Inspector
$20 - $24/hr
FDA inspections knowledge. Additional Skills & Qualifications * Understanding of federal regulations is a plus. * Experience with GMP (training available). * Legible writing skills. * Ability to work ...
New
Quick apply
$20 - $24/hr
FDA inspections knowledge. Additional Skills & Qualifications * Understanding of federal regulations is a plus. * Experience with GMP (training available). * Legible writing skills. * Ability to work ...
New
Quick apply
$20 - $24/hr
FDA inspections knowledge. Additional Skills & Qualifications * Understanding of federal regulations is a plus. * Experience with GMP (training available). * Legible writing skills. * Ability to work ...
New
$20 - $24/hr
FDA inspections knowledge. Additional Skills & Qualifications * Understanding of federal regulations is a plus. * Experience with GMP (training available). * Legible writing skills. * Ability to work ...
New
Quick apply
$20 - $24/hr
FDA inspections knowledge. Additional Skills & Qualifications * Understanding of federal regulations is a plus. * Experience with GMP (training available). * Legible writing skills. * Ability to work ...
New
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations. Usona's team is small, close knit, and deeply ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations. Usona's team is small, close knit, and deeply ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations.Usona's team is small, close knit, and deeply ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations.Usona's team is small, close knit, and deeply ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations. Usona's team is small, close knit, and deeply ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations. Usona's team is small, close knit, and deeply ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations. Usona's team is small, close knit, and deeply ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations. Usona's team is small, close knit, and deeply ...
Madison, WI · On-site
$30/hr
Follow all established procedures in compliance with FDA and ISO 13485:2008 standards. * Maintain documentation in accordance with GMP and company policies. * Adapt to various inspection assignments ...
Quick apply
Madison, WI · On-site
$30/hr
Follow all established procedures in compliance with FDA and ISO 13485:2008 standards. * Maintain documentation in accordance with GMP and company policies. * Adapt to various inspection assignments ...
Madison, WI · On-site
$30/hr
The Medical Device Quality Inspector is responsible for ensuring that all materials, processes, and packaging activities comply with current GMP standards , FDA regulations , and company quality ...
Quick apply
Madison, WI · On-site
$30/hr
The Medical Device Quality Inspector is responsible for ensuring that all materials, processes, and packaging activities comply with current GMP standards , FDA regulations , and company quality ...
Madison, WI · On-site
$30/hr
Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $30/hr (W2) Job Summary ... Familiarity with FDA Quality System Regulations and ISO 13485 standards for medical device ...
Quick apply
Madison, WI · On-site
$30/hr
Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $30/hr (W2) Job Summary ... Familiarity with FDA Quality System Regulations and ISO 13485 standards for medical device ...
Madison, WI · On-site
... of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing ... inspector
Madison, WI · On-site
... of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing ... inspector
$60K - $63K/hr
Audit and Inspection Support * Provide requested documentation during FDA inspections, SQF audits, customer audits, and third-party assessments. * Ensure audit-ready documentation is readily ...
$60K - $63K/hr
Audit and Inspection Support * Provide requested documentation during FDA inspections, SQF audits, customer audits, and third-party assessments. * Ensure audit-ready documentation is readily ...
Sturtevant, WI · On-site
$19.35 - $25.09/hr
Indicating inspection status maintains product traceability and non-conforming material control ... FDA Quality System Regulations, and other customer requirements. An individual in this position ...
Sturtevant, WI · On-site
$19.35 - $25.09/hr
Indicating inspection status maintains product traceability and non-conforming material control ... FDA Quality System Regulations, and other customer requirements. An individual in this position ...
Sturtevant, WI · On-site
$19.35 - $25.09/hr
Indicating inspection status maintains product traceability and non-conforming material control ... FDA Quality System Regulations, and other customer requirements. An individual in this position ...
Sturtevant, WI · On-site
$19.35 - $25.09/hr
Indicating inspection status maintains product traceability and non-conforming material control ... FDA Quality System Regulations, and other customer requirements. An individual in this position ...
$19.35 - $25.09/hr
Indicating inspection status maintains product traceability and non-conforming material control ... FDA Quality System Regulations, and other customer requirements. An individual in this position ...
$19.35 - $25.09/hr
Indicating inspection status maintains product traceability and non-conforming material control ... FDA Quality System Regulations, and other customer requirements. An individual in this position ...
Conduct inspections and case audits to verify adherence to GMP, SQF, HACCP, FDA, and state regulations, as well as internal quality policies and procedures. * Review and verify Certificates of ...
New
Quick apply
Conduct inspections and case audits to verify adherence to GMP, SQF, HACCP, FDA, and state regulations, as well as internal quality policies and procedures. * Review and verify Certificates of ...
