Co-op: Global Quality & Regulatory Data Automation

Regulatory Jobs; Madison (NJ); On-site; USD 39,000 - 41,000; Full time

Job summary

Bristol Myers Squibb in Madison, NJ offers a co-op with the Global Quality - Commercial Specification Committee. You will help build digital tools to automate JoS reviews, analyze regulatory inputs, and support automation across CSC.

This internship develops skills in regulatory science, data analytics, and cross-functional teamwork. The role emphasizes compliance with ICH standards and Health Authority precedents, with a focus on quality and patient safety.

Qualifications

• Currently enrolled in a Bachelor's degree program with GPA ≥3.0
• Pursuing CS, Data Science, Regulatory Affairs or Digital/Tech
• Strong analytical and data skills (Python, Excel)
• Excellent written and verbal communication
• Authorized to work in the US for duration of employment

Responsibilities

• Design & build digital tools to automate JoS review workflows
• Define logic and criteria the tool uses to assess specifications
• Test tools against JoS packages and align outputs with Health Authority precedents
• Maintain a structured knowledge repository of HA queries and responses
• Develop dashboards and trackers to monitor CSC activities
• Automate Specification Proposal and JoS templates to pre-populate data fields

Skills

Python

Excel

Data analysis

Education

Bachelor's degree in CS/Data Science/Regulatory Affairs or related

Tools

SharePoint

Job description

Bristol Myers Squibb in Madison, NJ offers a co-op with the Global Quality - Commercial Specification Committee. You will help build digital tools to automate JoS reviews, analyze regulatory inputs, and support automation across CSC.

This internship develops skills in regulatory science, data analytics, and cross-functional teamwork. The role emphasizes compliance with ICH standards and Health Authority precedents, with a focus on quality and patient safety.