This position is a 12-week paid internship located in Bloomington, Indiana. It is offered for a period extending from mid-May through mid-August (exact dates depend on school calendars.) 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 summer internship 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; candidates who graduate the spring semester before this internship are also eligible
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) is highly desirable.
Understanding of risk management principles and experience with risk assessment tools.
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