Job Title Quality Documentation Review
Location Clayton, NC
Work Arrangement: Onsite
Possible/Commutable Locations: Clayton, Garner, Raleigh, Knightdale, Wendell, Zebulon, Wilson's Mills, Smithfield, and surrounding areas.
Candidates must be able to reliably commute to the Clayton, NC worksite.
Employment Type Temporary / Contract
Monday–Friday | 9:00 AM–3:00 PM
Saturday–Sunday: Off
Duration 12 Months
The listed pay range is provided in good faith based on the information available for this position. Actual compensation may vary within the stated range based on job-related qualifications, experience, skills, and applicable assignment terms.
Benefits
Contract position = no employer-provided benefits. Any benefits, if applicable, are subject to the staffing employer's applicable plan and eligibility requirements.
Job Summary
We are seeking a detail-oriented professional to support Quality Documentation Review activities associated with batch release and electronic batch records.
The selected candidate may support documentation review activities across Fractionation, Purification, Filling, or Packaging operations. Training will be provided on the applicable electronic documentation processes based on the assigned manufacturing area.
The position may also involve additional office-related activities as assigned by management.
Responsibilities
Required Qualifications
Preferred Qualifications
Work Requirements
Equal Opportunity Employer
We are an Equal Opportunity Employer. Employment decisions are based on qualifications, merit, business needs, and other lawful factors and are made without discrimination or harassment based on any characteristic protected by applicable federal, state, or local law.
Reasonable accommodations are available to qualified individuals with disabilities in accordance with applicable law.
Application
Qualified candidates are encouraged to submit an updated resume highlighting experience with quality documentation, electronic batch records, document review, batch-release support, Quality Assurance, Quality Control, pharmaceutical/biotechnology manufacturing, or other regulated environments.
Candidates with strong attention to detail and experience working with electronic documentation systems are encouraged to apply.
