Quality Engineering Intern

Overview

This position is a 16-week paid co-op internship located in Bloomington, Indiana. It is offered for a period extending from January 2026 through April 2026. This position includes 401(k) options, an assigned mentor, capstone presentation, and intern events. If working onsite, you will also have access to a fitness center, an onsite cafeteria option, and a one-time housing stipend. All internships provide hands-on experience with meaningful projects in the Medical Device Manufacturing Industry.

Responsibilities

• Drive Continuous Improvement: Facilitate, lead, and collaborate with cross-functional teams, including Quality, Engineering, and Production, to identify and implement quality improvement initiatives. 

• Project Leadership: Lead projects from inception to completion, including developing, monitoring, and reporting key performance metrics to track progress and demonstrate impact. 

• Quality Standards Compliance: Perform all tasks in alignment with internal and external quality standards, ensuring adherence to FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements. 

• Change Management: Initiate and drive change requests, ensuring thorough documentation and effective communication across relevant stakeholders. 

• Risk Assessments: Participate in risk assessments and failure mode effects analysis (FMEA) to identify potential quality issues and develop mitigation strategies. 

• Conflict Resolution: Address and resolve conflicts related to technical situations, fostering a collaborative environment for problem-solving. 

• Quality Management System: Adhere to and support the Quality Management System processes, contributing to its continuous improvement. 

• Collaboration and Communication: Work effectively and professionally with colleagues across various levels of the global organization, maintaining strong working relationships. 

• Safety Compliance: Strictly adhere to safety requirements, promoting a safe working environment for all team members. 

• Attendance and Standards: Maintain regular and punctual attendance while upholding company quality and productivity standards. 

• Adaptability: Remain calm and receptive in fast-paced situations, demonstrating flexibility and resilience in the face of changing priorities. 

What We Offer: 

• Opportunity to gain hands-on experience in a global medical device company. 

• Mentorship from experienced professionals in the field of quality engineering. 

• A collaborative and innovative work environment that encourages personal and professional growth. 

Join us for a spring co-op that provides invaluable experience and the chance to make a meaningful impact on global quality improvement projects at Cook Medical!

Qualifications

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, and Outlook) is required. 

• Strong organizational skills with the ability to manage multiple projects and tasks simultaneously. 

• Critical thinking and meticulous attention to detail are essential for analyzing data and producing accurate reports. 

• Excellent verbal and written communication skills, including technical writing, to convey complex information clearly and effectively. 

• Previous experience in a quality engineering or manufacturing environment is a plus but not required. 

• All candidates should have an interest in a career in the Life Sciences field, a willingness to take initiative, and an ability to work well with others 

• Candidates should be students entering their Junior or Senior year the following fall semester or entering graduate school

• A minimum GPA of 3.0 is preferred 

• All candidates must provide proof of enrollment (including pre-registration certification for the following fall) for consideration 

• Multiple disciplines will be considered (e.g., Marketing, Life Sciences, General Business, and Management)  

Preferred Qualifications:

• Enrollment in a Bachelor’s or Master’s degree program in Engineering, Quality Assurance, or a related field, with a focus on quality systems or regulatory compliance. 

• Familiarity with quality improvement methodologies (e.g., Six Sigma, Lean) andd PowerBI is highly desirable. 

• Understanding of risk management principles and experience with risk assessment tools.