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Document Control Specialist

Job in Oneonta, Otsego County, New York, 13820, USA
Listing for: DivIHN
Full Time position
Listed on 2026-03-03
Job specializations:
  • Quality Assurance - QA/QC
  • Administrative/Clerical
Job Description & How to Apply Below
For further inquiries regarding the following opportunity, please contact one of our Talent Specialists:
Hari at

Ragavendar at

Title:
Document Control Specialist

Location:

Oneonta, N
Y

Duration: 4 Months (Potential for extension or conversion based on project needs)

Locals preferred; non-locals acceptable if willing to relocate at their own expense.

Description of Work:
  • Responsible for administration of quality management system documents and records required for Client Life Sciences processes.
  • Responsible for initiation of document changes, distributions, notifications and fulfilling internal and external document distribution.
  • Generates, reviews, and maintains quality system documents including procedures, work instructions, job aids, certificate of conformances, etc. in compliance with ISO 13485, ISO 9001, and 21 CFR 820 standards.
  • Initiates Change Controls and Document Change Requests to update procedures and processes.
  • Works within departments and with various departments to update processes and procedures.
  • Assists in managing the document review and retention processes.
  • Supports or leads continuous improvement initiatives for document control related processes.
  • Supports other Quality Assurance functions as needed (internal audit, CAPAs, etc.)
  • Other duties as required
Skills/Experience:
  • Previous experience using ETQ or other Document Management software preferred
  • Proficiency in Microsoft office
  • Experience in ISO 9001 or other Quality System standards
  • ISO 13485 and 21 CFR 820 Quality Management Systems knowledge highly preferred
  • Must be detail oriented and accurate in execution of work
  • Able to work well both independently and in a group setting
Top

Skills Required:

  • Proficient in Microsoft Office (Excel, Word, Outlook, etc.)
  • Hands-on experience with ISO 9001 and other Quality System standards (preferred)
  • Familiarity with ISO 13485 and 21 CFR 820 is highly preferred
  • Experience with ETQ or similar Document Management Software (preferred)
Requirements:
  • Associate's or Bachelor's degree with 2+ years' experience (manufacturing environment preferred).
  • Strong MS Office skills
    , familiarity with ETQ or any Document Management System
    .
Preferred:
Experience using Macros
, Share Point , and other Office applications
  • Interview Rounds:
    • Round 1:
      Video Interview
    • Round 2:
      Onsite Interview
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