CMC Regulatory Data Science Co-Op — Hybrid Dashboards & Reports

Boehringer Ingelheim GmbH; Ridgefield (CT); Hybrid; USD 33,000 - 45,000; Full time

Benefits offered by this job

Housing stipend

Job summary

Boehringer Ingelheim is seeking a Data Science co-op to join our CMC Regulatory Affairs team at the Ridgefield facility. You will optimize data platforms, build reports and dashboards, and ensure regulatory needs are met through data-driven solutions.

The role is hybrid, requiring 2 days on-site in Ridgefield, CT, and offers exposure to global regulatory data platforms within a leading pharmaceutical environment.

Qualifications

• Must be a current graduate degree student in good academic standing.
• Student must be enrolled at a college or university for the duration of the internship.
• GPA 3.0 on a 4.0 scale preferred.
• Major or minor in related field of internship.
• Undergraduate students must have completed at least 12 credit hours.
• Graduate students must have completed at least 9 credit hours.
• For students on a work visa, pre-approved visa through current college and eligibility to work 40 hours/week for six months or more.

Responsibilities

• Optimize current data platforms for report generation.
• Use PowerApps to develop relevant reports.
• Evaluate regulations to ensure reports meet regulatory needs.
• Optimize CMC databases and tracking tools using existing software.
• Create dashboards for CMC submission metrics and information databases.

Skills

Data analysis

Planning & organization

Problem solving

Verbal & written communication

Team collaboration

Attention to detail

Education

Degree in Computer Science / Data Management / related field

Graduate student status

Tools

PowerApps

SQL / Databases

Job description

Boehringer Ingelheim is seeking a Data Science co-op to join our CMC Regulatory Affairs team at the Ridgefield facility. You will optimize data platforms, build reports and dashboards, and ensure regulatory needs are met through data-driven solutions.

The role is hybrid, requiring 2 days on-site in Ridgefield, CT, and offers exposure to global regulatory data platforms within a leading pharmaceutical environment.