Demo

Document Control Coordinator

Integrated Resources, Inc ( IRI )
Miami, FL Contractor
POSTED ON 1/8/2026
AVAILABLE BEFORE 4/5/2026

Job Description: Monday-Friday 8am - 5pm Fully on site


About the Role

As a Technical Documentation Coordinator Contractor, you will create, format, and coordinate the approval and implementation of labeling documents and reagent and consumable instructions for use documents.


Responsibilities

  • Editing and proofing of English and multilingual Reagent IFU documents.
  • Ensure reagent and instrument labeling documents are created, updated and in compliance with company standards, ISO and GMP as required.
  • Creation and maintenance of documentation and illustrations that are used by analytical systems.
  • Creation and revision of product labels using Adobe Illustrator or similar graphic tools.
  • Implementation of Design Changes to labeling; release change in compliance with company standards.
  • Work with multifunctional teams including Regulatory Affairs, Technical Support and Manufacturing to complete day to day activities.
  • Query business systems for company information to complete the project documentation.
  • Follow company process and procedures to schedule and project from draft through approval and release.
  • Participates in team meetings.


Qualifications

  • Bachelor’s Degree preferred with 0-2 years of experience.


Required Skills

  • Proficient in Microsoft Office applications, Adobe Acrobat and other design tools such as Adobe Illustrator and Adobe Photoshop.
  • Demonstrated ability to operate independently, with initiative and good business judgment.
  • Excellent verbal and written communication skills including grammar.
  • Excellent organizational and follow-up skills, as well as great attention to detail.
  • Desire to work independently with minimum supervision.
  • Can work and communicate effectively with a variety of people and across functional groups.


Preferred Skills

  • Knowledge/Experience of medical device quality systems include FDA, GMP & ISO preferred.
  • Knowledge computer systems used in product development and manufacturing.
  • Ability to coordinate project activities with multiple groups and individuals.
  • Prioritize tasks and resolve routine issues.
  • Experience working with labels and multilingual documents.
  • Experience working in a fast-paced environment.

Salary : $29

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