Medical Device QC Inspector Your responsibilities Position Summary: The QC Inspector will be ... Will operate in accordance with company procedures, FDA Regulations, ISO 13485 and Canadian Medical ...
Medical Device QC Inspector Your responsibilities Position Summary: The QC Inspector will be ... Will operate in accordance with company procedures, FDA Regulations, ISO 13485 and Canadian Medical ...
FDA Compliance Specialist
Horsham, PA · On-site
$10K/mo
Represent Airgas during on-site inspections by the FDA, other government agencies, and customers. * Maintain specialized guidance regarding current and developing food, drug, and standards and ...
FDA Compliance Specialist
Horsham, PA · On-site
$10K/mo
Represent Airgas during on-site inspections by the FDA, other government agencies, and customers. * Maintain specialized guidance regarding current and developing food, drug, and standards and ...
The Senior Quality Inspector will be responsible for performing inspection on medical devices to ... Will operate in accordance with company procedures, FDA Regulations, ISO 13485 and Canadian Medical ...
The Senior Quality Inspector will be responsible for performing inspection on medical devices to ... Will operate in accordance with company procedures, FDA Regulations, ISO 13485 and Canadian Medical ...
Participate in Mock inspections for FDA inspection preparation Qualifications Ability to work independently with little or no supervision Exeptional oral and written communication capabilities ...
Participate in Mock inspections for FDA inspection preparation Qualifications Ability to work independently with little or no supervision Exeptional oral and written communication capabilities ...
Participate in Mock inspections for FDA inspection preparation Qualifications Ability to work independently with little or no supervision Exeptional oral and written communication capabilities ...
Participate in Mock inspections for FDA inspection preparation Qualifications Ability to work independently with little or no supervision Exeptional oral and written communication capabilities ...
Ensure compliance with FDA, ISO 13485, GMP, and company requirements. Qualifications Required: * High school diploma or equivalent. * 1-3 years of QC inspection experience in a manufacturing ...
Ensure compliance with FDA, ISO 13485, GMP, and company requirements. Qualifications Required: * High school diploma or equivalent. * 1-3 years of QC inspection experience in a manufacturing ...
Ensure compliance with FDA, ISO 13485, GMP, and company requirements. Qualifications Required: * High school diploma or equivalent. * 1-3 years of QC inspection experience in a manufacturing ...
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Ensure compliance with FDA, ISO 13485, GMP, and company requirements. Qualifications Required: * High school diploma or equivalent. * 1-3 years of QC inspection experience in a manufacturing ...
This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining ...
This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining ...
This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining ...
This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining ...
This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining ...
This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining ...
This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining ...
This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining ...
Be Seen First
QA Inspector (7:00am - 3:30pm; Pharma Experience Required)
Newtown, PA · On-site
$23 - $27/hr
QA Inspector About KVK Tech KVK Tech is a U.S.-based generic and specialty pharmaceutical ... quality, FDA-approved medicines that improve patients' lives through accessibility and trust.
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Be Seen First
QA Inspector (7:00am - 3:30pm; Pharma Experience Required)
Newtown, PA · On-site
$23 - $27/hr
QA Inspector About KVK Tech KVK Tech is a U.S.-based generic and specialty pharmaceutical ... quality, FDA-approved medicines that improve patients' lives through accessibility and trust.
Previous medical device manufacturing experience and a working knowledge of FDA QSR and ISO 13485 ... inspection tools. * Must be familiar with engineering drawings. * Strong working knowledge of ...
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Previous medical device manufacturing experience and a working knowledge of FDA QSR and ISO 13485 ... inspection tools. * Must be familiar with engineering drawings. * Strong working knowledge of ...
Quality Inspector II
Bethlehem, PA · On-site
Previous medical device manufacturing experience and a working knowledge of FDA QSR and ISO 13485 ... inspection tools. * Must be familiar with engineering drawings. * Strong working knowledge of ...
Quick apply
Quality Inspector II
Bethlehem, PA · On-site
Previous medical device manufacturing experience and a working knowledge of FDA QSR and ISO 13485 ... inspection tools. * Must be familiar with engineering drawings. * Strong working knowledge of ...
Senior Quality Inspector - CMM & Metrology
Hatboro, PA · On-site
$26 - $32/hr
Document inspection results clearly and accurately according to Good Documentation Practices , ISO 13485, AS9100, FDA, and internal quality system requirements. * Support nonconformance reporting ...
