Experience overseeing incoming, in-process, and finished goods inspection and testing activities. * Strong knowledge of FDA Quality System Regulation, ISO 13485, and Good Manufacturing Practices (GMP ...
Experience overseeing incoming, in-process, and finished goods inspection and testing activities. * Strong knowledge of FDA Quality System Regulation, ISO 13485, and Good Manufacturing Practices (GMP ...
Inspect work during the build process and perform basic functional checks to ensure quality * Accurately document production work in accordance with GMP and ISO/FDA requirements * Identify defects or ...
Inspect work during the build process and perform basic functional checks to ensure quality * Accurately document production work in accordance with GMP and ISO/FDA requirements * Identify defects or ...
Ensures site audit readiness and hosting Quality System audits and inspections * Supports the ... Hands-on experience with FDA, QSR, ISO, MDD and/or other international quality systems requirements ...
Ensures site audit readiness and hosting Quality System audits and inspections * Supports the ... Hands-on experience with FDA, QSR, ISO, MDD and/or other international quality systems requirements ...
Director of Food Safety
Lehi, UT · On-site
Maintain compliance with the FDA Food Code and all applicable state, county, and municipal ... for inspections, plan reviews, and variances. * Own the ServSafe Manager certification program ...
Director of Food Safety
Lehi, UT · On-site
Maintain compliance with the FDA Food Code and all applicable state, county, and municipal ... for inspections, plan reviews, and variances. * Own the ServSafe Manager certification program ...
QC Microbiologist
South Ogden, UT · On-site
$55 - $75/hr
Inspect/audit lab activities and data to ensure implementation of quality systems * Provide back ... In depth knowledge of USP, AOAC, FDA BAM microbiological testing methods * Knowledge of allergen ...
QC Microbiologist
South Ogden, UT · On-site
$55 - $75/hr
Inspect/audit lab activities and data to ensure implementation of quality systems * Provide back ... In depth knowledge of USP, AOAC, FDA BAM microbiological testing methods * Knowledge of allergen ...
Ensures site audit readiness and hosting Quality System audits and inspections * Supports the ... Hands-on experience with FDA, QSR, ISO, MDD and/or other international quality systems requirements ...
Ensures site audit readiness and hosting Quality System audits and inspections * Supports the ... Hands-on experience with FDA, QSR, ISO, MDD and/or other international quality systems requirements ...
... inspections, assist with site planning and interaction with customers and contractors as needed to insure preparation of the site to OEM specifications. * Completion of all necessary state and FDA ...
... inspections, assist with site planning and interaction with customers and contractors as needed to insure preparation of the site to OEM specifications. * Completion of all necessary state and FDA ...
Director of Food Safety
Lehi, UT · On-site
Maintain compliance with the FDA Food Code and all applicable state, county, and municipal ... point of contact for inspections, plan reviews, and variances. * Own theServSafeManager ...
Director of Food Safety
Lehi, UT · On-site
Maintain compliance with the FDA Food Code and all applicable state, county, and municipal ... point of contact for inspections, plan reviews, and variances. * Own theServSafeManager ...
Manufacturing Production Supervisor
Lindon, UT · On-site
$55 - $85/hr
Ensure adherence to Good Manufacturing Practices (cGMP), FDA, SQF, HACCP, and company sanitation and safety standards. * Conduct in-process checks, pre-op inspections, and collaborate with Quality ...
Manufacturing Production Supervisor
Lindon, UT · On-site
$55 - $85/hr
Ensure adherence to Good Manufacturing Practices (cGMP), FDA, SQF, HACCP, and company sanitation and safety standards. * Conduct in-process checks, pre-op inspections, and collaborate with Quality ...
Ensure adherence to Good Manufacturing Practices (cGMP), FDA, SQF, HACCP, and company sanitation and safety standards. * Conduct in-process checks, pre-op inspections, and collaborate with Quality ...
Quick apply
Ensure adherence to Good Manufacturing Practices (cGMP), FDA, SQF, HACCP, and company sanitation and safety standards. * Conduct in-process checks, pre-op inspections, and collaborate with Quality ...
Line Lead
$16 - $20.50/hr
Conduct visual inspections of finished goods to verify packaging, labeling, and lot coding meet GMP and company standards. Ensure compliance with GMP, FDA, and facility safety regulations throughout ...
Line Lead
$16 - $20.50/hr
Conduct visual inspections of finished goods to verify packaging, labeling, and lot coding meet GMP and company standards. Ensure compliance with GMP, FDA, and facility safety regulations throughout ...
