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Fda Inspector Jobs in Philadelphia, PA (NOW HIRING)

Doist

Head of US Quality Assurance

Pennington, NJ · On-site

$190 - $250/hr

Ensure continuous regulatory compliance and maintain inspection readiness for FDA, customer, and other regulatory inspections and audits. * Lead customer quality activities, including Quality ...

New

Smiths Machine

Quality Engineer {SE}

Huntingdon Valley, PA · On-site

$70K - $91K/yr

... 13485 and FDA quality system regulation requirements * Evaluates changes to design and/or ... Develops, documents, and validates inspection and test methods to support design control, in ...

Ocugen Inc

TMF Lead

Malvern, PA · On-site

$32.75 - $45/hr

Maintain ongoing inspection readiness for all assigned studies; coordinate document retrieval and responses during sponsor audits and regulatory inspections (FDA, EMA, MHRA, and other health ...

OCUGEN OPCO INC

TMF Lead

Malvern, PA

$32.75 - $45/hr

Maintain ongoing inspection readiness for all assigned studies; coordinate document retrieval and responses during sponsor audits and regulatory inspections (FDA, EMA, MHRA, and other health ...

Actalent

Validation Manager

Cherry Hill, NJ · On-site

$90K - $155K/yr

... FDA regulations, and pharmaceutical industry standards. * Collaborate with cross-functional teams ... Maintain a high standard of inspection readiness by ensuring documentation, processes, and systems ...

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All JobsFda Inspector JobsFda Inspector Jobs in Philadelphia, PA

Fda Inspector information

See Philadelphia, PA salary details

$24.7K

$55.4K

$99.9K

How much do fda inspector jobs pay per year?

As of Aug 22, 2026, the average yearly pay for fda inspector in Philadelphia, PA is $55,438.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,800.00 and $64,100.00 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 popular job titles related to Fda Inspector jobs in Philadelphia, PA?

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

What job categories do people searching Fda Inspector jobs in Philadelphia, PA look for?

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

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

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

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Philadelphia, PA as of August 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $55,438 per year, or $26.7 per hour.

System Level Review (SLR) & Audit Trail Review (ATR) Consultant - GxP Laboratory Systems

Alphanumeric

Collegeville, PA • On-site

$70 - $85/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago

Job description

System Level Review (SLR) & Audit Trail Review (ATR) Consultant - GxP Laboratory Systems
Location: Collegeville, PA (100% Onsite)
Pay: $70-85/hour W2 (depending on experience)
Benefits: Medical, Dental, Vision, 401(k), PTO, Paid Holidays, and more.
Alphanumeric is seeking an experienced System Level Review (SLR) & Audit Trail Review (ATR) Consultant to support a leading global pharmaceutical organization at its Collegeville, PA campus.
This role is ideal for a Computerized System Validation (CSV) professional with hands-on experience supporting laboratory equipment and computerized systems in a regulated GxP environment. The successful candidate will perform System Level Reviews, Audit Trail Reviews, and Data Integrity assessments while ensuring laboratory systems remain compliant, inspection-ready, and aligned with FDA regulatory expectations.
Candidates with experience performing Periodic Reviews, Computerized System Reviews, or equivalent laboratory system compliance assessments are encouraged to apply.
What you'll be doing
  • Perform System Level Reviews (SLRs) for laboratory equipment and computerized systems.
  • Execute Audit Trail Reviews (ATRs) to evaluate system compliance, electronic records, and data integrity.
  • Assess laboratory systems for compliance with GxP, FDA 21 CFR Part 11, and applicable regulatory requirements.
  • Review audit trails, electronic records, user access, security controls, system configurations, and lifecycle documentation.
  • Identify data integrity risks, compliance gaps, and opportunities for remediation.
  • Author and review validation documentation, including risk assessments, validation plans, protocols, reports, periodic reviews, and change controls.
  • Support Computerized System Validation (CSV) activities throughout the system lifecycle.
  • Partner with Quality Assurance, Validation, Laboratory Operations, Engineering, and IT teams to ensure systems remain in a validated state.
  • Support internal audits, regulatory inspections, and inspection readiness initiatives.
  • Ensure validation deliverables meet established quality standards and project timelines.

Job Requirements
Required Qualifications
  • Bachelor's degree in Engineering, Computer Science, Chemistry, Biology, Life Sciences, or a related technical discipline.
  • Minimum 5 years of experience supporting GxP-regulated pharmaceutical, biotechnology, or life sciences environments.
  • Hands-on experience performing Computerized System Validation (CSV).
  • Experience conducting System Level Reviews (SLRs), Periodic Reviews, and/or Audit Trail Reviews (ATRs) for laboratory equipment or computerized systems.
  • Strong knowledge of:
    • GxP
    • FDA 21 CFR Part 11
    • Data Integrity (ALCOA+)
    • Electronic Records and Electronic Signatures
    • Change Control and Risk Assessment
  • Experience supporting laboratory computerized systems and laboratory equipment.
  • Strong technical writing, documentation, and communication skills.

Preferred Experience
Experience with one or more of the following systems is highly desirable:
  • Waters Empower
  • LabWare LIMS
  • LabVantage
  • Chromeleon
  • OpenLab
  • Electronic Laboratory Notebooks (ELN)
  • Veeva
  • Kneat
  • ValGenesis

Preferred Skills
  • Computerized System Validation (CSV)
  • Data Integrity
  • Audit Trail Reviews
  • System Level Reviews
  • Laboratory Compliance
  • Risk Assessment
  • CAPA
  • Change Control
  • Root Cause Analysis
  • GAMP 5
  • Good Manufacturing Practice (GMP)
  • Laboratory Information Management Systems (LIMS)

Why Join Us?
This is an opportunity to support highly visible compliance initiatives within a global pharmaceutical organization. You'll work alongside cross-functional Quality, Validation, Engineering, and Laboratory teams on projects that directly impact regulatory compliance, data integrity, and inspection readiness.
Please Note: This is a 100% onsite position located in Collegeville, PA. Candidates must be authorized to work in the United States on a W2 basis. We are unable to accept third-party candidates or provide sponsorship now or in the future.

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