Quality Engineer Development Program - Summer 2027 Start

Medline; Northfield Township (IL); Hybrid; USD 67,000 - 101,000; Full time

Benefits offered by this job

Competitive healthcare benefits

Employee Resource Groups

Volunteer opportunities

Recognition programs

Job summary

Medline is offering a Quality Engineer Development Program starting Summer 2027 in Northfield, IL. The two-year program combines HIT with rotations in Corporate and Manufacturing Quality to build a strong foundation in Quality engineering.

Participants gain hands-on experience across design, regulatory, and manufacturing environments while preparing for a dedicated Quality Engineer role within Medline. Hybrid work arrangement is available.

Qualifications

• Pursuing a bachelor's degree in science, engineering, or related major.
• GPA of 3.0+ preferred.
• Strong attention to detail and ability to prioritize multiple projects.
• Experience with MS Office products.

Responsibilities

• Provide Quality support throughout the product lifecycle from design to post-market surveillance.
• Author Device Master Records, Design Controls, Risk Management and other critical Quality documentation.
• Develop test plans to evaluate new and existing products.
• Collaborate with Regulatory, R&D, Product Managers, Manufacturing, Operations and cross-functional groups.
• Investigate, track, and trend customer and sales force complaints and generate trend/Management Review reports.
• Recommend process improvements to management.
• Support CAPAs, SCARs, supplier maintenance and related activities.

Skills

Detail oriented

Time management

Problem solving

Cross-functional collaboration

Education

Bachelor's degree in science/engineering

Tools

MS Office Suite

Job description

Quality Engineer Development Program - Summer 2027 Start# Medline Careers## Quality Engineer Development Program - Summer 2027 StartApply: Hybrid: Northfield, Illinois: University Recruiting: Full time: Posted Today: R2615800**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 authorizationMedline 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 AnnualThe 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 page here.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.