Quality Systems Document Controller

Stryker; Irvine (CA); On-site; USD 37,000 - 49,000; Full time

Benefits offered by this job

Bonus eligible

Benefits

Job summary

Stryker Irvine, CA is seeking a Document Control Coordinator to support Operations, R&D, RA and QA by preparing, reviewing, routing, approving and archiving Quality System documents.

The role emphasizes change orders, file management, logs, and ensuring FDA/ISO 13485 compliance, with onsite first shift and start times between 8:00 AM and 5:00 PM; overtime may be required. Travel 0%.

Qualifications

• Minimum 2 years Document Control experience or 4-year college degree.
• Proficient in Microsoft Word.
• Strong writing and communication skills.
• Able to read, understand and relay technical information accurately and concisely.

Responsibilities

• Review change orders and related docs to ensure compliance with document and change control procedures.
• Manage hardcopy and digital Quality System files.
• Update and maintain Document Control logs.
• Guide companywide on Quality System and Document Control functions.
• Track and facilitate timely documentation review and implementation.

Skills

Document Control

Microsoft Word

Typing

Technical Writing

Reading Comprehension

Education

4-year college degree

Tools

Propel

MasterControl

NetSuite

Procurify

CAD (SolidWorks)

Job description

Stryker Irvine, CA is seeking a Document Control Coordinator to support Operations, R&D, RA and QA by preparing, reviewing, routing, approving and archiving Quality System documents.

The role emphasizes change orders, file management, logs, and ensuring FDA/ISO 13485 compliance, with onsite first shift and start times between 8:00 AM and 5:00 PM; overtime may be required. Travel 0%.