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Data entry, Quality Assurance - QA​/QC

Job in New York, New York County, New York, 10261, USA
Listing for: Green Key Resources
Full Time position
Listed on 2026-07-18
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Data Analyst, QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 42000 - 64000 USD Yearly USD 42000.00 64000.00 YEAR
Job Description & How to Apply Below
Position: Data Entry Support
Location: New York

The client is seeking a highly accurate, detail-oriented Data Entry Support to join their team. In this contract, full-time role, you will be responsible for transferring, updating, and verifying large volumes of information across our internal systems. You will play a vital role in maintaining data integrity and supporting Quality Management System (QMS) activities within a GMP-regulated environment. This role will work closely with Quality consultants and requires experience with GMP quality processes including Deviations, CAPAs, Change Control, and Vendor Management.

Required experience working within a GMP Quality Management System (QMS), including hands-on experience with Deviations, CAPAs, Change Control, and Vendor Management processes.

Primary Responsibilities Data Input
  • Efficiently transcribe information from emails and attachments to our ZenQMS system or a spreadsheet.
Quality Assurance
  • Verify data for accuracy, completeness, and consistency prior to entry. Identify and correct discrepancies or inconsistencies in existing records.
Quality Systems Support
  • Accurately enter, maintain, and update GMP quality records within ZenQMS.
  • Support the management and tracking of Deviations, CAPAs, Change Controls, and Vendor Management documentation.
  • Collaborate closely with Quality consultants to ensure quality records are complete, accurate, and compliant with internal procedures and regulatory requirements.
Compliance & Security
  • Handle confidential and sensitive company/customer information strictly in accordance with data protection protocols.
Required

Skills and Qualifications
  • Strong GMP Quality Management System (QMS) experience is required.
  • 3 to 5 years of experience in data entry, quality systems administration, or document management within a GMP-regulated pharmaceutical, biotechnology, medical device, or life sciences environment.
  • Strong computer skills with a high level of proficiency using Microsoft 365 (especially Excel) and cloud-based systems
  • Typing speed of 85 to 100 wpm with 99% - 100% accuracy, a meticulous eye for detail to ensure data integrity and prevent costly errors
  • Excellent organizational skills with the ability to manage time efficiently in a deadline-driven environment
  • Strong analytical problem-solving skills, with the ability to elevate issues to the correct downstream collaborators
  • Clear verbal and written communication skills to liaise with team members and clarify data requirements
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