Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Quick apply
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Manager, QC Microbiology (Sterile Drug Manufacturing & Fill Finish)
Danbury, CT · On-site
$116K - $174K/yr
Experience supporting regulatory inspections (FDA, EMA, MHRA). * Understanding of water system microbiology and clean utility qualification. * Lean/Six Sigma or continuous improvement training. Pay ...
Manager, QC Microbiology (Sterile Drug Manufacturing & Fill Finish)
Danbury, CT · On-site
$116K - $174K/yr
Experience supporting regulatory inspections (FDA, EMA, MHRA). * Understanding of water system microbiology and clean utility qualification. * Lean/Six Sigma or continuous improvement training. Pay ...
... and agency inspections and/or audits as necessary. They also assess and advise on regulatory ... US FDA 510(k) submissions. * US FDA Pre-submissions (Q-subs). * EU MDR Submissions. * UK ...
... and agency inspections and/or audits as necessary. They also assess and advise on regulatory ... US FDA 510(k) submissions. * US FDA Pre-submissions (Q-subs). * EU MDR Submissions. * UK ...
... and agency inspections and/or audits as necessary. They also assess and advise on regulatory ... US FDA 510(k) submissions. * US FDA Pre-submissions (Q-subs). * EU MDR Submissions. * UK ...
... and agency inspections and/or audits as necessary. They also assess and advise on regulatory ... US FDA 510(k) submissions. * US FDA Pre-submissions (Q-subs). * EU MDR Submissions. * UK ...
... and agency inspections and/or audits as necessary. They also assess and advise on regulatory ... US FDA 510(k) submissions. * US FDA Pre-submissions (Q-subs). * EU MDR Submissions. * UK ...
Quick apply
... and agency inspections and/or audits as necessary. They also assess and advise on regulatory ... US FDA 510(k) submissions. * US FDA Pre-submissions (Q-subs). * EU MDR Submissions. * UK ...
Manager, QA Validation (Sterile Manufacturing)
Danbury, CT · On-site
$116K - $174K/yr
Experience supporting regulatory inspections (FDA, EMA, MHRA). Lean/Six Sigma or continuous improvement training. Pay Range: $116,000 - $174,000 per year
Manager, QA Validation (Sterile Manufacturing)
Danbury, CT · On-site
$116K - $174K/yr
Experience supporting regulatory inspections (FDA, EMA, MHRA). Lean/Six Sigma or continuous improvement training. Pay Range: $116,000 - $174,000 per year
Manager, QA Validation (Sterile Manufacturing)
Danbury, CT · On-site
$116K - $174K/yr
Experience supporting regulatory inspections (FDA, EMA, MHRA). Lean/Six Sigma or continuous improvement training.
Manager, QA Validation (Sterile Manufacturing)
Danbury, CT · On-site
$116K - $174K/yr
Experience supporting regulatory inspections (FDA, EMA, MHRA). Lean/Six Sigma or continuous improvement training.
Supervisor Quality Control
Dayville, CT · On-site
... FDA and/or CGMP * 5+ years of quality control and/or laboratory experience, preferable in a manufacturing and/or medical organization. * American Society of Quality (ASQ) Certified Quality Inspector ...
Supervisor Quality Control
Dayville, CT · On-site
... FDA and/or CGMP * 5+ years of quality control and/or laboratory experience, preferable in a manufacturing and/or medical organization. * American Society of Quality (ASQ) Certified Quality Inspector ...
This role plays a keypartin driving inspection readiness and supporting continuous improvement ... FDA QMSR / 21 CFR Part 820 transition to ISO 13485 * ISO 13485 Quality Management Systems
This role plays a keypartin driving inspection readiness and supporting continuous improvement ... FDA QMSR / 21 CFR Part 820 transition to ISO 13485 * ISO 13485 Quality Management Systems
This role plays a keypartin driving inspection readiness and supporting continuous improvement ... FDA QMSR / 21 CFR Part 820 transition to ISO 13485 * ISO 13485 Quality Management Systems
This role plays a keypartin driving inspection readiness and supporting continuous improvement ... FDA QMSR / 21 CFR Part 820 transition to ISO 13485 * ISO 13485 Quality Management Systems
Validation Engineer
Guilford, CT · Hybrid
... and FDA). * Collates, analyzes, summarizes, and interprets validation protocol results into ... Previous experience working with conventional inspection and measurement equipment, preferred.
Validation Engineer
Guilford, CT · Hybrid
... and FDA). * Collates, analyzes, summarizes, and interprets validation protocol results into ... Previous experience working with conventional inspection and measurement equipment, preferred.
Validation Engineer
Guilford, CT · On-site
... and FDA). * Collates, analyzes, summarizes, and interprets validation protocol results into ... Previous experience working with conventional inspection and measurement equipment, preferred.
Validation Engineer
Guilford, CT · On-site
... and FDA). * Collates, analyzes, summarizes, and interprets validation protocol results into ... Previous experience working with conventional inspection and measurement equipment, preferred.
