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Document Control Specialist

Job in Huntley, McHenry County, Illinois, 60142, USA
Listing for: Life Spine
Full Time position
Listed on 2026-07-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 50000 - 70000 USD Yearly USD 50000.00 70000.00 YEAR
Job Description & How to Apply Below

Life Spine is focused on providing innovative solutions to address spinal pathology from the occiput to the sacrum. Our comprehensive product portfolio that centers around fusion and minimally invasive surgeries is driven by patient and surgeon needs. We are dedicated to improving the quality of life for patients by increasing procedural efficiency and efficacy through innovative design, uncompromising quality standards and the most technologically advanced manufacturing platforms.

We are looking for responsive, customer centric innovators to provide solutions for spinal pathology.

The Document Control Specialist is responsible to maintain, create, and modify all documents in a compliant and efficient manner for training, auditing, and compliance purposes across all departments. The primary purpose of this position is to perform and serve as the primary document and records coordinator who will manage the workflow of internal and external documents including document management, system and process documentation, and document storage (electronic and physical).

Duties

and Responsibilities
  • Manage and move approved documents to the controlled drive
  • Ensure appropriate signatures on all controlled documents for files
  • Log and file engineering change orders
  • Create new part numbers in the log and ERP system
  • Create UDI and keep updated in the GUDID
  • Create and maintain Product Labels
  • Perform regular document audits for accuracy and relevance
  • Scan and maintain Design History files
  • Maintain RA/QA Procedural Training
  • Participate and conduct regular quality audits
  • Maintain Distributor portal
  • All other duties as assigned
Qualifications

Minimum qualifications: Bachelor’s degree with a minimum of two years working in a quality environment. Familiar with mechanical drawings, blueprint reading, statistics, and sampling, preferred. Experience and knowledge of medical device Quality System Regulations and ISO Standards. Experience with 510(k) and CE preferred.

Essential Experience and Skills
  • Quality orientation and high attention to detail.
  • Excellent interpersonal and communication skills.
  • Experience working with high performance teams.
  • Problem analysis and problem resolution skills.
  • General knowledge of manufacturing processes.
Physical Demands

Sedentary work. Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Must be able to sit for long periods of time.

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