Intern, Quality Control
About The Position
The Intern, Quality Control (QC) will support routine laboratory and documentation activities within a GMP‑regulated biopharmaceutical environment. This role provides hands‑on exposure to QC processes, laboratory operations, and quality systems essential for biologics manufacturing. The intern will work alongside QC analysts and leadership to gain practical experience with regulatory expectations, data integrity principles, and analytical testing workflows. Working closely with QC leadership, analysts, and continuous improvement project teams, the intern will support ongoing initiatives, contribute to process‑improvement activities, and learn how operational excellence is embedded into regulated laboratory environments. We're thrilled to provide a 10-week paid internship at our facility in Tustin, CA. As an intern, you'll dive deep into our team culture, take on significant projects, and play a vital role in our team's dynamics. This temporary, 40-hour per week office position is designed to offer you a wealth of experience and the chance to connect with professionals in the industry.
Requirements
- Current enrollment in a Bachelor’s or Master’s program in Life Sciences, Engineering, Business, or a related field.
- Ability to understand scientific and technical concepts related to biologics development (training provided).
- Passionate about a career in the biotech industry and looking to gain valuable experience through this internship.
- Strong organizational skills with attention to detail.
- Excellent written and verbal communication skills.
- Proficiency with Microsoft Office (Word, Excel, PowerPoint) and collaboration platforms (Teams, SharePoint).
- Ability to work in a team environment, manage multiple tasks, and meet deadlines.
- Availability to work full-time for the duration of the internship at our Tustin, CA facility.
- Authorization to work in the country where the internship is located.
Nice To Haves
- Interest in biopharmaceutical development, CMC processes, or project management preferred.
Responsibilities
- Support routine laboratory and documentation activities within a GMP‑regulated biopharmaceutical environment.
- Work alongside QC analysts and leadership.
- Support ongoing initiatives and contribute to process‑improvement activities.
Benefits
- Summer Project: Personalized project plan, complete with a pre-determined roadmap and week by week milestones that the intern will need to meet, ensuring clear expectations and measurable outcomes.
- Mentorship: Your manager and team will provide training, mentorship, and development opportunities.
- Weekly Check-ins and 1:1s: Conduct both on a weekly basis to ensure clear communication and support for our interns.
- Performance Assessments: Conduct mid and end of program performance assessments to be provided with constructive criticism and feedback to help you grow and succeed.
- State of the Art Facility: You’ll be working amongst the brightest minds in our world class facilities
- Internship Experiences: Intern Open House, Summer Leadership Series, Lunch & Learns, Intern Night Out, Site Tours, End of Program Presentation
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Number of Employees
101-250 employees
