Regulatory Document Qc Specialist

My name is Uzma Kousar Mohammed, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Regulatory Document QC Specialist based in Warren, NJ with one of our prestigious clients.

I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at

Job Title: Regulatory Document QC Specialist
Location: Warren, NJ Hybrid (3 Days Onsite / 2 Days Remote)
Duration: 3+ Months
Pay Rate: $25/hr - $30/hr W2
Industry: Pharmaceutical / Biotechnology

Job Description:
Our client is seeking a detail-oriented Regulatory Document QC Specialist to support the quality and accuracy of scientific and regulatory documentation.

Key Responsibilities:

• Perform QC reviews of regulatory and scientific documents.
• Cross-check data against source documentation.
• Review formatting, tables, references, and data presentation.
• Identify and communicate discrepancies and required corrections.
• Support regulatory documentation and publishing activities.

Required Skills:

• Bachelor's degree in a scientific or related discipline preferred.
• Strong attention to detail.
• Experience working with scientific/technical documents.
• Strong organizational and written communication skills.
• Regulatory or Pharma/Biotech experience preferred.

Preferred:

• Veeva experience.
• Regulatory documentation/publishing experience.

Benefits: 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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