Associate Ii - Quality Assurance, Document Control

Catalent Biologics

Madison, WI, US
Administer document management system
Maintain gmp documentation
Manage physical and electronic storage
The Document Control Quality Assurance Associate is responsible for administering the Document Management System, making documents effective and distribution according to standard operating procedure

Job Summary

  • The Document Control Quality Assurance Associate is responsible for administering the Document Management System, making documents effective and distribution according to standard operating procedure.
  • This position also corresponds with customers to obtain document approval.
  • Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.

Matching Summary

The Document Control Quality Assurance Associate is responsible for administering the Document Management System, making documents effective and distribution according to standard operating procedure.

Skills & Requirements

Must-have

  • Administer Document Management System
  • Maintain GMP documentation
  • Manage physical and electronic storage
  • Scan and file executed records
  • Assure document integrity
  • Manage document retention room

Nice-to-have

  • Entrepreneurial team environment
  • Career development opportunities
  • Collaborate with document owners
  • Personal initiative
  • Dynamic pace
  • Meaningful work

Key Requirements

  • Bachelor's Degree with 1 year experience
  • Associate's Degree with 4 years experience
  • High School Diploma with 6 years experience
  • STEM discipline preferred
  • Attention to detail
  • Strong communication skills
  • Work independently or as part of a team
  • Comfortable using computer systems
  • Strong customer service skills

Work Rights

Not specified

Tailored Resume

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