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Fda Investigator Jobs in Raleigh, NC (NOW HIRING)

Medasource

GMP Compliance Investigator

Durham, NC · On-site

This individual will play a key role in maintaining compliance with FDA regulations and applicable accreditation standards by leading investigations, authoring quality documentation, and partnering ...

RX2 Solutions

Pharmacist in Charge

Apex, NC · On-site

$43.75 - $53.50/hr

July/August 2026 The Vanguard Utility Corporation is launching a new FDA-registered 503B ... When issues arise, you will lead investigations with clarity and discipline, ensuring corrective ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Prepare and support FDA submissions in partnership with regulatory experts and investigators. * Manage investigational products, including receipt, storage, accountability, tracking, and participant ...

MedPharm

Sr. Process Engineer/Sr. Scientist

Durham, NC · On-site

$94K - $121K/yr

Technical support in investigations for deviations, OOS/OOT results, complaints, and CAPAs related ... Ensure compliance with cGMP, FDA, EMA, ICH, and internal quality standards. Required Qualifications

Elevait Solutions

Calibration Technician

Morrisville, NC · On-site

$36 - $37/hr

Experience investigating and completing deviations and CAPAs in a GxP environment * Working knowledge of calibration methodology, tolerances, and FDA regulations * Experience documenting calibration ...

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Fda Investigator information

See Raleigh, NC salary details

$31.1K

$73.2K

$127.3K

How much do fda investigator jobs pay per year?

As of Aug 26, 2026, the average yearly pay for fda investigator in Raleigh, NC is $73,217.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,000.00 and $95,700.00 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 Raleigh, NC?

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

What job categories do people searching Fda Investigator jobs in Raleigh, NC look for?

The top searched job categories for Fda Investigator jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Fda Investigator jobs?

Cities near Raleigh, NC with the most Fda Investigator job openings:

Fda Investigator jobs near you
Infographic showing various Fda Investigator job openings in Raleigh, NC as of August 2026, with employment types broken down into 92% Full Time, 7% Part Time, and 1% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $73,217 per year, or $35.2 per hour.

GMP Compliance Investigator

Durham, NC • On-site

Medasource
Health Care and Social Assistance • 201 - 500 employees
Learn more about Medasourceexternal

Contractor

Posted 14 days ago

Job description

GMP Compliance Investigator - Equipment & Facilities
Overview
Our client is seeking a GMP Compliance Investigator - Equipment & Facilities to support a GMP manufacturing laboratory focused on advanced cellular therapies. This individual will play a key role in maintaining compliance with FDA regulations and applicable accreditation standards by leading investigations, authoring quality documentation, and partnering closely with Manufacturing and Quality teams.
This is a highly collaborative role for someone with strong GMP quality experience, exceptional technical writing skills, and the ability to manage complex investigations from initiation through closure.
Responsibilities
  • Develop, revise, and maintain Standard Operating Procedures (SOPs) to ensure compliance with FDA and applicable regulatory requirements.
  • Author and manage change controls related to SOP updates and manufacturing process improvements.
  • Edit batch records and manufacturing documentation as needed.
  • Initiate, investigate, author, and close deviations, CAPAs, investigations, and quality memos.
  • Partner with Manufacturing and Quality teams to investigate manufacturing events and drive timely closure of quality records.
  • Serve as the primary author for equipment and facility-related deviation investigations.
  • Attend meetings with equipment vendors and internal stakeholders to gather information supporting investigations.
  • Author validation documentation, including IQ, OQ, and PQ protocols, equipment assessments, and validation reports.
  • Manage deviation, CAPA, and change control timelines to support on-time batch release.
  • Perform failure mode analysis and root cause investigations.
  • Support batch release activities from a compliance perspective.
  • Ensure compliance with FDA regulations and applicable accreditation standards.
  • Train and educate personnel on updated procedures, SOPs, quality systems, and compliance requirements.
  • Assist during FDA, accreditation, sponsor, and regulatory inspections, including responses to audit observations.
  • Monitor Quality Agreements to ensure sponsor notification requirements are met.
  • Participate in continuous improvement initiatives to optimize quality systems and documentation processes.
Preferred Qualifications
  • Experience working in a Quality Assurance or GMP Compliance function within an FDA-regulated manufacturing environment.
  • Experience supporting deviations, investigations, CAPAs, and change controls.
  • Strong technical writing skills with experience authoring investigation reports and SOPs.
  • Experience participating in FDA inspections, regulatory audits, and sponsor audits.
  • Experience with electronic Quality Management Systems (QMS).
  • Project management experience.
  • Strong analytical and root cause investigation skills.
  • Excellent written and verbal communication skills.
  • Strong organizational skills with exceptional attention to detail.
  • Ability to work independently while collaborating effectively across cross-functional teams.
Minimum Qualifications
Education
  • Bachelor's degree in Biology, Life Sciences, or a related scientific discipline.

Experience
  • Minimum of 6 years of Quality Assurance, Quality Systems, or GMP Compliance experience within a regulated manufacturing environment.
  • A Master's degree in a related field may substitute for two years of experience.

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