Document Control Coordinator

Company 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

Job Description

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

Additional Information

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