Quality Control Inspector I

Medline International; Eagan (MN); On-site; USD 25,000 - 37,000; Full time

Benefits offered by this job

Health insurance

Life insurance

Disability insurance

401(k) contributions

Paid time off

Job summary

Medline Industries, LP on-site in Eagan, MN is hiring a Quality Control Inspector I. The role focuses on inspecting incoming, in-process, and finished products, reviewing records, and supporting investigation and CAPA activities to uphold quality and regulatory standards.

Ideal candidates will be detail-oriented with basic math skills and familiarity with GMP, GDP, ISO, or 21 CFR 820/210-211; no prior experience required. Salaried hourly range provided below.

Qualifications

• Typically requires High School Diploma or equivalent.
• No experience required.
• Ability to read, write, speak and understand English.

Responsibilities

• Perform incoming, in-process, and finished product inspections.
• Review DHRs, batch records, sterilization documentation for completeness and compliance.
• Support release activities for finished products and ensure quality documentation is complete.

Skills

English proficiency

Attention to detail

Basic math

Quality regulations knowledge

Education

High School diploma

Job description

Quality Control Inspector I# Medline Careers## Quality Control Inspector IApply: On-site: CORP - Eagan, MN ADC: Full time: Posted Today: R2620927**Job Summary**• The QC Inspector serves as a key quality presence on the clean room production floor, providing inspection support, reviewing quality records, assisting with investigations, and driving timely resolution of quality issues. This position contributes directly to product quality, regulatory compliance, and continuous improvement initiatives.**Job Description****MAJOR RESPONSIBILITIES:*** + Perform incoming, in-process, and finished product inspections using approved sampling plans and inspection methods. + Review Device History Records (DHRs), batch records, sterilization documentation, and manufacturing records for completeness and compliance. + Support release activities for finished products and ensure required quality documentation is complete and accurate. + Assist with investigations related to nonconformances, deviations, complaints, supplier issues, and corrective actions. + Support CAPA implementation, effectiveness verification, and follow-up activities. + Assist with validation and verification activities including process validation, test method validation, and sterilization-related studies. + Support supplier quality activities including receiving inspections, supplier issue tracking, and follow-up actions. + Maintain quality metrics and prepare reports used for management review and quality performance monitoring. + Assist during internal, customer, regulatory, and certification audits. + Comply with Standard Operating Procedures (SOPs), Quality Systems, OSHA guidelines, and Medline’s rules and regulations.**MINIMUM JOB REQUIREMENTS:****Education:*** + Typically requires High School Diploma or equivalent.**Certification / Licensure:*** + No experience required.**Work Experience:*** + None**Knowledge / Skills / Abilities:*** + Ability to read, write, speak and understand English. + Attention to details. + Vision abilities including close vision, distance vision, depth perception and ability to adjust focus. + Basic math skills including addition, subtraction and fractional to decimal conversions. + Position requires: + Working in hot and cold environments. + Sitting, walking or standing for prolonged periods, with frequent twisting and bending. + Working in PPE or company issued gowns for prolonged periods + Ability to lift up to 50 lbs. + Ability to prioritize quickly in a fast paced manufacturing environment. + Ability to process all relevant details, understanding and prioritizing their importance and drawing concise conclusions. + Basic computer skills. + Ability to apply basic knowledge of quality regulations such as GMP, GDP, ISO, or 21CFR 820, 210 - 211.**PREFERRED JOB REQUIREMENTS:****Education:*** + None**Certification / Licensure:*** + None**Work Experience:*** + Experience in a medical device or other FDA-regulated manufacturing environment + Experience working in a cleanroom (ISO Class 7/8 or similar) + Experience inspecting medical devices or components (incoming, in-process, or final)**Knowledge / Skills / Abilities:*** + NoneMedline 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:$18.50 - $26.75 HourlyThe actual salary will vary based on applicant’s location, education, experience, skills, and abilities. 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.