Validation Engineer
Guilford, CT · Hybrid
... and FDA). * Collates, analyzes, summarizes, and interprets validation protocol results into ... Previous experience working with conventional inspection and measurement equipment, preferred.
Quick apply
Validation Engineer
Guilford, CT · Hybrid
... and FDA). * Collates, analyzes, summarizes, and interprets validation protocol results into ... Previous experience working with conventional inspection and measurement equipment, preferred.
Validation Engineer
Guilford, CT · Hybrid
... and FDA). * Collates, analyzes, summarizes, and interprets validation protocol results into ... Previous experience working with conventional inspection and measurement equipment, preferred.
Validation Engineer
Guilford, CT · Hybrid
... and FDA). * Collates, analyzes, summarizes, and interprets validation protocol results into ... Previous experience working with conventional inspection and measurement equipment, preferred.
Produce Inspection Team Leader, Distribution Center
Cheshire, CT · On-site
$77K - $132K/yr
OSHA, FMLA, Americans with Disabilities Act (ADA), Department of Labor, Health and Sanitation, FDA ... Experience as a Produce Inspector (1 year) The wage range for this position is $77,175.00-$132,300 ...
Produce Inspection Team Leader, Distribution Center
Cheshire, CT · On-site
$77K - $132K/yr
OSHA, FMLA, Americans with Disabilities Act (ADA), Department of Labor, Health and Sanitation, FDA ... Experience as a Produce Inspector (1 year) The wage range for this position is $77,175.00-$132,300 ...
Manager- Global CAPA System
Trumbull, CT · On-site
... FDA QMSR, and EU MDR. * Experience supporting regulatory inspections, notified body audits, and internal quality audits, including CAPA-related observation remediation. * Proficiency with electronic ...
Manager- Global CAPA System
Trumbull, CT · On-site
... FDA QMSR, and EU MDR. * Experience supporting regulatory inspections, notified body audits, and internal quality audits, including CAPA-related observation remediation. * Proficiency with electronic ...
Produce Inspection Team Leader, Distribution Center
Cheshire, CT · On-site
$77K - $132K/yr
OSHA, FMLA, Americans with Disabilities Act (ADA), Department of Labor, Health and Sanitation, FDA ... Experience as a Produce Inspector (1 year) The wage range for this position is $77,175.00-$132,300 ...
Produce Inspection Team Leader, Distribution Center
Cheshire, CT · On-site
$77K - $132K/yr
OSHA, FMLA, Americans with Disabilities Act (ADA), Department of Labor, Health and Sanitation, FDA ... Experience as a Produce Inspector (1 year) The wage range for this position is $77,175.00-$132,300 ...
Produce Inspection Team Leader, Distribution Center
Cheshire, CT · On-site
$77K - $132K/yr
OSHA, FMLA, Americans with Disabilities Act (ADA), Department of Labor, Health and Sanitation, FDA ... Experience as a Produce Inspector (1 year) The wage range for this position is $77,175.00-$132,300 ...
Produce Inspection Team Leader, Distribution Center
Cheshire, CT · On-site
$77K - $132K/yr
OSHA, FMLA, Americans with Disabilities Act (ADA), Department of Labor, Health and Sanitation, FDA ... Experience as a Produce Inspector (1 year) The wage range for this position is $77,175.00-$132,300 ...
... and FDA/MQSA guidelines and policies. * 2.1 Conducts daily inspection of mammographic equipment, Ultrasound machines (where applicable), procedural equipment, and supporting RIS systems, PenRad ...
... and FDA/MQSA guidelines and policies. * 2.1 Conducts daily inspection of mammographic equipment, Ultrasound machines (where applicable), procedural equipment, and supporting RIS systems, PenRad ...
Fda Inspector information
See Connecticut salary details
$23.3K - $29.7K
3% of jobs
$29.7K - $36.2K
16% of jobs
$37.8K is the 25th percentile. Wages below this are outliers.
$36.2K - $42.6K
23% of jobs
The median wage is $44.6K / yr.
$42.6K - $49.1K
27% of jobs
$53.2K is the 75th percentile. Wages above this are outliers.
$49.1K - $55.5K
10% of jobs
$55.5K - $62K
4% of jobs
$62K - $68.4K
5% of jobs
$68.4K - $74.8K
2% of jobs
$74.8K - $81.3K
2% of jobs
$81.3K - $87.7K
2% of jobs
$87.7K - $94.2K
5% of jobs
$23.3K
$52.3K
$94.2K
How much do fda inspector jobs pay per year?
As of Aug 12, 2026, the average yearly pay for fda inspector in Connecticut is $52,263.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,600.00 and $60,400.00 per year, depending on experience, location, and employer.
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.
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.
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 the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.
