Document Controls Speclialst

Peoplelink Staffing
Boca Raton, FL
Job Description
Document Control Specialist to join a leading cosmetics and personal care manufacturing company in Boca Raton, FL. Maintain and control quality documentation, generate and support Certificates of Analysis (COAs), and ensure compliance with GMP, ISO 22716, FDA guidelines, and Good Documentation Practices (GDP).

Requirements

  • Associate or Bachelor's degree in Chemistry, Biology, Quality, or related field preferred
  • 2–5 years of experience in a GMP-regulated cosmetics, personal care, pharmaceutical, OTC, or food manufacturing environment
  • Experience with document control systems such as MasterControl, TrackWise, SharePoint, or similar
  • Experience supporting or generating Certificates of Analysis (COAs)
  • Experience reviewing batch records and production documentation
  • Strong understanding of GMP and Good Documentation Practices (GDP)
  • Ability to interpret testing results and compare against specifications
  • Strong organizational skills and high attention to detail
  • Ability to manage multiple priorities in a fast-paced environment

Benefits

  • Medical, Dental, Vision & Life insurance
  • 401k available after reaching hours worked requirement
  • Direct Deposit Programs
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