Careers

Document Control Training Coordinator

Job Title
Document Control Training Coordinator
Job ID
27387220
Location
Wheeling,  IL 60090
Other Location
Description

Document Control Training Coordinator, Wheeling, IL.

We’re hiring for a Document Control Training Coordinator to join our Quality Assurance Department at our Wheeling, IL. facility.

Job Description:  Document Control Training Coordinator will maintain the quality system requirements for medical device manufacturers according to ISO 13485 and FD 21 CFR 820. The Document Control Training Coordinator will be responsible for managing the Facility Document Control and Training programs. They will also support facility calibration, record retention, and internal audit programs.

The Document Control Training coordinator must have excellent attention to detail, strong problem-solving skills, and be able to interact with multiple facility functional areas in a very dynamic work environment. You will be responsible for maintaining customer requirements along with facility quality objectives and coordinates their implementation with functional areas such as Production, Engineering, Facilities Management, and Quality Assurance.

Document Control Training Coordinator​ Education and Experience Requirements:

  • Minimum Associates Degree in Science or appropriate industry experience
  • 3 years minimum experience in Good Manufacturing Practice (GMP) environment with ISO 13485 or ISO 9001 facility certification and a strong knowledge base of quality inspections and regulatory requirements.
  • Document Control and Training Coordination Experience 
  • ASQ certification such as a Certified Quality Engineer or Certified Quality Auditor is preferred
  • Microsoft Excel, Microsoft PowerPoint, Calibration Recall, Calibration Manager, QAD
  • Supports ISO 13485 Recertification/Surveillance, FDA 21 CFR 820, and Customer Audits.                                                                                   

The Document Control Training Coordinator must be compliant to ISO 13485 and 21CFR820, Internal and Corporate Procedures. They will also be able to make sound judgment and be autonomous in some decision making with minimal supervision. This individual will Support Lean Six Sigma, Road to World Class Program, Continuous Improvement, and New Product Development. They will also Communicate with Production, Engineering, and Quality Manager promptly to address issues or foster continuous improvement for ongoing projects.

Argon Medical is a global manufacturer of specialty medical products, including a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology, and Oncology. With over 800 employees worldwide. Argon has manufacturing facilities located in Athens, TX, Wheeling, IL and Rochester, NY. Argon’s brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. https://www.argonmedical.com/about/our-company

If you are interested in hearing more about this Document Control Training Coordinator, contact a recruiter today at glenn.arrowood@argonmedical.com or apply online www.argonmedicaljobs.com.

Required Skills

Minimum Associates Degree in Science or appropriate industry experience
3 years minimum experience in Good Manufacturing Practice (GMP) environment with ISO 13485 or ISO 9001 facility certification and a strong knowledge base of quality inspections and regulatory requirements.
Document Control and Training Coordination Experience
ASQ certification such as a Certified Quality Engineer or Certified Quality Auditor is preferred
Microsoft Excel, Microsoft PowerPoint, Calibration Recall, Calibration Manager, QAD
Supports ISO 13485 Recertification/Surveillance, FDA 21 CFR 820, and Customer Audits.

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