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Data Integrity Associate 6305 Jobs in Raleigh, NC

Damco Solutions

Databricks Data Specialist

Raleigh, NC · On-site

... and integrity while working closely with data engineers. Responsibilities : • Conduct ... Associate Certification Company : Damco Solutions is a provider of IT solutions, services, and ...

MyEyeDr.

Sr. Administrator, People Systems

Raleigh, NC · On-site

$76K - $103K/yr

Lead continuous improvement initiatives by identifying opportunities to optimize HR technology, automate business processes, improve data integrity, and enhance the overall associate experience.

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All JobsData Integrity Associate 6305 JobsData Integrity Associate 6305 Jobs in Raleigh, NC

Data Integrity Associate 6305 information

See Raleigh, NC salary details

$14

$32

$54

How much do data integrity associate 6305 jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for data integrity associate 6305 in Raleigh, NC is $32.15, according to ZipRecruiter salary data. Most workers in this role earn between $23.85 and $38.08 per hour, depending on experience, location, and employer.

What is the difference between Data Integrity Associate 6305 vs Data Quality Analyst?

AspectData Integrity Associate 6305Data Quality Analyst
Primary FocusEnsuring data accuracy, consistency, and compliance within databasesAssessing and improving data quality through analysis and reporting
Required SkillsData validation, database management, attention to detailData analysis, quality metrics, reporting tools
Work EnvironmentHealthcare, finance, or corporate data teamsIT departments, data analytics teams
CertificationsTypically none required, but certifications like CDMP may helpData analysis certifications like CAP, CDMP beneficial

While both roles focus on data quality, the Data Integrity Associate 6305 primarily ensures data accuracy and compliance within databases, often in regulated industries. The Data Quality Analyst emphasizes analyzing and improving data quality through metrics and reporting. Both roles require attention to detail and familiarity with data management tools, but their day-to-day tasks and focus areas differ slightly.

What are popular job titles related to Data Integrity Associate 6305 jobs in Raleigh, NC?

For Data Integrity Associate 6305 jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Data Integrity Associate 6305 jobs in Raleigh, NC look for?

The top searched job categories for Data Integrity Associate 6305 jobs in Raleigh, NC are:

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Cities near Raleigh, NC with the most Data Integrity Associate 6305 job openings:

Data Integrity Associate 6305 jobs near you
Infographic showing various Data Integrity Associate 6305 job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 72% In-person, 14% Hybrid, and 14% Remote job distribution, with an average salary of $66,874 per year, or $32.2 per hour.

Quality Specialist - Batch Record Review

Equiliem

Raleigh, NC

$22 - $24/hr

Full-time

Posted 6 days ago

Job description

Quality Specialist II - Batch Record Review 
Raleigh, NC 
Pay: $22.00 - $24.00 per hour 
26-07733
Job Summary

The Quality Specialist II – Batch Record Review is responsible for reviewing manufacturing and packaging batch records to ensure compliance with current Good Manufacturing Practices (cGMP), internal quality standards, and regulatory requirements. This role supports product release activities by verifying production documentation, identifying discrepancies, and collaborating with Manufacturing and Quality teams to ensure accurate and compliant records. The position also supports quality systems, facility inspections, material status verification, and continuous improvement initiatives within a regulated manufacturing environment.

Job Responsibilities

  • Review manufacturing and packaging batch records for completeness, accuracy, and compliance with cGMP requirements, SOPs, and internal quality standards.
  • Verify that critical manufacturing steps, in-process inspections, reconciliations, and production documentation have been completed accurately.
  • Identify documentation discrepancies, omissions, or errors and coordinate timely resolution with Manufacturing and Quality teams.
  • Support product disposition activities by assessing batch documentation and escalating quality concerns as needed.
  • Retrieve production batch records for review and return completed documentation following approval.
  • Scan, organize, and maintain batch records in accordance with documentation and data integrity requirements.
  • Assist with investigations involving deviations, nonconformances, and Corrective and Preventive Actions (CAPAs) related to production documentation.
  • Verify identification and status labeling of raw materials, intermediates, and in-process materials.
  • Conduct inspections of manufacturing equipment, production areas, and materials to ensure compliance with quality standards.
  • Support inventory status control activities, including quarantine, approved, and rejected materials.
  • Assist with facility compliance activities, including pest control program support and vendor documentation review.
  • Provide guidance to production personnel on proper batch record documentation practices.
  • Participate in continuous improvement initiatives to enhance quality processes and regulatory compliance.
  • Maintain organized quality documentation and perform additional Quality Assurance responsibilities as assigned.

Job Requirements

  • Minimum of 1–3 years of Quality Assurance experience in a pharmaceutical, biotechnology, medical device, or other regulated manufacturing environment.
  • Associate degree in a scientific, technical, or related discipline required.
  • Experience performing end-of-process Quality Assurance activities; Quality Control experience alone is not sufficient.
  • Experience reviewing and scanning manufacturing batch records.
  • Working knowledge of current Good Manufacturing Practices (cGMP).
  • Proficiency with Microsoft Word and Excel.
  • Strong attention to detail and documentation accuracy.
  • Excellent organizational, verbal, and written communication skills.
  • Ability to manage multiple priorities and meet deadlines.

Education

  • Associate degree in a scientific, technical, or related discipline required.

Work Experience

  • 1–3 years of experience in Quality Assurance within a regulated manufacturing environment.
  • Previous batch record review experience in pharmaceutical manufacturing preferred.
  • Experience supporting deviations, CAPAs, investigations, or quality systems preferred.
  • Familiarity with FDA-regulated manufacturing environments and data integrity principles preferred. #ZR
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About Equiliem

Sourced by ZipRecruiter

Equiliem specializes in staffing clinical, non-clinical, and allied personnel. We excel in all levels, disciplines, and specialties within the healthcare spectrum. Our projects range from short to long term local and travel assignments. Equiliem has been recognized as a certified small business enterprise. In addition, we are proud that we have earned the prestigious Joint Commission accreditation for staffing firms and have been awarded Best in Staffing 4 years running by our employees and client partners.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

East Brunswick, NJ, US

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