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Fda Inspector Jobs in Raleigh, NC (NOW HIRING)

GRIFOLS, S.A.

Product Inspector (2nd shift)

Clayton, NC · On-site

A visual inspection of plasma units is also performed, removing any units which are unacceptable (e ... Two years' experience in Manufacturing, Pharmaceutical or other FDA licensed Industry is desirable.

Euromed Pharma Us Inc

Director of Quality US

Raleigh, NC · On-site

$130 - $200/hr

Represent the company during regulatory inspections (Authority and customer audits 2. Responsible Person (RP) * Ensure compliance with FDA, cGDP requirements and applicable regulations for wholesale ...

Euromed Pharma Us Inc

Director of Quality US

Raleigh, NC · On-site

$110K - $130K/yr

Represent the company during regulatory inspections (Authority and customer audits 2. Responsible Person (RP) * Ensure compliance with FDA, cGDP requirements and applicable regulations for wholesale ...

Euromed Pharma Us Inc

Director of Quality US

Raleigh, NC · On-site

$110K - $130K/yr

Represent the company during regulatory inspections (Authority and customer audits 2. Responsible Person (RP) * Ensure compliance with FDA, cGDP requirements and applicable regulations for wholesale ...

Euromed Pharma Us Inc

Director of Quality US

Raleigh, NC · On-site

$110K - $130K/yr

Represent the company during regulatory inspections (Authority and customer audits 2. Responsible Person (RP) * Ensure compliance with FDA, cGDP requirements and applicable regulations for wholesale ...

MedPharm

Cleaning Validation Engineer

Durham, NC · On-site

Maintain inspection readiness through documentation, deviation, and CAPA management * Support ... Strong knowledge of regulatory requirements (FDA, cGMP, ICH Q9, ASTM E2500, EU Annex 1, GAMP 5, ...

MedPharm

Cleaning Validation Engineer

Durham, NC · On-site

Maintain inspection readiness through documentation, deviation, and CAPA management * Support ... Strong knowledge of regulatory requirements (FDA, cGMP, ICH Q9, ASTM E2500, EU Annex 1, GAMP 5, ...

Kelly Services

Incoming Inspection Lead

Raleigh, NC

$80K - $110K/yr

Serve as the SME during FDA, EMA, and other regulatory inspections, including audit preparation and response activities. * Provide technical leadership, coaching, mentoring, and training for incoming ...

Kelly Services

QA Systems Specialist

Raleigh, NC

$76K - $110K/yr

... cGMP, FDA, and other applicable regulatory requirements. This role helps maintain inspection readiness by supporting quality systems, change control, audits, quality metrics, and continuous ...

Revlon Corporate

Director, Quality Control

Oxford, NC · On-site

... cGMP, FDA expectations, laboratory investigations, data integrity, analytical method validation, stability, and laboratory equipment systems. • Experience supporting regulatory inspections ...

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All JobsFda Inspector JobsFda Inspector Jobs in Raleigh, NC

Fda Inspector information

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$23.8K

$53.4K

$96.2K

How much do fda inspector jobs pay per year?

As of Aug 17, 2026, the average yearly pay for fda inspector in Raleigh, NC is $53,402.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,400.00 and $61,700.00 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.

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Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Raleigh, NC as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $53,402 per year, or $25.7 per hour.

Product Inspector (2nd shift)

GRIFOLS, S.A.

Clayton, NC • On-site

Other

Re-posted 29 days ago

Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Plasma Classification Certified Inspector
2nd Shift - Monday - Thursday 1:30pm - 12:00am
Position requires scanning and removal of unsuitable plasma units utilizing the Plasma Management System (SGP). A visual inspection of plasma units is also performed, removing any units which are unacceptable (e.g. damaged, broken port/tube, RBC, or backup sample rejections). Employee must be able to perform secondary verifications and Perform end of PU line clearances.
Responsibilities
  • Scanning of plasma units assigned to a PU utilizing a barcode reader.
  • Scanning of archive samples assigned to a SA utilizing a barcode reader.
  • Transferring units to a Sub-shipment during the PU process.
  • Entering "Statistics" during the PU process.
  • Sub-shipment verification at the end of the PU process.
  • "Blocking" of units which do not meet customer requirements.
  • Responsible for various rejections found during visual inspection.
  • Removal of unsuitable plasma units marked for removal in SGP during the PU process.
  • Able to maintain record accountability.
  • Able to perform job duties with minimum supervision.
  • Ability to follow written procedures.
  • Monitoring plasma time out of freezer
  • Department housekeeping and safety practices
  • Processing of unsuitable plasma units during any step of the plasma process.
  • Transfer of unsuitable plasma units (status 100) to correct reject inventory
  • Transferring units between PU/LOT to a PU.
  • Ability to consistently meet department average throughput.
  • Knowledge of SGP Status codes and Disposition Codes.
  • Knowledge of labeling Requirements.
  • Scanning of case/units to a 3rd party sale utilizing Disposition Module.
  • Scanning of case/units to a MDO process utilizing Disposition Module.
  • Completing the partial PU cases between PU's.
  • Line Clearance at the end of a Plasma Process.

Requirements
  • High School diploma or equivalent.
  • Two years' experience in Manufacturing, Pharmaceutical or other FDA licensed Industry is desirable.
  • Knowledge of cGMPs and Industry Standards.
  • Ability to follow "Standard Operating Procedures".
  • Possess good verbal and written communication skills.
  • Possess basic math skills (addition, subtraction, division, multiplication).
  • Basic Computer skills.

Occupational Demands
Work is performed in a manufacturing environment with rotating shifts. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to chemicals, electrical manufacturing equipment, hand tools and moving machinery. Exposure to high levels of noise and to extreme cold below 32*. Occasional entry into confined spaces requiring kneeling and squatting. Operates forklifts, tractors and power equipment. Personal protective equipment required such as protective eyewear, safety shoes, gloves and garments. Work is performed standing and walking for 6-8 hours per day. Bending and twisting neck and waist for 6-8 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement. Frequent moderate lifting and carrying of 15-44lbs. Frequent heavy lifting and carrying of 45lbs. with a maximum lift of 50lbs. Occasionally reaches above and below shoulder height. Hearing acuity essential. Color perception/discrimination, depth perception and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Frequently performs simple and routine tasks that vary little each day by following a set of written or oral instructions/procedures.
#BiomatUSA
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
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