CMC Intern: Pharma Regulatory & Data Analysis

Xeris Pharmaceuticals, Inc.; Chicago (IL); On-site; USD 33,000 - 36,000; Full time

Job summary

Xeris Pharmaceuticals, Inc. in Chicago offers a Chemistry Manufacturing and Controls (CMC) internship to support regulatory and development activities.

You will gain exposure to FDA/USP guidance, assist with study design, data analysis, and regulatory documentation within a collaborative team environment. The internship is onsite, five days per week, with an hourly wage of $24.00–$26.00, and aims to develop professional skills through a final internship presentation and comprehensive

Qualifications

• Pursuing a Bachelor’s or graduate degree in Biology, Chemistry, Chemical Engineering, Biochemical Engineering or related field.
• Minimum GPA 3.0.
• Returning to academic program for at least one semester post-internship.
• Prior classes in introductory chemistry, as well as organic chemistry and/or analytical chemistry.
• Strong verbal and written communication skills.

Responsibilities

• Research guidance from FDA and USP to understand technical requirements for product development and ongoing product support.
• Assist with preparing and reviewing study designs, data trend analysis, summary reports, risk assessments, and regulatory documentation.
• Support the team in day-to-day operations as needed.
• Participate in team meetings and contribute ideas.
• Collaborate with cross-functional teams as needed.
• Prepare a comprehensive review of the internship experience and present to the organization at the end of the internship.

Skills

Written and Verbal Communication

Teamwork

Attention to Detail

Self-Starter

Analytical Skills

Problem Solving

Organizational Skills

Adaptability

Professionalism

Microsoft Office

Education

Bachelor’s or graduate degree in Biology, Chemistry, Chemical Engineering, Biochemical Engineering or related field

Tools

Microsoft Office

Job description

Xeris Pharmaceuticals, Inc. in Chicago offers a Chemistry Manufacturing and Controls (CMC) internship to support regulatory and development activities.

You will gain exposure to FDA/USP guidance, assist with study design, data analysis, and regulatory documentation within a collaborative team environment. The internship is onsite, five days per week, with an hourly wage of $24.00–$26.00, and aims to develop professional skills through a final internship presentation and comprehensive