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Fda Inspector Jobs in Pittsburgh, PA (NOW HIRING)

Corporate Supply Chain

Supply Specialist

Pittsburgh, PA · On-site

The items can contain FDA legend medication under the supervision of the Director of Pharmacy. Will ... Unload equipment, inspect verifies, accept or reject supplies and materials from delivery trucks ...

UPMC Senior Communities

Supply Specialist

Pittsburgh, PA · On-site

$18.79 - $28.03/hr

The items can contain FDA legend medication under the supervision of the Director of Pharmacy. Will ... Unload equipment, inspect verifies, accept or reject supplies and materials from delivery trucks ...

UPMC Senior Communities

Supply Specialist

Pittsburgh, PA · On-site

$19.60 - $30.25/hr

The items can contain FDA legend medication under the supervision of the Director of Pharmacy. Will ... Unload equipment, inspect verifies, accept or reject supplies and materials from delivery trucks ...

Corporate Supply Chain

Supply Specialist

Pittsburgh, PA · On-site

The items can contain FDA legend medication under the supervision of the Director of Pharmacy. Will ... Unload equipment, inspect verifies, accept or reject supplies and materials from delivery trucks ...

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Showing results 21-40

All JobsFda Inspector JobsFda Inspector Jobs in Pittsburgh, PA

Fda Inspector information

See Pittsburgh, PA salary details

$23.8K

$53.3K

$96.1K

How much do fda inspector jobs pay per year?

As of Aug 22, 2026, the average yearly pay for fda inspector in Pittsburgh, PA is $53,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,400.00 and $61,600.00 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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What job categories do people searching Fda Inspector jobs in Pittsburgh, PA look for?

The top searched job categories for Fda Inspector jobs in Pittsburgh, PA are:

What cities near Pittsburgh, PA are hiring for Fda Inspector jobs?

Cities near Pittsburgh, PA with the most Fda Inspector job openings:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Pittsburgh, PA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $53,336 per year, or $25.6 per hour.

Part Time Clinical Research Coordinator

SerenaGroup

Monroeville, PA • On-site

$53K - $58K/yr

Part-time

Re-posted 9 days ago

Job description

Job Type
Part-time
Description
The Clinical Research Coordinator (CRC) at SerenaGroup plays a critical role in the execution of clinical trials focused on advanced wound care and hyperbaric medicine. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory guidelines, and supporting high-quality patient care and data integrity throughout the study lifecycle.
The CRC will work collaboratively with Principal Investigators, Clinical Trial Leads, sponsors, and cross-functional teams to ensure studies are conducted efficiently, ethically, and in alignment with SerenaGroup's commitment to evidence-based care and improved patient outcomes.
Key Responsibilities
Study Coordination & Execution
  • Coordinate and manage day-to-day clinical trial activities from study start-up through close-out
  • Schedule and conduct study visits in accordance with protocol requirements
  • Ensure proper informed consent is obtained and documented for all study participants
  • Maintain accurate and up-to-date study documentation, including regulatory binders and source documents

Patient Care & Engagement
  • Identify, recruit, and screen eligible patients for clinical trials
  • Educate patients on study protocols, procedures, and expectations
  • Monitor patient safety and report adverse events in accordance with regulatory requirements

Data Management & Compliance
  • Accurately collect, record, and enter study data into electronic data capture (EDC) systems
  • Perform source data verification (SDV) and ensure data integrity and completeness
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, and SerenaGroup SOPs

Collaboration & Communication
  • Serve as a liaison between investigators, sponsors, CROs, and internal teams
  • Support monitoring visits, audits, and regulatory inspections
  • Communicate effectively with cross-functional teams to ensure study milestones are met

Qualifications
Education & Experience
  • Bachelor's degree in life sciences, healthcare, or related field preferred
  • 1-3 years of experience in clinical research or healthcare setting (wound care experience a plus)
  • Experience working with clinical trial protocols and regulatory requirements preferred

Skills & Competencies
  • Strong organizational and time management skills
  • High attention to detail and accuracy in documentation
  • Excellent interpersonal and communication skills
  • Ability to manage multiple studies and priorities in a fast-paced environment
  • Proficiency in EDC systems and Microsoft Office Suite

Preferred Qualifications
  • Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA)
  • Experience in wound care, hyperbaric medicine, or related therapeutic areas
  • Familiarity with clinical trial start-up and regulatory submissions

Salary Description
$53,000-$58,000

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