Summer 2026 Internship: Quality Control, Biomedical - Exton, PA at DSM

Exton, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

06 Apr, 26

Salary

26.0

Posted On

06 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, Biomedical Engineering, Communication, Interpersonal Skills, Analytical Skills, Data Entry, Document Management, Problem-Solving, Organizational Skills, Flexibility, Continuous Improvement, Technical File Updates, Batch Record Reviews, ISO 13485 Compliance, Regulatory Affairs, Quality Systems, Data Analysis

Industry

Chemical Manufacturing

Description

Summer 2026 Internship: Quality Control, Biomedical Exton, PA If you’re looking to grow your network and gain new skills within a global company, an internship with dsm-firmenich could be the program for you. Our summer internships provide students opportunities to work on real business projects and gain invaluable professional experience. As an intern, you’ll have exposure to many different areas of a global flavors, fragrances, and ingredients organization that works with some of the biggest brands in the world, along with opportunities to network with your peers and leadership. From engaging events to mentoring opportunities and valuable resume-building experiences, we’re committed to preparing you for a fulfilling and enduring career, both at dsm-firmenich and beyond. We are currently looking for a “2026 Summer Internship: Quality Control, Biomedical” at our Biomedical facility in Exton, PA. The 2026 dsm-firmenich Summer Internship Program will run from June 1, 2026 to August 14, 2026. Working Hours: Monday – Friday, 8:00am – 5:00pm Join our Quality team as an intern and gain invaluable professional experience. Enhance your skills and contribute to real projects that have visibility across the business through a Summer internship. Come discover all we have to offer! Your Key Responsibilities: Assist with Quality Control activities, including basic inspections, testing, data entry, and documentation of nonconformances. Support Document Control and Quality System processes by managing document changes, organizing records, and helping maintain ISO 13485 compliant files. Contribute to Product Release and Regulatory tasks, such as batch record reviews, technical file updates, labelling checks, audit preparation, etc. Participate in Engineering projects, including data collection for investigations (CAPA/NCR), supplier performance tracking, and continuous improvement initiatives. We Bring: Opportunities for students to develop skills and expand their professional connections within a company where sustainability is not just a slogan but is at the core of our strategy and purpose. We strive to create inclusive communities within our organization where every employee is equally valued and respected, regardless of their background, beliefs, or identity. Additionally, we provide an environment that encourages curiosity and an open mindset, allowing for personal and professional growth. Together, we can learn from one another to drive progress and create a better future. Build Your Future Skills: Gain hands-on experience and develop practical skills that prepare you for a successful career. Expand Your Network: Connect with professionals and peers in a company where sustainability drives every decision and action. Thrive in an Inclusive Culture: Join a community that values and respects every individual—regardless of background, beliefs, or identity. Grow Through Curiosity: Work in an environment that encourages open-mindedness, learning, and collaboration to create a better future together. You Bring: Currently working on completion of a Bachelor’s degree in Biomedical Engineering or related field Must be available to work full-time on-site in Exton, PA beginning on June 1, 2026 and ending on August 14, 2026. Excellent communication and interpersonal skills Strong analytical skills and ability to synthesize and parse data Strong organizational, problem-solving, and analytical skills; able to manage priorities and workflow Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm The hourly rate for this position is $23.00 - $26.00 per hour. Compensation will be dependent on factors that include location, education, training, specific skills, and years of experience. At the end of this internship, you will: Practical understanding of medical device quality systems, including how ISO 13485 requirements translate into daily operations, documentation, audits, and compliance. Hands-on experience with quality tools and processes, such as inspections, nonconformance documentation, CAPA support, data analysis, and product release activities. Improved technical and professional skills, including root-cause thinking, document management, cross-functional communication, and use of quality software or inspection equipment. A clear understanding of career paths within Quality, with exposure to QC, QA, Supplier Quality, Regulatory Affairs, and Quality Engineering to inform future professional goals. About dsm-firmenich: At dsm-firmenich, we don’t just meet expectations – we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions – every single day. Whether it’s fragrance that helps you focus, alternative meat that’s better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you’re making a difference, we’ll make sure you’re growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They’re essential to our future. Because real progress only happens when we go beyond, together. Inclusion, belonging and equal opportunity statement: At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work – and that’s exactly the kind of culture we’re building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We’re proud to be an equal opportunity employer, and we’re serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we’re committed to reflecting the world we serve. We welcome candidates from all backgrounds — no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we’re here to help – just let us know what you need, and we’ll do everything we can to make it work. Agency statement: We’re managing this search directly at dsm-firmenich. If you’re applying as an individual, we’d love to hear from you. We’re not accepting agency submissions or proposals involving fees or commissions for this role.

Responsibilities

Assist with Quality Control activities and support Document Control and Quality System processes. Contribute to Product Release and Regulatory tasks while participating in Engineering projects.