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Fda Inspector Jobs in Philadelphia, PA (NOW HIRING)

Solesis

Validation Specialist II

Telford, PA · On-site

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 ...

Secant

Validation Specialist II

Telford, PA · On-site

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 ...

Penn Life Sciences

Be Seen First

Manager, Facilities & Engineering (Validation)

Langhorne, PA · On-site

$130K - $150K/yr

Experience supporting FDA inspections, pre-approval inspections, customer audits, or other regulatory assessments preferred. Education: * Bachelor's degree in Engineering or a related technical or ...

AstraZeneca

Manager, REMS

Wilmington, DE · On-site

Your work will ensure compliant, effective delivery across the REMS lifecycle-keeping programs inspection-ready, data-driven, and aligned with FDA expectations. You will partner closely with REMS ...

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Showing results 21-40

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.

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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.

Quality Control Inspector

Nevro Corp.

Eagleville, PA • On-site

Full-time

Re-posted 18 days ago

Job description

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.
Nevro Corp., a subsidiary of Globus Medical Inc., is a global medical device company focused on delivering comprehensive, life-changing solutions that continue to set the standard for enduring patient outcomes in the treatment of chronic pain. Nevro's comprehensive HFX™ spinal cord stimulation (SCS) platform includes the Senza® SCS system and support services for the treatment of chronic pain of the trunk and limb and painful diabetic neuropathy. Nevro also provides minimally invasive treatment options for patients suffering from chronic sacroiliac joint pain.
Position Summary:
The Quality Control Inspector is responsible for performing inspections at various stages of production of the product from raw material. This effort includes, but is not limited to, providing QA support, where needed, but not limited to QA Operations. This individual works with other quality control inspectors and engineers to ensure products or assignments align with the companies.
Essential Functions:
  • Carries out inspection activities to ensure the quality of products and raw materials used in the production of products to meet customer or internal standards
  • Responsible for the correct handling of the corresponding fixtures and equipment
  • Correct use of quality inspection records following GMP requirements
  • Ensures the consistency and quality of records by editing and proofreading all documentation prior to handling it to the documentation center for storage
  • Maintains and archives documents in an organized and retrievable state (manual or electronic) for compliance to procedures, regulations and standards
  • Safekeeping all quality records of In-Process Inspection
  • Schedules periodic document reviews to ensure documents are compliant with Globus requirements and processes as well as external regulations
  • Communicates corrections and improvement opportunities
  • Ensures timely release of subassemblies and assemblies by executing, reviewing and approving Device History Records (DHRs) and ERP transactions per internal requirements
  • Responsible for the control of nonconforming material (identification, segregation)
  • Interfaces with cross functional team to ensure internal and external compliance requirements are followed and implemented per requirements
  • Labels and segregates components and assemblies
  • Notifies cross functional departments including Production, Quality and Purchasing on component/assembly dispositions and/or material holds
  • Manages component/assembly disposition and queries using the QAD system
  • Supports with External Audits activities when required and as directed
  • Responsible for the release of subassemblies, assemblies and final assemblies
  • Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies
  • Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
  • Represents the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Qualifications:
  • Quality Inspector or advanced studies in relevant technical discipline required
  • No fewer than three (3) years of directly related experience, having experience in a class II or III medical device environment quality inspection is preferred, complaints lab inspection or receiving inspection is also preferred, inspection small components using a microscope is preferred
  • Experience in the medical device industry and with knowledge performing their function within the Food & Drug Administration (FDA), Quality System Regulations (QSRs), International Organization of Standardization (ISO 13485) is preferred
  • Experience with QAD preferred
  • Prior experience working with US companies is a plus
  • IPC-A-610 certification or knowledge in medical device component welding through resistance welding, spot welding or laser welding is a plus
  • Handling of electrical components is a plus
  • Experience with ESD processes is a plus
  • Ability to read and interpret documents such as job travelers, plans, sketches, diagrams and other procedural materials and documents
  • Fundamental geometry, fractions, percents, relationships and measurements
  • Ability to work independently with little supervision, as well as in "team" work
  • Effective interpersonal skills and dexterity on the job with a culturally diverse employee population
  • Knowledge of measurement instruments, sample plans is a plus
  • Experience with inspecting small parts under magnification is a plus

  • Work environment and physical requirements:
    • Production area / clean room
    • Some exposure to noisy equipment
  • Strong organizational and follow-up skills
  • Excellent verbal and written communication skills
  • Attention to detail
  • Self-starter
  • Advanced critical thinking and problems-solving skills
  • Proficiency in using Microsoft Office products

Physical Demands:
The physical demands listed here are representative of those that must be met by and employee to successfully perform the essential functions of this job.
  • Required to sit; climb or balance; and stoop, kneel, crouch or crawl
  • Required to regularly lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds
  • Required to possess specific visons abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus.

Our Values:
Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven.
  • Passionate about Innovation: Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate in our role in improving the lives of patients by continuously developing better solutions.
  • Customer Focused: We listen to our customers' needs and respond with a sense of urgency.
  • Teamwork: Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger.
  • Driven: We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.

Equal Employment Opportunity:
Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees' talents and support an environment that is inclusive and respectful.
Other Duties:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

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