Quality Engineer Development Program - Summer 2027 Start

Medline Industries, Inc. in; Northfield Township (IL); On-site; USD 67,000 - 101,000; Full time

Benefits offered by this job

Health insurance

401(k) contributions

Paid time off

Job summary

Medline Industries, LP invites motivated early-career candidates to join its Quality Engineer Development Program. This two-year program begins with HIT and includes rotations across Corporate Divisional and Manufacturing Quality roles to build a strong foundation in Quality engineering.

Participants will work on device master records, design controls, risk management, and CAPA processes while contributing to cross-functional teams and regulatory compliance.

Qualifications

• Pursuing a bachelor's degree in science, engineering, or other related major.
• 3.0 minimum GPA preferred.
• Experience processing details and prioritizing importance to problem solve.
• Experience using time management skills across multiple projects with deadlines.
• Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook).
• Unrestricted permanent US work authorization.

Responsibilities

• Provide Quality support throughout the product lifecycle from design to post-market surveillance.
• Author Device Master Records, Design Controls, Risk Management, protocols and reports in compliance with regulations.
• Develop test plans to evaluate new and existing products.
• Collaborate with Regulatory, R&D, Product Managers, Manufacturing and other functions.
• Investigate, track and trend complaints and generate trend/Management Review reports.
• Communicate significant QA issues and recommend process improvements to management.
• Engage in process improvement related to product quality and regulatory compliance.
• Support CAPA's, SCAR's, supplier maintenance, and more.

Skills

Detail orientation

Time management

Problem solving

Education

Bachelor's degree in science or engineering

Tools

MS Office Suite

Job description

Quality Engineer Development Program - Summer 2027 Start (Biotech)

Job Summary

With more than 50 years of consecutive growth, we've built a dynamic workplace where over 45,000 employees worldwide are empowered to grow and contribute to our entrepreneurial culture. As we continue to grow, we're looking for talented individuals, like you, to join our team. Our people are genuine, creative, and proactive problem-solvers who move fast, move mountains, and succeed together.

Medline offers early-in-career candidates a range of benefits and experiences that support both personal and professional growth, including recognition programs, employee resource groups, volunteer opportunities, Employee Appreciation Week, competitive healthcare benefits, and more.

The goal of the Quality Engineer Development Program is to build a strong foundation in Quality by providing employees with the knowledge, tools, and experiences they will need to be a successful Quality Engineer at Medline. This two-year program starts with 12 weeks of High Intensity Training (HIT), which includes eLearnings, Instructor-Led Trainings, and real-world assignments so that employees can make an impact while they learn. After HIT, employees will be assigned to a Divisional Corporate Quality role for 9 months, followed by a 12-month rotation in a Manufacturing Quality role at one of our domestic manufacturing sites. While in these rotations, they will take ownership of a variety of product lines and projects to reinforce and challenge lessons learned during HIT. We strive to prepare employees to be a successful Quality Engineer at Medline by providing a broad, holistic set of training and experiences in both Corporate Divisional and Manufacturing Quality roles.

Upon successful completion of the two-year Quality Engineer Development Program, our goal is for employees to move into a Quality Engineer level role that best suits their interests and aligns with Medline's business needs.

Job Description

The challenging responsibilities of the position include:

• Providing Quality support throughout the lifetime of a product from design, to launch, to post-market surveillance
• Authoring Device Master Records, Design Controls, Risk Management, protocols, reports, and other critical Quality documentation in compliance with applicable regulations
• Developing test plans to evaluate new and existing products
• Collaborate with Regulatory, R&D, Product Managers, Manufacturing, Operations, and other cross functional groups
• Investigate, track, and trend customer and sales force complaints, including generation of trend and Management Review reports
• Communicate significant issues or developments identified during quality assurance activities and provide recommended process improvements to management
• Engaging in process improvement activities related to product quality and regulatory compliance
• Supporting CAPA's, SCAR's, supplier maintenance, and more!

Qualifications:

• Pursuing a bachelor's degree in science, engineering, or other related major
• 3.0 minimum GPA preferred
• Experience in processing details and understanding and prioritizing their importance to problem solve and draw clear and concise conclusions
• Experience using time management skills such as prioritizing/organizing and tracking details and meeting deadlines of multiple projects with varying completion dates
• Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook).
• Unrestricted permanent US work authorization

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The anticipated salary range for this position:

$67,000.00 - $101,000.00 Annual

The actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here .

We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging pagehere .

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

Salary Minimum: 74000Salary Maximum: 74000