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Fda Inspector Jobs in Connecticut (NOW HIRING)

ICU Medical

Senior QA Inspector

Southington, CT · On-site

The Sr. QA Inspector enforces GMP compliance as outlined in internal BOPs. The individual is ... These elements include FDA, EPA, OSHA, ISO, EEOC and Company policies relative to the manufacture ...

ICU Medical, Inc.

Senior QA Inspector

Southington, CT · On-site

$55 - $75/hr

These elements include FQA, EPA, FDA, OSHA, ISO, EEPC and Company policies relative to the manufacture of product, lot control requirements, documentation requirements, housekeeping, preventative ...

Ametek

Senior Quality Engineer

Bridgeport, CT · On-site

$90K - $122K/yr

You will support and enforce the development of internal systems and procedures to meet ISO standards and FDA quality system regulations. You will develop and implement inspection/validation ...

AMETEK, Inc.

Senior Quality Engineer

Bridgeport, CT · On-site

$90 - $115/hr

You will support and enforce the development of internal systems and procedures to meet ISO standards and FDA quality system regulations. You will develop and implement inspection/validation ...

Ametek

Senior Quality Engineer

Bridgeport, CT · On-site

$90K - $122K/yr

You will support and enforce the development of internal systems and procedures to meet ISO standards and FDA quality system regulations. You will develop and implement inspection/validation ...

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Fda Inspector information

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$23.3K

$52.3K

$94.2K

How much do fda inspector jobs pay per year?

As of Sep 2, 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 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 the most commonly searched types of Fda Inspector jobs in Connecticut?

The most popular types of Fda Inspector jobs in Connecticut are:

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For Fda Inspector jobs in Connecticut, the most frequently searched job titles are:

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Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Connecticut as of August 2026, with employment types broken down into 86% Full Time, 9% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $52,263 per year, or $25.1 per hour.

Senior QA Inspector

ICU Medical

Southington, CT • On-site

Full-time

Posted 26 days ago

ICU Medical rating

7.8

Company rating: 7.8 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

154th of 545 rated manufacturers

Job description


Position Summary
The Sr. QA Inspector performs testing and inspection of sub-assemblies, final product, commodities, GMP, BOP, safety compliance audits. The Sr. QA Inspector enforces GMP compliance as outlined in internal BOPs. The individual is primarily responsible for testing, inspection and release of product and product components and commodities. The individual records and reports results to provide information necessary to assure that product has been manufactured in accordance with established quality standards.
Essential Duties & Responsibilities
  • Initiate change requests, BOPs, EPWOs, deviations, NCMRs
  • Close-out audit work orders and commodity release
  • Complete product and part inspection
  • Complete sample pulling
  • Complete labeling inspection and control
  • Provide line clearance approval
  • Monitor GMP practice
  • Quarantine and release quarantined materials
  • Train new employees and team on GMP and BOPs
  • Must perform defect tracking, monthly reporting and data entry
  • Complete test requests
  • Ensures departmental compliance to all Federal, State, Local and Company regulatory requirements. These elements include FDA, EPA, OSHA, ISO, EEOC and Company policies relative to the manufacture of product, lot control requirements, documentation requirements, housekeeping, preventative maintenance, calibration, associate training and safety (equipment, associate and material).
  • Perform these and other duties as necessary or required, the inclusion of which will not alter the basic scope of the position
  • Work on special projects as they arise
  • Actively demonstrating support through interactions with solid communication skills, attitude, dedication, commitment, respect, pride and trust.

Knowledge, Skills & Qualifications
  • Excellent Mathematical knowledge

Education and Experience
  • Must be 18 years of age
  • High School Diploma or GED required
  • Four years previous experience as an MQA or QA Inspector preferred
  • Experience with medical devices/pharmaceutical GMPs preferred

Physical Requirements and Work Environment
  • While performing the duties of this job, the employee is regularly required to talk or hear.
  • This job operates in a clean room environment.
  • While performing the duties of this job, the employee may be required to sit or stand for the duration of the shift
  • Must be able to repetitively move and lift objects of up to 20 lbs
  • Typically requires travel less than 5% of the time

About Us
ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.
With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.
We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you:
  • Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
  • The industry's broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
  • IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
  • Significant US IV solutions manufacturing and supply capabilities.

ICU Medical EEO Statement:
ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.
If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.
ICU Medical EEO Policy Statement
Know Your Rights: Workplace Discrimination is Illegal Poster
ICU Medical CCPA Notice to Job Applicants

What ICU Medical employees say

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About ICU Medical

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

San Clemente, CA, US

Year founded

1984

Social media

Twitter

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