New · posted Nov 8
Medline · Medical Devices
Quality Control Inspector II (1st Shift)
- Neptune, NJ
- On-site
- Full-time
- Associate & Specialist
The role
Under minimal supervision, the QC Inspector II oversees quality projects, ensures compliance with Medline SOPs, and maintains product integrity at the distribution center. Responsibilities include investigating and documenting held finished goods, managing holds and releases, completing rework assignments, inspecting raw materials and finished goods using various methods, recording inspection results, providing product disposition, ensuring inventory control, performing final inspections, and ensuring compliance with quality procedures and company policies.
What you need
Education
- None
Knowledge / Skills / Abilities
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:
$23.25 - $33.75 Hourly
The 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.
Skills named in this posting
What you'll do
- Apply and remove holds in the system and Q-Tag.
- Assess and repackage inbound damaged goods.
- Communicate with divisional partners to determine product disposition.
- Maintain communication with branch personnel and divisional partners.
- Operate material handling equipment (e.g., reach truck, order picker) to manage inventory.
- Assist with item adjustments and other inventory-related tasks.
- Prioritize and perform recall activities, including stock checks, deviations, relabels, product rework, and pedigree verification.
- Coordinate project/rework areas and resources.
- Maintain daily reports of held stock using SAP, Excel, and other systems.
- Ensure compliance with SOPs and regulations; communicate with management to address non-conformances.
- Maintain hazardous waste logs and perform weekly audits.
- Use computer systems for communication, reporting, and tracking project time.
- Recommend methods to increase efficiency.
- Ensure shipments are from licensed vendors and maintain electronic logs.
- Perform in-process and final inspections; complete inspection documentation.
- Operate test equipment and perform measurements.
- Identify defects and initiate non-conforming material reports.
- Communicate effectively with quality assurance and production groups.
- Verify and approve line start-up and equipment requirements.
- Participate in continual improvement and customer satisfaction efforts.
- Read and interpret engineering instructions and other documents.
- Comply with quality systems, GMP, GDP, OSHA, and company regulations.
- Review manufacturing/production documents to ensure accuracy.
- Perform line clearance procedures for product release.
- Review and approve Engineering Change Notices (ECNs) and substitutions.
Pay and benefits
$48,360 – $70,200 a year
Employer provided$23.25 – $33.75 an hour · yearly at 2,080 hours (40 a week)
How this comparesHealth insurance
Life and disability insurance
401(k) contributions
Paid time off
Continuing education and training
Employee Assistance Program
Where you'll work
Neptune, NJOn-siteOpen in Maps (opens in a new tab)
More jobs in Neptune, NJEqual opportunity, accessibility and legal noticesMedline's statements, word for word
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.
Job intelligence
The context around this role
Live data · November 8, 2026
Salary intelligence
How the pay compares
This role's midpoint is 24% above the US median for Quality Inspection roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US54 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $48,360 | — | $70,200 |
| All US (middle half) | $46,250 | $48,000 | $51,875 |
This role: Medline's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Inspection roles at the same level on Regulatory Jobs, November 8, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Inspection
The general path across 100 open Quality Inspection roles on Regulatory Jobs, with the titles they carry most. Not Medline's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 33 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs8
- Collaboration and leadership6
- GMP and compliance5
- Investigations and CAPA4
- Lab testing and methods3
- Data and digital systems2
- Quality systems and risk1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Inspection work in medical devices, led by the one this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485Named in the posting
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- FDA21 CFR Part 806(official source, opens in a new tab)Reports of medical device corrections and removals
- FDA21 CFR Part 7(official source, opens in a new tab)FDA enforcement policy, including product recalls
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ISOISO 10993-1(official source, opens in a new tab)Biological evaluation of medical devices within a risk management process
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on medical devices
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- FDA21 CFR Part 830 (UDI)(official source, opens in a new tab)Unique device identification and the GUDID database
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDA21 CFR Part 801(official source, opens in a new tab)FDA labeling requirements for medical devices
Company hiring pulse
Medline on Regulatory Jobs
- 56
- Open roles
- 56
- Distinct roles
- 20
- Locations
By discipline
- Quality52 85%
- Regulatory8 13%
- Clinical1 2%
By level
- Associate & Specialist41 67%
- Senior & Principal14 23%
- Manager3 5%
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Quality Control Inspector II (1st Shift) at Medline
Open until filled. $48K–$70K a year, employer provided.