New
Be Seen First
Milwaukee, WI · On-site
$24 - $26/hr
This role supports senior quality staff with final inspections, product release documentation, and compliance with ISO and FDA quality standards. Key Responsibilities * Inspect incoming materials and ...
Quick apply
Be Seen First
Milwaukee, WI · On-site
$24 - $26/hr
This role supports senior quality staff with final inspections, product release documentation, and compliance with ISO and FDA quality standards. Key Responsibilities * Inspect incoming materials and ...
Milwaukee, WI · On-site
$24 - $26/hr
This role supports senior quality staff with final inspections, product release documentation, and compliance with ISO and FDA quality standards. Key Responsibilities * Inspect incoming materials and ...
Quick apply
Milwaukee, WI · On-site
$24 - $26/hr
This role supports senior quality staff with final inspections, product release documentation, and compliance with ISO and FDA quality standards. Key Responsibilities * Inspect incoming materials and ...
$150K - $198K/yr
Ensure inspection readiness for FDA and notified body audits. * Conduct ongoing company-wide training on FDA and ISO requirements * Oversee: * CAPA systems * Complaint handling and vigilance ...
$150K - $198K/yr
Ensure inspection readiness for FDA and notified body audits. * Conduct ongoing company-wide training on FDA and ISO requirements * Oversee: * CAPA systems * Complaint handling and vigilance ...
Middleton, WI · On-site
$150K - $198K/yr
Ensure inspection readiness for FDA and notified body audits. * Conduct ongoing company-wide training on FDA and ISO requirements * Oversee: * CAPA systems * Complaint handling and vigilance ...
Middleton, WI · On-site
$150K - $198K/yr
Ensure inspection readiness for FDA and notified body audits. * Conduct ongoing company-wide training on FDA and ISO requirements * Oversee: * CAPA systems * Complaint handling and vigilance ...
Kenosha, WI · On-site
$20 - $25/hr
Enter inspection data into ERP systems, spreadsheets, and quality databases * Ensure all records and documentation comply with ISO 13485, FDA, and company quality requirements * Meet established ...
Quick apply
Kenosha, WI · On-site
$20 - $25/hr
Enter inspection data into ERP systems, spreadsheets, and quality databases * Ensure all records and documentation comply with ISO 13485, FDA, and company quality requirements * Meet established ...
$24.7K - $31.6K
3% of jobs
$31.6K - $38.4K
16% of jobs
$40.1K is the 25th percentile. Wages below this are outliers.
$38.4K - $45.2K
23% of jobs
The median wage is $47.3K / yr.
$45.2K - $52.1K
27% of jobs
$56.4K is the 75th percentile. Wages above this are outliers.
$52.1K - $58.9K
10% of jobs
$58.9K - $65.7K
4% of jobs
$65.7K - $72.6K
5% of jobs
$72.6K - $79.4K
2% of jobs
$79.4K - $86.3K
2% of jobs
$86.3K - $93.1K
2% of jobs
$93.1K - $99.9K
5% of jobs
$24.7K
$55.5K
$99.9K
FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.
To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.
An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.

$20 - $24/hr
Contractor
Medical, Dental, Vision, Life, Retirement, PTO
Posted yesterday
As an Inspector, you will oversee all incoming component inspections, conduct in-line and in-process checks, issue labels, and manage any special projects that require inspection. You will also handle AQL inspections in response to customer complaints and participate in rework activities. The role involves managing over 1200 samples for a production lot, performing quality checks of medical products throughout the manufacturing and packaging process, and ensuring compliance with quality standards.
ResponsibilitiesThe work environment includes a growing company with a supportive culture that encourages internal growth. The shift options are QC #1: 3:00PM to 11:30PM (Monday – Friday), QC #2: 6:00PM – close (Monday – Friday), QC #3: 1:30PM – 10:00PM (Monday – Friday), QC #4: 6:00AM – 4:30PM (Friday – Monday), and QC #5: 6:00PM – 4:30AM (Friday – Monday). The company manufactures OTC drugs, cosmetics, and medical devices, primarily producing lubricating jellies, shampoos, and saline syringes. The role is split evenly between floor inspections/auditing and office documentation work. Benefits include paid holidays and prorated vacation time, contributing to an attractive work-life balance.
Job Type & LocationThis is a Contract to Hire position based out of Milwaukee, WI.
Pay and BenefitsThe pay range for this position is $20.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace TypeThis is a fully onsite position in Milwaukee,WI.
Application DeadlineThis position is anticipated to close on Aug 7, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
Sourced by ZipRecruiter
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
5,001 - 10,000 Employees
Hanover, MD, US
1983