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 are the most commonly searched types of Fda Inspector jobs in Connecticut? The most popular types of Fda Inspector jobs in Connecticut are:
What are popular job titles related to Fda Inspector jobs in Connecticut? For Fda Inspector jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Connecticut look for? The top searched job categories for Fda Inspector jobs in Connecticut are:
Contractor
Re-posted 24 days ago
Onsite Women's Health rating
7.0
Based on 5 frontline employees who took The Breakroom Quiz
Job description
Description
PER DIEM OPPORTUNITIES AVAILABLE
Onsite Women's Health is on a mission to improve women's healthcare.
In partnership with forward-thinking providers across the country, Onsite Women's Health offers comprehensive mammography services with clinical expertise, innovative technology, and proprietary protocols that delivers personalized, convenient breast care for the patient.
Convenience drives compliance, and compliance saves lives.
Convenience is critical to ensure that most women have time to remain compliant with their breast care. By offering mammography and breast care within the patient's primary care or OB/GYN practice and scheduling appointments in coordination with an annual exam, compliance is easier to accomplish.
The Opportunity
The OWH program is unparalleled, making breast cancer screening more convenient for women.
Do you want a flexible work schedule?
Can you be available to cover on a moment's notice?
Do you want to experience different office environments?
Then come to Onsite Women's Health as a Per Diem Technologist!
See yourself here.
At Onsite we don't work weekends or after hours and offer the opportunity to use the latest 3D tomosynthesis digital mammography equipment in an OB/Gyn office environment.
If you are an experienced mammographer, someone who can work independently and wants to have an impact on each and every patient, join us as a Per Diem.
What do you need to be the right candidate for this role?
What are your responsibilities?
Exceptional compensation for the right candidate!
Experience:
License:
EOE M/F/V/H
PER DIEM OPPORTUNITIES AVAILABLE
Onsite Women's Health is on a mission to improve women's healthcare.
In partnership with forward-thinking providers across the country, Onsite Women's Health offers comprehensive mammography services with clinical expertise, innovative technology, and proprietary protocols that delivers personalized, convenient breast care for the patient.
Convenience drives compliance, and compliance saves lives.
Convenience is critical to ensure that most women have time to remain compliant with their breast care. By offering mammography and breast care within the patient's primary care or OB/GYN practice and scheduling appointments in coordination with an annual exam, compliance is easier to accomplish.
The Opportunity
The OWH program is unparalleled, making breast cancer screening more convenient for women.
Do you want a flexible work schedule?
Can you be available to cover on a moment's notice?
Do you want to experience different office environments?
Then come to Onsite Women's Health as a Per Diem Technologist!
See yourself here.
At Onsite we don't work weekends or after hours and offer the opportunity to use the latest 3D tomosynthesis digital mammography equipment in an OB/Gyn office environment.
If you are an experienced mammographer, someone who can work independently and wants to have an impact on each and every patient, join us as a Per Diem.
What do you need to be the right candidate for this role?
- Must be up to date on all CME credits.
- Must be very patient centric, compassionate, and computer savvy.
- Able to perform a variety of technical activities associated with the performance of screening and diagnostic mammography procedures.
- Flexible with the ability to multi-task.
- Willing to cover on a moment's notice.
What are your responsibilities?
- Specializes in the production of screening and diagnostic mammograms for the detection of breast cancers and lesions.
- Responsible for the initial and ongoing success of the mammography service in the practice in which one works. Assist practice in any and all ways possible to be sure all eligible age-appropriate patients have annual screening mammograms.
- Prepares patients for the mammographic procedure.
- Explains procedures to the patient to reduce anxieties and obtain patient cooperation.
- Moves mammographic equipment to specific positions and adjusts controls to set exposure factors based on knowledge of radiographic exposure techniques and protocols.
- Practices radiation protection techniques by using beam restrictive devices, patient shielding skills.
- Follows prescribed safety standards in operating all required equipment.
- Examines digital images for image quality.
- Ensures equipment is in proper working order at all times.
- Performs all required QA testing required to comply with MQSA, ACR and State requirements/regulations.
- Maintains patient confidentiality at all times.
- Processes routine paperwork and all required data entry.
- Participates in professional development activities and maintains professional affiliations.
- Prepares all required reports and data pursuant to MQSA and State requirements.
- Assists the Radiologist with QA/QC reporting.
- Performs all mammography tracking following MQSA guidelines and requirements.
- Maintains all QA documents necessary to exceed Annual FDA Inspection requirements.
- Is responsible for obtaining and maintaining ACR accreditation.
Exceptional compensation for the right candidate!
Experience:
- Mammography: 2 years (Required)
License:
- ARRT (Required)
EOE M/F/V/H
What Onsite Women's Health employees say
Hours and flexibility
Workplace
Get the full story on Breakroom
About Onsite Women's Health
Sourced by ZipRecruiter
Industry
Health care and social assistance
Company size
201 - 500 Employees
Headquarters location
Nashville, TN, US
Year founded
2008