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Document Control Coordinator

Trident Consulting IncSan Clemente, CA🇺🇸United StatesPosted 4 Sept 2026

Quick Overview

Seniority
Junior
Employment type
Contract
Work mode
On Site
Location
San Clemente, CA, United States
Posted
8 hours ago

Job Description

About Trident:
Trident Consulting is an award-winning IT/engineering staffing company founded in 2005 and headquartered in San Ramon, CA. We specialize in placing high-quality vetted technology

Some of our recent awards include:
2022, 2021, 2020 Inc. 5000 fastest-growing private companies in America
2022, 2021 SF Business Times 100 fastest-growing private companies in Bay Area

Trident Consulting is seeking a "Document Control Coordinator" for one of our clients in "San Clemente, CA" A global leader in business and technology services.

 

Role: Document Control Coordinator

Location: San Clemente, CA

Type: Contract – Onsite

Pay: $20 - $22/hr on W2(Inclusive all)

 

Description

  • This position is responsible for ensuring the document control and training systems are maintained and functioning in compliance with Clients procedures and external standards and regulations.
  • In addition to QA responsibilities, there will be other activities required that support Production and Product Development as needed.

Document Control

  • Administering the approved Document Control database system.
  • Provide support to all personnel for document control
  • Creating reports in the approved system for Management Review, Trending requests, etc.
  • Maintaining the document control and training modules within the approved system
  • Addressing quality system gaps within the document control system stemming from audits.

Training

  • Administering the approved Training database.
  • Provide support to all personnel for training
  • Monitor the status of the training process
  • Provide reports on the status of training
  • Coordinate group training when needed Design History Files
  • Working with project managers on compiling and maintaining the DHFs.

Required

  • Experience requires 0-2 years of related experience Knowledge, Skills, and Abilities
  • Must have excellent documentation skills
  • Attention to detail and accuracy a must
  • Medical device experience and working knowledge of QSR
  • Medical device complaint experience preferred
  • Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable
  • Team player, good written/oral communicator
  • Able to thrive in a small, entrepreneurial environment
  • Must be organized and able to coordinate activities with internal departments and outside vendors

Education: Bachelor’s degree, preferably in a science

All your information will be kept confidential according to EEO guidelines.

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