos, PR · On-site +1
Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are ... Document execution activities in accordance with protocol instructions and data integrity ...
Juncos, PR · On-site +1
Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are ... Document execution activities in accordance with protocol instructions and data integrity ...
$15.87 - $21.28
3% of jobs
$21.28 - $26.70
3% of jobs
$26.70 - $32.12
3% of jobs
$32.12 - $37.54
8% of jobs
$39.98 is the 25th percentile. Wages below this are outliers.
$37.54 - $42.96
16% of jobs
$42.96 - $48.38
9% of jobs
The median wage is $50.58 / hr.
$48.38 - $53.80
17% of jobs
$58.95 is the 75th percentile. Wages above this are outliers.
$53.80 - $59.22
16% of jobs
$59.22 - $64.64
8% of jobs
$64.64 - $70.06
7% of jobs
$70.06 - $75.48
8% of jobs
$15
$50
$75
| Aspect | Document Validation Specialist | Data Entry Clerk |
|---|---|---|
| Required Credentials | High school diploma, certifications in document verification or quality control | High school diploma or equivalent, basic computer skills |
| Work Environment | Offices, data centers, or remote settings focused on document review | Offices, data entry centers, or remote work handling data input |
| Employer & Industry Usage | Financial, healthcare, legal sectors | Various industries including retail, healthcare, finance |
| Search & Comparison Intent | Understanding roles involving document accuracy and validation | Looking for data input or clerical roles |
The Document Validation Specialist focuses on verifying the accuracy and authenticity of documents, often requiring certifications and attention to detail. In contrast, a Data Entry Clerk primarily inputs data into systems with less emphasis on document verification. Both roles are essential in data management but serve different functions within organizations.

Hello,
I hope you're doing well.
My name is Mahalakshmi, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a QA Validation Specialist based in Rensselaer, NY (Onsite), with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at mahalakshmi.n@intellectt.com OR +1 (732) 737 8381
Job Title: QA Validation Specialist
Location: Rensselaer, NY (Onsite)
We are seeking a QA Validation Specialist to support facilities compliance and quality assurance activities in a highly regulated environment. The ideal candidate will review technical documentation, validate data, and ensure compliance with GMP/GDP standards while collaborating with QA and Facilities teams.
Required Skills:
Preferred Skills:
Thanks & Regards,
Mahalakshmi
Junior Recruiter
Intellectt Inc
mahalakshmi.n@intellectt.com
Direct: +1 (732) 737 8381
Sourced by ZipRecruiter
51 - 200 Employees
Iselin, NJ, US
2018