Overview
Job Description
Job Title: QA Investigation WriterLocation: Greenville, NCPay: $40 - $50/hr on W2
Job Summary: Seeking a QA professional with strong hands-on experience writing investigation reports in pharmaceutical or biotechnology GMP environments.
Responsibilities:
- Author clear, thorough deviation, OOS/OOT, and manufacturing investigation reports.
- Conduct root-cause analysis using tools such as 5 Whys and Fishbone.
- Document product-impact assessments, develop CAPAs, and support timely investigation closure.
- Collaborate with Manufacturing, QC, Engineering, and QA to gather evidence and ensure inspection-ready documentation.
Requirements:
- Proven experience independently writing and closing GMP investigations.
- Strong technical writing, analytical, and communication skills.
- Experience with TrackWise, Veeva, or similar quality systems preferred.
Contact to Apply:Name: Uzma Kousar MohammedEmail:
uzma.kousar@intellectt.com
Phone:732-993-4997INTELLECTT INCBenefits: Eligible employees may have access to benefits offered by Intellectt Inc. in accordance with the applicable benefit plans and eligibility requirements.
Equal Employment Opportunity: Intellectt Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local law.
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