New · posted Nov 5
Medline · Medical Devices
Manufacturing Quality Control Supervisor - 2nd shift
- Hartland, WI
- On-site
- Part-time
- Manager
The role
Oversee and manage the Quality Control functions and personnel at designated distribution center. Responsibilities Include inspection, product disposition, holding and releasing of product and personnel matters.
What you need
Education
- High school diploma or equivalent.
Education
- Associates degree or technical certification preferred.
Certification / Licensure
- None
Work Experience
- At least 3 years QC or similar experience.
- Prior experience in medical device and/or drug manufacturing setting.
Knowledge / Skills / Abilities
- Intermediate level understanding of FDA/ QSR/ ISO-13485 guidelines.
- Intermediate level knowledge of ANSI/ ASQCZ1.4-current revision.
- Intermediate level skill in Microsoft Excel (for example: using SUM function, setting borders, setting column width, inserting charts, using text wrap, sorting, setting headers and footers and/or print scaling).
- Intermediate level skill in Microsoft Word (for example: inserting headers, page breaks, page numbers and tables and/or adjusting table columns).
- Ability to lift up to 50 pounds. Sit, walk or stand for prolong periods of time. Display specific vision abilities including, close vision, distance vision, depth perception and ability to adjust focus. Ability to work in hot and cold environments, (32F – 95F). Ability to encompass heights. Frequent
- Must be available to travel from state to state on occasion.
Work Experience
- Supervising or managing experience preferred.
Knowledge / Skills / Abilities
- Operating Material Handling Equipment.
- Knowledge of Quality Systems Regulations and Medical Devices preferred.
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:
$79,000.00 - $119,000.00 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 page here.
What you'll do
- Manage all performance, attendance, monthly bonus and employee reviews for direct reports at designated distribution center.
- Prioritize work schedules. Schedule overtime as needed.
- Maintain a good working relationship and open communications with Branch Management.
- Train branch inspectors on Quality System Regulation (QSR), Department of Health/ Board of Pharmacy rules and regulations.
- Support Quality, Regulalatory and Operations to ensure branch compliance with all applicable regualtions.
- Lead day-to-day activities of employees. Assign, monitor and review progress and accuracy of work, directs efforts and provides technical guidance on more complex issues. Provide input into hiring, firing and performance reviews.
- Operate material handling equipment as necessary to support workload and overall projects.
Pay and benefits
$79,000 – $119,000 a year
Employer provided401(k) contributions
Paid time off
Employee Assistance Program
Employee Resource Groups
Health insurance (30+ hours/week)
Life and disability insurance (30+ hours/week)
Where you'll work
Hartland, WIOn-siteOpen in Maps (opens in a new tab)
More jobs in Hartland, WIEqual 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 5, 2026
Salary intelligence
How the pay compares
This role's midpoint is 26% below the US median for Quality Operations & Batch Release roles at this level.
This roleEmployer provided
Manager roles in the US14 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $79,000 | — | $119,000 |
| All US (middle half) | $119,125 | $133,250 | $152,500 |
This role: Medline's own published range. Comparisons: the base pay employers published on open Quality Operations & Batch Release roles at the same level on Regulatory Jobs, November 5, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Operations & Batch Release
The general path across 87 open Quality Operations & Batch Release 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 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance4
- Collaboration and leadership4
- Quality systems and risk3
- Documentation and SOPs1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Operations & Batch Release work in medical devices, led by the three 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 13485(official source, opens in a new tab)Quality management systems for medical devicesNamed in the posting
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)Named in the posting
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- FDA21 CFR Part 806(official source, opens in a new tab)Reports of medical device corrections and removals
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
- FDAMDSAP(official source, opens in a new tab)The Medical Device Single Audit Program shared by five regulators
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDA21 CFR Part 830 (UDI)(official source, opens in a new tab)Unique device identification and the GUDID database
- FDAFDA Computer Software Assurance(official source, opens in a new tab)Risk-based assurance for production and quality system software
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- FDA21 CFR Part 807(official source, opens in a new tab)Establishment registration, device listing and premarket notification
- IECIEC 62366-1(official source, opens in a new tab)Application of usability engineering to medical devices
- Health CanadaCanada Medical Devices Regulations(official source, opens in a new tab)Health Canada's licensing and quality requirements for medical devices (SOR/98-282)
Company hiring pulse
Medline on Regulatory Jobs
- 61
- Open roles
- 45
- Distinct roles
- 19
- Locations
By discipline
- Quality52 85%
- Regulatory8 13%
- Clinical1 2%
By level
- Associate & Specialist40 66%
- Senior & Principal15 25%
- Manager3 5%
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Manufacturing Quality Control Supervisor - 2nd shift at Medline
Open until filled. $79K–$119K a year, employer provided.