Document Control Coordinator

ProKatchers LLC; Chaska (MN); On-site; USD 42,000 - 64,000; Full time

Job summary

ProKatchers LLC is seeking a documentation specialist to implement changes based on red-lines and format engineering documents per documentation standards. You will review all documentation for accuracy, completeness and consistency in content, format, files and authorizations.

Filing, scanning, copying and electronic notification and distribution of released documentation, with the ability to prioritize in a demanding environment and meet deadlines.

Qualifications

• 2-3 years of relevant experience.
• Prior experience with documentation of Life Science or Medical Device products.
• Graduate from a recognized QA program preferred.

Responsibilities

• Implement changes based on red-lines and format engineering documents per documentation standards.
• Review all documentation for accuracy, completeness and consistency in content, format, files and authorizations.
• Filing, scanning, copying and electronic notification and distribution of released documentation.
• Skilled at prioritizing in a demanding and fast paced environment while producing error free work and meeting required deadlines.
• Experience working with Electronic Document Management System.

Skills

Documentation

QA experience

Attention to detail

Education

Graduate from a recognized QA program

Tools

Electronic Document Management System

Job description

• Implement changes based on red-lines and format engineering documents per documentation standards.
• Review all documentation for accuracy, completeness and consistency in content, format, files and authorizations.
• Filing, scanning, copying and electronic notification and distribution of released documentation.
• Skilled at prioritizing in a demanding and fast paced environment while producing error free work and meeting required deadlines.
• Experience working with Electronic Document Management System.
• Previous experience working within a GMP manufacturing environment would be an asset.

Qualifications:

• 2-3 years of relevant experience
• Graduate from a recognized program in QA preferred.
• Prior experience with documentation of Life Science or Medical Device products.