Chemistry Manufacturing & Controls (CMC) Intern-Summer 2027

Xeris Pharmaceuticals Inc; Georgia; On-site; USD 33,000 - 36,000; Part time

Benefits offered by this job

Equity or long-term incentive awards

Paid time off benefits

401(k) retirement benefits

Job summary

Xeris Pharmaceuticals, Inc. in Chicago invites a motivated intern to join the Chemistry Manufacturing and Controls (CMC) team.

You will gain experience developing pharmaceutical products in line with regulatory requirements and contribute to real-world projects in a collaborative environment. Ideal candidates are pursuing a Bachelor’s or graduate degree in biology, chemistry, chemical engineering, or related fields, with at least two years of undergraduate study and strong communication skills.

Qualifications

• Pursuing a Bachelor’s or graduate degree in Biology, Chemistry, Chemical Engineering, Biochemical Engineering or related field.
• Minimum GPA 3.0.
• Strong communication and teamwork skills.

Responsibilities

• Research guidance from FDA and USP to understand requirements for product development and regulatory documentation.
• Assist with study designs, data trend analysis, and risk assessments.
• Prepare summaries and review regulatory documents.
• Contribute in team meetings and cross-functional collaborations.
• Present internship findings to the organization at the end of the program.

Skills

Verbal communication

Written communication

Teamwork

Independent work

MS Office

Education

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

Tools

Microsoft Office

Job description

Job Description: Job Purpose

We are seeking a motivated and enthusiastic intern to join our Chemistry Manufacturing and Controls (CMC) department, part of our Product Development and Technology Operations organization. This internship offers experience in developing pharmaceutical products in accordance with regulatory requirements, exposure to real-world projects, and an opportunity to develop professional skills in a collaborative environment.

Essential Job Functions

Research guidance from agencies such as 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 At the conclusion of the internship, prepare a comprehensive review of the internship experience and present to the organization

Skills and Qualifications

Currently pursuing a Bachelor’s or graduate degree in Biology, Chemistry, Chemical Engineering, Biochemical Engineering or related field, and has completed a minimum of 2 years of undergraduate studies Minimum GPA 3.0 Returning to academic program at a credentialed institution for at least one semester post-internship Strong interest in pharmaceuticals Excellent verbal and written communication skills Ability to work independently and as part of a team Proficiency in Microsoft Office (Word, Excel, Powerpoint) Prior classes in introductory chemistry, as well as organic chemistry and/or analytical chemistry Thrive in a fast-paced, diverse work environment Competencies: Written and Verbal Communication, Teamwork & Collaboration, Attention to Detail, Self-Starter, Analytical skills, Problem Solving, Organizational skills, Adaptability, Professionalism.

Working Conditions

This role is based in Xeris’ Chicago office and requires five days per week in the office. On-site requirement may change at management’s discretion. #LI-ONSITE The anticipated hourly wage for this position is $24.00 - $26.00. We are committed to offering competitive compensation. Starting pay is determined based on a variety of factors, including the role, job-related knowledge, skills, experience, education, internal equity, market data, and the location of the role, where applicable. Xeris Pharmaceuticals, Inc. (the “Company”) is an equal opportunity employer and does not discriminate based on race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. All qualified candidates are given equal opportunity and the Company’s employment selection decisions are based solely on job-related factors. NOTE: This job description is not intended to be all-inclusive. The employee may be required to perform other related duties as needed to meet the ongoing needs of the Company. The level of the position will be determined based on the selected candidate’s qualifications and experience. Final determination of the actual base salary offered depends on several factors, including but not limited to the candidate’s skills, experience, education, location, and business needs.

Employees are eligible for equity or long-term incentive awards, where applicable. Field Sales role employees are eligible for a quarterly commission structure. Non-Sales role employees are eligible for an annual bonus. The Company also offers a comprehensive benefits package that includes additional elements such as paid time off benefits, various health, vision, and dental insurance options, 401(k) retirement benefits and more for eligible employees. Details about these and other offerings will be provided at the time a conditional offer of employment is made. Candidates are always welcome to inquire about our compensation and benefits package during the interview process. Individuals hired as temporary employees, interns, and preceptors are not eligible for commissions, bonuses, and/or long-term incentive or equity awards. Eligibility for other benefits will be based on plan documents.

Accessibility & Reasonable Accommodations

If, because of a medical condition or disability, you require a reasonable accommodation or assistance to complete any part of the application process, please send an e-mail to [e-mail] and identify the type of accommodation or assistance you are requesting. Please include the job requisition number in your message. Please note if your request is not for this stated purpose, you will not receive a response to your email. Do not include any medical or health information in this email.

Xeris participates in E-Verify. E-Verify Participation Poster EEO is the Law EEO is the Law EEO is the Law Supplement EEO is the Law Supplement Pay Transparency Nondiscrimination Provision Pay Transparency Nondiscrimination Provision Xeris is a growth-oriented biopharmaceutical company committed to improving patient lives by developing and commercializing innovative products across a range of therapies. Xeris is headquartered in Chicago, Illinois and has a strong foundation built on proprietary formulation technologies and deep expertise in clinical development and commercialization.

Accessibility & Reasonable Accommodations

If, because of a medical condition or disability, you require a reasonable accommodation or assistance to complete any part of the application process, please send an e-mail to [e-mail] and identify the type of accommodation or assistance you are requesting. Please include the job requisition number in your message. Please note if your request is not for this stated purpose, you will not receive a response to your email. Do not include any medical or health information in this email.

Equal Employment Opportunity

Xeris Pharmaceuticals, Inc. (the “Company”) is an equal opportunity employer and does not discriminate based on race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. All qualified candidates are given equal opportunity and the Company’s employment selection decisions are based solely on job‐relevant factors.