Ensure adherence to Good Manufacturing Practices (cGMP), FDA, SQF, HACCP, and company sanitation and safety standards. * Conduct in-process checks, pre-op inspections, and collaborate with Quality ...
Ensure adherence to Good Manufacturing Practices (cGMP), FDA, SQF, HACCP, and company sanitation and safety standards. * Conduct in-process checks, pre-op inspections, and collaborate with Quality ...
Ensure adherence to Good Manufacturing Practices (cGMP), FDA, SQF, HACCP, and company sanitation and safety standards. * Conduct in-process checks, pre-op inspections, and collaborate with Quality ...
Ensure adherence to Good Manufacturing Practices (cGMP), FDA, SQF, HACCP, and company sanitation and safety standards. * Conduct in-process checks, pre-op inspections, and collaborate with Quality ...
Inventory Specialist I
West Valley City, UT · On-site
$60K - $80K/yr
Prepare and support regulatory inspections by the FDA, EMA, and other health authorities. * Create, review, and revise related documents, including SOPs and forms. * Participate in quality systems ...
Inventory Specialist I
West Valley City, UT · On-site
$60K - $80K/yr
Prepare and support regulatory inspections by the FDA, EMA, and other health authorities. * Create, review, and revise related documents, including SOPs and forms. * Participate in quality systems ...
Inventory Specialist I
$60K - $80K/yr
Prepare and support regulatory inspections by the FDA, EMA, and other health authorities. * Create, review, and revise related documents, including SOPs and forms. * Participate in quality systems ...
Inventory Specialist I
$60K - $80K/yr
Prepare and support regulatory inspections by the FDA, EMA, and other health authorities. * Create, review, and revise related documents, including SOPs and forms. * Participate in quality systems ...
Inventory Specialist I
West Valley City, UT · On-site
$60 - $80/hr
Prepare and support regulatory inspections by the FDA, EMA, and other health authorities. * Create, review, and revise related documents, including SOPs and forms. * Participate in quality systems ...
Inventory Specialist I
West Valley City, UT · On-site
$60 - $80/hr
Prepare and support regulatory inspections by the FDA, EMA, and other health authorities. * Create, review, and revise related documents, including SOPs and forms. * Participate in quality systems ...
CAPA Process Lead
Salt Lake City, UT · On-site
Experience supporting FDA, notified body, MDSAP, or other regulatory inspections and audits. Time Type: Full time Job Type: Regular Work Shift: First Shift Pay Rate Type: Salary Benefits and Perks ...
CAPA Process Lead
Salt Lake City, UT · On-site
Experience supporting FDA, notified body, MDSAP, or other regulatory inspections and audits. Time Type: Full time Job Type: Regular Work Shift: First Shift Pay Rate Type: Salary Benefits and Perks ...
CAPA Process Lead
Salt Lake City, UT · On-site
Experience supporting FDA, notified body, MDSAP, or other regulatory inspections and audits. Time Type: Full time Job Type: Regular Work Shift: First Shift Pay Rate Type: Salary Benefits and Perks ...
CAPA Process Lead
Salt Lake City, UT · On-site
Experience supporting FDA, notified body, MDSAP, or other regulatory inspections and audits. Time Type: Full time Job Type: Regular Work Shift: First Shift Pay Rate Type: Salary Benefits and Perks ...
QA Supervisor- Food
Salt Lake City, UT · On-site
$55K/yr
... requirements (FDA, USDA, etc.), and customer specifications. This role supervises the QA team, supports plant inspections, and helps drive continuous quality improvement initiatives. Job type
QA Supervisor- Food
Salt Lake City, UT · On-site
$55K/yr
... requirements (FDA, USDA, etc.), and customer specifications. This role supervises the QA team, supports plant inspections, and helps drive continuous quality improvement initiatives. Job type
Collaborate with cross-functional groups to manage inspection of in-process and finished goods ... Proven ability to serve as a quality representative during internal, notified body, FDA, customer ...
Collaborate with cross-functional groups to manage inspection of in-process and finished goods ... Proven ability to serve as a quality representative during internal, notified body, FDA, customer ...
Fda Inspector information
See Utah salary details
$22.3K - $28.5K
3% of jobs
$28.5K - $34.6K
16% of jobs
$36.2K is the 25th percentile. Wages below this are outliers.
$34.6K - $40.8K
23% of jobs
The median wage is $42.7K / yr.
$40.8K - $47K
27% of jobs
$50.9K is the 75th percentile. Wages above this are outliers.
$47K - $53.1K
10% of jobs
$53.1K - $59.3K
4% of jobs
$59.3K - $65.5K
5% of jobs
$65.5K - $71.6K
2% of jobs
$71.6K - $77.8K
2% of jobs
$77.8K - $84K
2% of jobs
$84K - $90.1K
5% of jobs
$22.3K
$50K
$90.1K
How much do fda inspector jobs pay per year?
