Jobs and Careers

Intern, Quality Control

United Statesfull_timeVerifiedPosted 6 Apr 2026

💰 $40,000/yr

About the role

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.    Potential Key Learning Areas:

  GMP Documentation Practices:

Understanding good documentation practices (GDP), completing logbooks, reviewing test records, and learning the structure of controlled documents such as SOPs, test methods, and forms.

Quality System Fundamentals:

Exposure to electronic systems including LIMS, training systems, document control platforms, and deviation/event tracking systems.

QC Testing Processes:

Observing analytical techniques commonly used in biologics QC, such as HPLC/UPLC, spectrophotometry, endotoxin testing, osmolality, pH, and appearance.

Sample and Material Management:

Understanding chain-of-custody, sample receipt, labeling, storage conditions, and inventory practices.

Qualifications: 

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.

Interest in biopharmaceutical development, CMC processes, or project management preferred.

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.

Position Type/Expected Hours of Work:        This role is a temporary position operating Monday through Friday, 5x8 (5 days x 8 hours) schedule. 
Internship to begin on Monday, June 15th and end on Friday, August 21st.    What to Expect as an Avid Bio Intern:   

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.