

New · posted Nov 12
Pride Mobility Products · Medical Devices
Quality Inspector
- Pontotoc, MS
- On-site
- Full-time
- Associate & Specialist
The role
DESCRIPTION/JOB SUMMARY
Perform final visual and physical inspections on finished goods to meet order specifications, production standards and Food and Drug Administration (FDA) regulations
DETAILS
•This is a safety sensitive position
What you need
REQUIRED SKILLS
•Must be a friendly team player, detail-oriented, and honest
Must have the ability to:
•Multi-task, problem-solve, and prioritize in a fast-paced working environment
•Read and interpret work instructions, work orders, inspection criteria, tape measures, policies, and procedures
•Identify and record facts
•Stand/Walk/Bend throughout the workday
•Lift/Push/Pull 40 lbs.
Must have:
•Relentless drive to achieve advancement and continuous improvement
•A willingness to learn and/or adapt to new work methods
•Basic computer skills
•Good verbal and written communication skills
REQUIRED EXPERIENCE
•At least 6 months of Quality Assurance experience OR at least 2 years of experience in a hands-on assembly or manufacturing role with specific quality guidelines/standards
PREFERRED EDUCATIONnice to have
•High School Diploma or GED preferred
•American Society for Quality (ASQ) certification preferred
REQUIRED QUALIFICATIONS
•Must be legally authorized to work in the United States without sponsorship now, or in the future
PREFERRED SKILLSnice to have
•Basic working knowledge of Microsoft Office Word and Excel preferred
PREFERRED EXPERIENCEnice to have
•Current or previous successful employment experience with Pride Mobility Products Corporation preferred
What you'll do
RESPONSIBILITIES/DUTIES
•Inspect finished product for defects or imperfections in aesthetics and function and to ensure tolerances and product specifications are met
•Ensure conformance to order specifications and FDA regulations
•Utilize the ProductionWare (Matrix) system and ensure that all pertinent product information is documented and recorded onto the Device History Record (DHR)
•Use a team-oriented approach and communicate concerns and issues to management
•Follow Work Instructions and perform duties assigned with minimal supervision
•Ensure all safety and security rules are strictly observed and any accidents, incidents or injuries are promptly reported to management
•Complete the annual CTPAT Security Training
•Focus on continuous improvement, and consistently demonstrate good business judgment
•Work effectively with all Pride departments to exceed internal and external expectations
•Assist with organization and cleaning of work area, keeping aisles and walkways clear at all times
•Pride retains the discretion to modify duties and/or assign other duties as necessary
Pay
Where you'll work
Pontotoc, MSOn-siteOpen in Maps (opens in a new tab)
More jobs in Pontotoc, MSEqual opportunity, accessibility and legal noticesPride Mobility Products's statements, word for word
•This job description is not intended to be all-inclusive
•In exceptional circumstances, some of the physical requirements of this position may be modified or eliminated as a reasonable accommodation for a person with a disability as defined by the Americans with Disabilities Act
Pride Mobility Products®/Quantum Rehab® is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, physical or mental disability, protected Veteran status, age, or any other characteristic protected by federal, state, or local law. Pride Mobility Products®/Quantum Rehab® is an Affirmative Action Employer with obligations under VEVRAA and Section 503 of the Rehabilitation Act of 1973 for protected veterans and individuals with disabilities.
If you are a person with a disability, a disabled veteran, or require a reasonable accommodation or assistance in completing an application for employment, please contact our human resources department at 1-800-800-8586 x1250.
Job intelligence
The context around this role
Live data · November 12, 2026
Salary intelligence
How the pay compares
This role's midpoint is 23% below the US median for Quality Inspection roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US58 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $36,920 | — | $36,920 |
| All US (middle half) | $46,000 | $48,000 | $51,500 |
This role: Pride Mobility Products'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 12, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Inspection
The general path across 106 open Quality Inspection roles on Regulatory Jobs, with the titles they carry most. Not Pride Mobility Products's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 31 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership4
- GMP and compliance3
- Documentation and SOPs3
- Quality systems and risk2
- Data and digital systems2
- Lab testing and methods1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Inspection work in medical devices, 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 13485
- 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
- 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 806(official source, opens in a new tab)Reports of medical device corrections and removals
- 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
- ISOISO 15223-1(official source, opens in a new tab)Symbols for medical device labels and labeling
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
Company hiring pulse
Pride Mobility Products on Regulatory Jobs
- 5
- Open roles
- 5
- Distinct roles
- 4
- Locations
By discipline
- Quality5 100%
By level
- Associate & Specialist4 80%
- Senior & Principal1 20%
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Quality Inspector at Pride Mobility Products
Open until filled. $37K a year, employer provided.


