Document Coordinator Ii

Par Health

St. Louis, United States
Hybrid
Cgmp pharmaceutical business experience
Document management system proficiency
Batch record and label issuance
Par Health is seeking a Document Coordinator II to manage and control quality assurance documentation and labeling processes in compliance with industry standards. The role emphasizes teamwork, quality improvement, and attention to detail within a supportive corporate culture

Job Summary

  • The Document Coordinator II manages the entire lifecycle of controlled documents and product safety labels in accordance with company and regulatory guidelines.
  • This role involves printing, issuing, and reconciling labels and batch records for intermediate and finished manufactured products at the St. Louis Plant.
  • Candidates must actively participate in cGMP walkthroughs, internal and external audits, and assist in investigating unexpected quality events.

Matching Summary

Match Score: 85

Par Health is seeking a Document Coordinator II to manage and control quality assurance documentation and labeling processes in compliance with industry standards. The role emphasizes teamwork, quality improvement, and attention to detail within a supportive corporate culture.

Skills & Requirements

Must-have

  • cGMP pharmaceutical business experience
  • document management system proficiency
  • batch record and label issuance
  • quality assurance document control
  • regulatory compliance adherence

Nice-to-have

  • lead role in document management
  • training new employees
  • cross-functional team collaboration
  • process improvement initiatives
  • fast-paced environment adaptability

Key Requirements

  • High School Diploma or GED equivalent
  • 1 to 3 years related experience required
  • Experience in cGMP pharmaceutical business preferred

Work Rights

Not specified

Tailored Resume

Cover Letter