Regulatory Document QC Specialist

United Pharma; New Jersey; On-site; USD 52,000 - 72,000; Full time

Job summary

United Pharma in New Jersey is seeking a detail-oriented junior Regulatory Document QC Specialist to help ensure accuracy and consistency across regulatory and scientific documents. Reporting to Regulatory Affairs, you will perform QC reviews and support publishing activities.

The role emphasizes meticulous data checking, strong written communication, and the ability to work with source documentation. Veeva experience is a plus; bachelor's degree in a science field is preferred.

Qualifications

• Bachelor’s degree in a scientific or related discipline preferred.
• Strong attention to detail and ability to work with scientific/technical documents.
• Regulatory or pharmaceutical/biotech experience preferred but not required.
• Veeva experience is a plus.

Responsibilities

• Perform QC reviews of regulatory and scientific documents.
• Cross-check data within regulatory documents against source documentation for accuracy and consistency.
• Review document formatting, tables, references, and data presentation.
• Identify and communicate discrepancies or required corrections.
• Support general regulatory documentation and publishing activities as needed.

Skills

Attention to detail

Organizational skills

Written communication

Education

Bachelor’s degree in a scientific or related discipline

Tools

Veeva

Job description

Job Description: Our client is seeking a detail-oriented Regulatory Document QC Specialist

This is a junior-level role focused on ensuring the accuracy and consistency of scientific and regulatory documentation.

Responsibilities:

• Perform QC reviews of regulatory and scientific documents.
• Cross-check data within regulatory documents against source documentation for accuracy and consistency.
• Review document formatting, tables, references, and data presentation.
• Identify and communicate discrepancies or required corrections.
• Support general regulatory documentation and publishing activities as needed.

Qualifications

• Bachelor’s degree in a scientific or related discipline preferred.
• Strong attention to detail and ability to work with scientific/technical documents.
• Regulatory or pharmaceutical/biotech experience preferred but not required.
• Veeva experience is a plus.
• Strong organizational and written communication skills.