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Fda Investigator Jobs in Delaware (NOW HIRING)

Hologic, Inc.

Product Quality Engineer 3

Newark, DE · On-site

$85.30 - $133/hr

In this role, you will investigate product performance issues and customer complaints, conduct risk ... Skills * Working knowledge of FDA Quality System Regulations, especially Design Control ...

Hologic Inc.

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device ... Analytical skills to support and lead investigations, including CAPAs, nonconformances, and other ...

Hologic

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device ... Analytical skills to support and lead investigations, including CAPAs, nonconformances, and other ...

Hologic

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device ... Analytical skills to support and lead investigations, including CAPAs, nonconformances, and other ...

Hologic Inc.

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device ... Analytical skills to support and lead investigations, including CAPAs, nonconformances, and other ...

QPS, LLC

Senior Specialist, Sample Management QC

Newark, DE · On-site

$49K - $57K/yr

Perform QC of Sample Receipt records against an electronic database to ensure they comply with FDA ... Investigator * Compile and/or perform QC on Sample Receipt tables prior to submission to QA * QC ...

QPS, LLC

Senior Specialist, Sample Management QC

Newark, DE · On-site

$49K - $57K/yr

Perform QC of Sample Receipt records against an electronic database to ensure they comply with FDA ... Investigator * Compile and/or perform QC on Sample Receipt tables prior to submission to QA * QC ...

Hologic

Product Quality Engineer 3

Newark, DE · On-site

$85K - $133K/yr

In this role, you will investigate product performance issues and customer complaints, conduct risk ... Skills * Working knowledge of FDA Quality System Regulations, especially Design Control ...

Hologic Inc.

Product Quality Engineer 3

Newark, DE · On-site

$85K - $133K/yr

In this role, you will investigate product performance issues and customer complaints, conduct risk ... Skills * Working knowledge of FDA Quality System Regulations, especially Design Control ...

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

Experience leading laboratory investigations, troubleshoot instrumentation, and author technical reports. * Strong understanding of USP, EP, JP, ICH, FDA, and cGMP requirements applicable to raw ...

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

Experience leading laboratory investigations, troubleshoot instrumentation, and author technical reports. * Strong understanding of USP, EP, JP, ICH, FDA, and cGMP requirements applicable to raw ...

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Showing results 21-40

All JobsFda Investigator JobsFda Investigator Jobs in Delaware

Fda Investigator information

See Delaware salary details

$32K

$75.4K

$131.1K

How much do fda investigator jobs pay per year?

As of Sep 5, 2026, the average yearly pay for fda investigator in Delaware is $75,389.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $98,600.00 per year, depending on experience, location, and employer.

What does an FDA Investigator do?

An FDA Investigator is responsible for inspecting facilities that manufacture, process, or distribute regulated products, including food, drugs, medical devices, and cosmetics. They ensure compliance with federal regulations, identify violations, and document findings through reports. Investigators may also collect samples, review records, and participate in enforcement actions when necessary. Their work helps protect public health by ensuring the safety, efficacy, and quality of products entering the market.

What does a typical day look like for an FDA Investigator?

A typical day for an FDA Investigator involves conducting on-site inspections of food, drug, medical device, or cosmetic manufacturers to ensure compliance with federal regulations. Investigators review production processes, collect samples, examine records, and interview facility staff to assess safety and quality standards. The role often includes significant report writing and follow-up activities to document findings and recommend corrective actions. While much of the work is independent, FDA Investigators also collaborate closely with colleagues, regulatory officials, and industry representatives to resolve issues and maintain public health standards.

What are the key skills and qualifications needed to thrive in the FDA Investigator position, and why are they important?

To thrive as an FDA Investigator, you need a background in science or public health, strong analytical skills, and often a bachelor's degree in a related field. Familiarity with regulatory databases, laboratory sampling equipment, and federal inspection protocols is typically required. Effective communication, meticulous attention to detail, and strong organizational skills help investigators excel in documenting findings and interacting with diverse stakeholders. These attributes are crucial for ensuring compliance with federal regulations and protecting public health.

How much money do FDA investigators make?

FDA investigators typically earn a median annual salary of around $70,000 to $90,000, depending on experience, location, and level of education. Entry-level investigators may start at lower salaries, while those with advanced certifications or extensive experience can earn higher wages, often with benefits such as health insurance and retirement plans.

How to become an FDA investigator?