Senior Quality Inspector - CMM & Metrology
Hatboro, PA · On-site
$26 - $32/hr
Document inspection results clearly and accurately according to Good Documentation Practices , ISO 13485, AS9100, FDA, and internal quality system requirements. * Support nonconformance reporting ...
Lead and represent the sites during FDA inspections, Notified Body audits, customer audits, and regulatory authority interactions, maintaining a continuous state of inspection readiness. * Drive ...
Lead and represent the sites during FDA inspections, Notified Body audits, customer audits, and regulatory authority interactions, maintaining a continuous state of inspection readiness. * Drive ...
Quality Manager
Mount Bethel, PA · On-site
$85K - $95K/yr
... FDA inspections and customer audits. · Collaborate with R&D, production, and regulatory teams to ensure quality is built into all stages of product development and manufacturing. · Direct ...
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Quality Manager
Mount Bethel, PA · On-site
$85K - $95K/yr
... FDA inspections and customer audits. · Collaborate with R&D, production, and regulatory teams to ensure quality is built into all stages of product development and manufacturing. · Direct ...
Lead and represent the sites during FDA inspections, Notified Body audits, customer audits, and regulatory authority interactions, maintaining a continuous state of inspection readiness. * Drive ...
Lead and represent the sites during FDA inspections, Notified Body audits, customer audits, and regulatory authority interactions, maintaining a continuous state of inspection readiness. * Drive ...
C&J Industries is a full service plastic injection molding contract manufacturer and FDA certified ... Key Responsibilities: - Conduct inspections of plastic products throughout various stages of ...
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C&J Industries is a full service plastic injection molding contract manufacturer and FDA certified ... Key Responsibilities: - Conduct inspections of plastic products throughout various stages of ...
The Quality Control Inspector is responsible for performing inspections at various stages of ... Administration (FDA), Quality System Regulations (QSRs), International Organization of ...
The Quality Control Inspector is responsible for performing inspections at various stages of ... Administration (FDA), Quality System Regulations (QSRs), International Organization of ...
Fda Inspector information
See Pennsylvania salary details
$24.6K - $31.3K
3% of jobs
$31.3K - $38.1K
16% of jobs
$39.8K is the 25th percentile. Wages below this are outliers.
$38.1K - $44.9K
23% of jobs
The median wage is $47K / yr.
$44.9K - $51.7K
27% of jobs
$56.1K is the 75th percentile. Wages above this are outliers.
$51.7K - $58.5K
10% of jobs
$58.5K - $65.3K
4% of jobs
$65.3K - $72.1K
5% of jobs
$72.1K - $78.9K
2% of jobs
$78.9K - $85.7K
2% of jobs
$85.7K - $92.4K
2% of jobs
$92.4K - $99.2K
5% of jobs
$24.6K
$55.1K
$99.2K
How much do fda inspector jobs pay per year?
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?
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The most popular types of Fda Inspector jobs in Pennsylvania are:
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For Fda Inspector jobs in Pennsylvania, the most frequently searched job titles are:
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Job description
Medical Device QC Inspector
Your responsibilities
Position Summary:
The QC Inspector will be responsible for performing inspection on medical devices to specified requirements to determine product disposition. Will operate in accordance with company procedures, FDA Regulations, ISO 13485 and Canadian Medical Device Regulations, and other applicable requirements.
Responsibilities: Essential Duties
Perform mechanical, visual, packaging and document Inspection of orthopedic medical devices
Complete all required documentation of the inspection results, on handwritten forms, and electronic spreadsheets or databases, in accordance with company procedures and work instructions.
Identify and document potentially non-conforming product.
Ensure non-conforming product is properly segregated and quarantined.
Interface with other departments, to address and resolve any product related issues.
Assist with labeling of product and label reconciliation.
Perform line clearance to ensure that product integrity is maintained.
Read, understand, and follow company procedures and policies.
Skills and Qualifications:
Educational Requirements: High school diploma/GED (Required)
o Associate's Degree (Desired)
Working knowledge of use of various gauges such as calipers, micrometers, thread gauges, etc.
Knowledge of quality practices, FDA Regulations and ISO 13485.
Knowledgeable of inspection techniques.
Basic understand of reading engineering drawings.
Good verbal and written communication skills.
Strong attention to detail and accurate record keeping.
Basic computer skills including a word processing, and spreadsheet, etc.
Must be flexible and able to adapt to changes in priorities.
Must be able to occasionally lift up to 25 lbs.
About Tyber Medical
Sourced by ZipRecruiter
Industry
Medical equipment and supplies manufacturing
Company size
51 - 200 Employees
Headquarters location
Bethlehem, PA, US
Year founded
2012