As of Sep 5, 2026, the average yearly pay for fda inspector in Utah is $50,015.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,000.00 and $57,800.00 per year, depending on experience, location, and employer.
What does an FDA inspector do?
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.
What skills and qualifications are needed to be an FDA inspector?
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.
What types of facilities or products do FDA inspectors review, and what does a typical inspection process involve?
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.
How do you become an FDA inspector?
To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must pass a written exam and a background check, and often undergo specialized training at the FDA's training center. Certification or licensing is not required but can enhance prospects in the field.
What are popular job titles related to Fda Inspector jobs in Utah?
For Fda Inspector jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Utah look for?
The top searched job categories for Fda Inspector jobs in Utah are:
What cities in Utah are hiring for Fda Inspector jobs?
Cities in Utah with the most Fda Inspector job openings:
Full-time
Posted 24 days ago
Edwards Lifesciences rating
8.2
Based on 31 frontline employees who took The Breakroom Quiz
86th of 545 rated manufacturers
Job description
Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Manager, Manufacturing Quality position is a unique career opportunity that could be your next step towards an exciting future.
The Manager, Manufacturing Quality is responsible for leading Quality Assurance and supporting commercial Metals Manufacturing operations. This role provides leadership and oversight for inspection, testing, nonconformance management, product disposition, quality data review, and compliance activities to ensure product quality, operational excellence, and regulatory compliance. The position partners closely with Manufacturing, Engineering, Supply Chain, and Quality stakeholders to drive timely resolution of quality issues and continuous improvement across commercial production operations.
How You Will Make An Impact:
- Lead Quality Assurance activities and support commercial Metals Manufacturing operations, ensuring compliance with quality system requirements and regulatory standards.
- Direct and develop a team of quality supervisors, inspectors, and quality professionals to support manufacturing operations, product inspection, testing, and release activities.
- Provide leadership and oversight for nonconformance investigations (NCRs), ensuring timely evaluation, containment, disposition, root cause investigation, and closure.
- Establish and maintain quality inspection and testing strategies for in-process and finished products to ensure compliance with product specifications and quality requirements.
- Partner with Manufacturing, Engineering, Supply Chain, and Quality Engineering teams to resolve quality issues, support production objectives, and drive continuous improvement initiatives.
- Oversee product quality disposition activities, including product holds, release decisions, and escalation of quality risks when appropriate.
- Monitor and analyze quality performance metrics and operational trends, providing data-driven recommendations to improve product quality, compliance, and manufacturing performance.
- Ensure inspection processes, testing activities, and quality documentation comply with internal procedures and applicable regulatory requirements.
- Support internal and external audits, regulatory inspections, and management reviews through preparation, execution, and follow-up activities.
- Develop team capabilities through coaching, performance management, succession planning, and technical skill development.
- Identify and implement process improvements to enhance efficiency, effectiveness, and compliance within the Quality Assurance organization.
What You'll Need (Required):
- Bachelor's degree in engineering or scientific disciplines
- Experience within Quality Assurance, Quality Engineering, Manufacturing Quality, or Operations Quality in Medical Device manufacturing; or equivalent experience based on Edwards' criteria.
- Experience directly leading people, including supervisors, inspectors, technicians, and/or professionals.
What Else We Look For (Preferred):
- Engineering or Science degree
- Medical device manufacturing experience.
- Experience leading Quality Assurance teams supporting commercial manufacturing operations.
- Experience with nonconformance management (NCRs), product disposition, initiating and removing product holds, quality investigations, and root cause analysis.
- Experience overseeing incoming, in-process, and finished goods inspection and testing activities.
- Strong knowledge of FDA Quality System Regulation, ISO 13485, and Good Manufacturing Practices (GMP) as they relate to product realization and manufacturing.
- Experience supporting audit readiness, regulatory inspections, and quality management reviews.
- Working knowledge of statistical quality methods, quality metrics, and trend analysis.
- Experience driving continuous improvement initiatives utilizing Lean, Six Sigma, or similar methodologies.
- Experience using quality management systems and enterprise systems such as ETQ, JDE, PLM, SAP, or similar platforms.
- ASQ CQE or other ASQ quality certifications.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
What Edwards Lifesciences employees say
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About Edwards Lifesciences
Sourced by ZipRecruiter
Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.
Industry
Medical equipment and supplies manufacturing
Company size
10,000+ Employees
Headquarters location
Irvine, CA, US
Year founded
1958