To become an FDA investigator, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or pharmacy, along with experience in regulatory or scientific work. They must also pass the FDA's specialized training program and meet background check requirements. Strong analytical skills, attention to detail, and knowledge of regulatory guidelines are essential for this role.

What are popular job titles related to Fda Investigator jobs in Delaware?

For Fda Investigator jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Fda Investigator jobs in Delaware look for?

The top searched job categories for Fda Investigator jobs in Delaware are:

Fda Investigator jobs near you
Infographic showing various Fda Investigator job openings in Delaware as of August 2026, with employment types broken down into 89% Full Time, and 11% Part Time. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $75,389 per year, or $36.2 per hour.

Chemist (Pharmaceutical Manufacturing)

Synerfac Technical Staffing

Middletown, DE

$50K - $100K/yr

Full-time

Re-posted 4 hours ago

Job description

Job Summary
The Chemist is responsible for performing chemical analyses, testing raw materials, in-process samples, finished products, and stability samples to ensure compliance with company specifications, Good Manufacturing Practices (GMP), and regulatory requirements. The role supports manufacturing operations by maintaining product quality, investigating laboratory results, and ensuring accurate documentation.
Key Responsibilities
Perform chemical analysis of raw materials, intermediates, finished products, and stability samples using approved analytical methods.
Operate, calibrate, and maintain laboratory instruments such as HPLC, GC, UV-Vis Spectrophotometer, FTIR, pH meters, and analytical balances.
Prepare reagents, standards, and sample solutions according to established procedures.
Review and interpret analytical data, ensuring accuracy and compliance with specifications.
Document laboratory activities in accordance with Good Documentation Practices (GDP), Good Manufacturing Practices (GMP), and company Standard Operating Procedures (SOPs).
Investigate out-of-specification (OOS), out-of-trend (OOT), and laboratory deviations as required.
Assist in method validation, method transfer, verification, and analytical troubleshooting.
Participate in laboratory investigations, corrective and preventive actions (CAPA), and continuous improvement initiatives.
Ensure compliance with health, safety, environmental, and quality regulations.
Support internal and external audits by providing laboratory documentation and technical information.
Collaborate with Production, Quality Assurance, Validation, and Regulatory Affairs teams to resolve quality-related issues.
Maintain laboratory cleanliness, organization, and inventory of chemicals and laboratory supplies.
Qualifications:
Bachelor's degree in Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, or a related scientific discipline.
Previous experience in a pharmaceutical manufacturing or quality control laboratory is preferred.
Knowledge of GMP, GLP, FDA, ICH, and other applicable regulatory guidelines.
Experience with chromatographic and spectroscopic analytical techniques is an advantage.
Strong analytical, problem-solving, and organizational skills.
Proficiency in Microsoft Office and laboratory data management systems.
Excellent written and verbal communication skills.
Preferred Skills
Experience with HPLC, GC, FTIR, UV-Vis spectroscopy, and dissolution testing.
Familiarity with Laboratory Information Management Systems (LIMS).
Knowledge of analytical method validation and stability testing.
Ability to work independently and collaboratively in a cross-functional team.
Strong attention to detail and commitment to data integrity.
Working Conditions
Laboratory-based position within a pharmaceutical manufacturing facility.
May require shift work, overtime, or weekend work based on production requirements.
Requires the use of appropriate personal protective equipment (PPE) and adherence to laboratory safety protocols.
Key Performance Indicators (KPIs)
Timely completion of laboratory testing.
Accuracy and reliability of analytical results.
Compliance with GMP, SOPs, and regulatory requirements.
On-time completion of documentation and reports.
Successful participation in audits and quality improvement initiatives.
Synerfac Technical Staffing logo

About Synerfac Technical Staffing

Sourced by ZipRecruiter

Since 1987, Synerfac has served three groups, Our Clients, Our Candidates and Our Staff. We treat all three with equal importance because we recognize the synergy of success when one group succeeds, We all succeed. Synerfac is in the business of providing opportunities and adding value. We strive to create extraordinary experiences. For our clients we provide staffing services that enable them to focus on their core competencies which will add value to their businesses. For our employees we provide permanent and temporary assignments that complement their job skills and experience while providing professional and financial rewards. For our staff –we provide careers that are balanced, uplifting and carry the highest rewards by continually improving our business process. Our goal is to enhance the lives and enterprises of all those we touch to make them better off for having known us.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Cherry Hill, NJ, US

Social media

Twitter

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