Medline Industries
Job Opportunity
This position is available in Northfield, Illinois and offers a hybrid remote work option. The role is full-time and was posted today. Job Summary
The role involves managing development and implementation of methods and procedures for process control, validation, improvement, testing, and inspection to ensure product functionality. It also includes designing experiments to understand sources of variation affecting products and processes, and applying statistical process control methods for data analysis. Major Responsibilities
Manage development and implementation of methods and procedures for process control, process validation, process improvement, testing, and inspection. Design experiments to understand sources of variation affecting products and processes. Apply statistical process control methods for analyzing data. Design and perform experimental product testing and analysis to maintain quality levels and minimize defects and failure rates. Direct and collaborate with supplier representatives on quality issues, ensure corrective action implementation, and contribute to supplier quality improvement programs. Provide Quality expertise in Product Development, Design Control activities, Risk Management, and CE Technical Files. Build appropriate product documentation in compliance with applicable regulations. Work with Regulatory Groups and Suppliers to produce 510K submissions, letters to file, etc. Coordinate product testing with internal and external laboratories as required. Ensure compliance with domestic and international regulations associated with product lines and processes. Perform quality reviews of design documentation. Lead investigations of product and process non-conformances and out-of-specification results and develop effective corrective and preventive actions. Education
Typically requires a Bachelor's degree in Engineering, Science, Math or other related technical field. Work Experience
At least 2 years of experience in the Quality or Engineering. Knowledge / Skills / Abilities
Experience developing ways of accomplishing goals with little or no supervision. Experience using time management skills to prioritize, organize, and track details. Experience problem solving, overcoming obstacles, and reaching a positive and successful solution. Experience using MS Office Suite products. Intermediate Skill Level in Microsoft Excel. Working knowledge of government and industry quality assurance codes and standards. Position requires up to 15% travel. Preferred Job Requirements
At least 2 years of industry experience in Medical Devices, Drugs, and/or fields directly related to the role. 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: $79,560.00 - $115,440.00 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 as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. 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. 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.
This position is available in Northfield, Illinois and offers a hybrid remote work option. The role is full-time and was posted today. Job Summary
The role involves managing development and implementation of methods and procedures for process control, validation, improvement, testing, and inspection to ensure product functionality. It also includes designing experiments to understand sources of variation affecting products and processes, and applying statistical process control methods for data analysis. Major Responsibilities
Manage development and implementation of methods and procedures for process control, process validation, process improvement, testing, and inspection. Design experiments to understand sources of variation affecting products and processes. Apply statistical process control methods for analyzing data. Design and perform experimental product testing and analysis to maintain quality levels and minimize defects and failure rates. Direct and collaborate with supplier representatives on quality issues, ensure corrective action implementation, and contribute to supplier quality improvement programs. Provide Quality expertise in Product Development, Design Control activities, Risk Management, and CE Technical Files. Build appropriate product documentation in compliance with applicable regulations. Work with Regulatory Groups and Suppliers to produce 510K submissions, letters to file, etc. Coordinate product testing with internal and external laboratories as required. Ensure compliance with domestic and international regulations associated with product lines and processes. Perform quality reviews of design documentation. Lead investigations of product and process non-conformances and out-of-specification results and develop effective corrective and preventive actions. Education
Typically requires a Bachelor's degree in Engineering, Science, Math or other related technical field. Work Experience
At least 2 years of experience in the Quality or Engineering. Knowledge / Skills / Abilities
Experience developing ways of accomplishing goals with little or no supervision. Experience using time management skills to prioritize, organize, and track details. Experience problem solving, overcoming obstacles, and reaching a positive and successful solution. Experience using MS Office Suite products. Intermediate Skill Level in Microsoft Excel. Working knowledge of government and industry quality assurance codes and standards. Position requires up to 15% travel. Preferred Job Requirements
At least 2 years of industry experience in Medical Devices, Drugs, and/or fields directly related to the role. 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: $79,560.00 - $115,440.00 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 as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. 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. 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.