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Fda Inspector Jobs in Philadelphia, PA (NOW HIRING)

... FDA-regulated micronization facility. This position involves monitoring production processes, conducting inspections, and collaborating with cross-functional teams to maintain high standards.

QC Lab Technician

Moorestown, NJ ยท On-site

$20 - $21/hr

Collaborate with the Quality Assurance team to address non-conformities. * Assist during internal and external audits, including FDA inspections. * Ensure compliance with cGMP (current Good ...

Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...

Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...

The impact of the quality inspection process directly impacts company compliance to regulatory ... General knowledge of FDA regulations related to cGMPs is desired. General knowledge of quality ...

Digital Systems Validation Lead

Wayne, PA ยท Hybrid

$116K - $130K/yr

Familiarity supporting FDA inspections, notified body reviews, and internal or external quality audits * Understanding of SDLC and Agile development environments and how validation integrates within ...

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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 Jul 1, 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.

How much do FDA drug investigators make?

FDA drug investigators typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and level of responsibility. They often hold a bachelor's degree in a relevant field and may require specialized training or certifications related to regulatory compliance and inspection procedures.

What types of facilities or products do FDA Inspectors typically 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.

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

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 type of inspector gets paid the most?

Among FDA inspectors, senior or specialized inspectors, such as those overseeing complex manufacturing facilities or with advanced certifications, tend to earn higher salaries. Experience, certifications, and geographic location also influence pay levels for FDA inspectors. Generally, inspectors with specialized skills or leadership roles earn the most in this field.

Is it hard to get a job at FDA?

Becoming an FDA inspector can be competitive due to strict qualification requirements, including relevant experience, education, and passing civil service exams. Candidates often need a background in science, public health, or regulatory compliance, along with strong attention to detail and communication skills. The hiring process can be lengthy and involves multiple steps such as interviews and background checks.

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 manufacturing. They must pass a written exam and a background check, and often complete on-the-job training or specialized FDA training programs. Certification or licensing is not required but can enhance prospects.

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 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 cities near Philadelphia, PA are hiring for Fda Inspector jobs? Cities near Philadelphia, PA with the most Fda Inspector job openings:

QUALITY ASSURANCE ASSOCIATE/ Medical Device

jalet associes

Philadelphia, PA โ€ข On-site

Full-time

Posted 18 days ago


Key responsibilities

  • Write and review SOPs, technical data forms, and quality documents related to quality assurance.

  • Assist in carrying out internal quality audits and perform investigations on non-conformances and customer complaints.

  • Maintain control documents in Quality Assurance and ensure their distribution to different departments.


Job description

Company Description
Our clientis a medical device company dedicated to offering innovative solutions for treatment of chronic heart failure. The Company's developments are based on its proprietary technology for administrating Cardiac Contractility Modulation therapy.
Job Description
  • Write and review of SOPs and other quality assiuance related technical data forms and quality documents
  • proper maintenance of control documents in Quality Assurance
  • Control documents to differents departments
  • Review validation protocols for GMP compliance
  • Assist in carrying out internal quality audits on company systems and documentations
  • perform investigations on non-conformances and customer complaint close out and corrective actions
  • Audit on-going vendors, systems and documents to assure quality assurance compliance with regard to all internal procedures as well as regulatory guidelines
  • Provide GCP/ QA support and avdvice to internal and external clients
  • Ensure the timely and effective follow up to all identified or assigned quality issues
  • Maintains and demonstrates understanding of global standards, regulation and regulatory bodies to include but not limited to ISO13485, 21FR; part 820 AIMD
  • Assist in the maintenance ogf Quality Management System under direction of Director, Quality Assurance
  • Participate in Mock inspections for FDA inspection preparation

Qualifications
Ability to work independently with little or no supervision
Exeptional oral and written communication capabilities
Advance computer knowledge in MS Office programs
Bachelors's Dregree in related field
4-6 years related experience
Experience working in regulated environment with medical devices
Experience with FDA inspections and /or Notified Bodies Audits desirable
Additional Information
All your information will be kept confidential according to EEO guidelines.