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Fda Inspector Jobs in Queens, NY (NOW HIRING)

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Senior FDA Regulatory Attorney

New York, NY · Remote

$250K - $350K/yr

Counsel clients regarding FDA regulations, guidance, inspections, investigations, warning letters, and enforcement actions. * Provide guidance on: * * Compounding (503A and 503B) * Drug Supply Chain ...

Quality Inspector A large labeling company is looking for Quality Inspectors. The labeling company ... Requirements: 1 - 2 years' experience in related field Knowledge of FDA/cGMP guidelines Basic ...

Quality Operations Manager

Ridgefield, NJ · On-site

$125K - $155K/yr

Serve as the site quality leader during FDA and customer inspections; ensure continuous inspection readiness * Drive resolution of compliance issues and manage CAPAs effectively * Collaborate cross ...

... Maintain FDA inspection-ready documentation packages • Collaborate with QA leadership to define validation roadmap and system requirements • Manage defect tracking with CAPA processes for ...

Lead and support FDA inspections, customer audits, and third-party audits; ensure timely completion of corrective actions. * Provide QA oversight for manufacturing, packaging, labeling, warehousing ...

And let's not forget the sanitation standards that would pass an FDA inspection, but not without a lot of eye rolls and sighs from the staff who just want to breathe.

Manager, Regulatory Affairs

Edison, NJ · On-site +1

$99K - $125K/yr

Prior experience handling FDA inspections for medical devices, diagnostics, biologics and/or pharma Demonstrated success in obtaining US FDA regulatory clearance/approval for medical technologies

Job Title: QA Inspector I (Warehouse) Location: 7 Oser Avenue, Hauppauge, NY (Onsite) Employment ... Ensure that the artwork complies with all relevant regulatory guidelines (e.g., FDA, EMA) and ...

Job Title: QA Inspector I (Warehouse) Location: 7 Oser Avenue, Hauppauge, NY (Onsite) Employment ... Ensure that the artwork complies with all relevant regulatory guidelines (e.g., FDA, EMA) and ...

Manager, Regulatory Affairs

Edison, NJ · On-site +1

$99K - $125K/yr

Prior experience handling FDA inspections for medical devices, diagnostics, biologics and/or pharma Demonstrated success in obtaining US FDA regulatory clearance/approval for medical technologies

Manager, Regulatory Affairs

Edison, NJ · On-site +1

$99K - $125K/yr

Prior experience handling FDA inspections for medical devices, diagnostics, biologics and/or pharma Demonstrated success in obtaining US FDA regulatory clearance/approval for medical technologies

S. FDA inspections and direct support for EU Notified Body audits and ROW competent authority inspections. Organizational Leadership & Regulatory Excellence * Mentor and develop regulatory team ...

S. FDA inspections and direct support for EU Notified Body audits and ROW competent authority inspections. Organizational Leadership & Regulatory Excellence * Mentor and develop regulatory team ...

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Fda Inspector information

See Queens, NY salary details

$25.6K

$57.3K

$103.3K

How much do fda inspector jobs pay per year?

As of Jul 27, 2026, the average yearly pay for fda inspector in Queens, NY is $57,327.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,200.00 and $66,300.00 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 Queens, NY? For Fda Inspector jobs in Queens, NY, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Queens, NY look for? The top searched job categories for Fda Inspector jobs in Queens, NY are:
What cities near Queens, NY are hiring for Fda Inspector jobs? Cities near Queens, NY with the most Fda Inspector job openings:
Infographic showing various Fda Inspector job openings in Queens, NY as of July 2026, with employment types broken down into 100% Full Time. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $57,327 per year, or $27.6 per hour.
Senior FDA Regulatory Attorney

Senior FDA Regulatory Attorney

The Rockridge Group

New York, NY • Remote

$250K - $350K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

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Job description

TITLE: FDA REGULATORY ATTORNEY

Firm X is seeking an experienced FDA Regulatory Attorney to join its growing FDA and Life Sciences practice. Due to significant client demand and a steady influx of new FDA-related matters, we are looking for an attorney with deep regulatory experience advising pharmaceutical, compounding, medical device, biotechnology, healthcare, and related life sciences clients.

Key Responsibilities:

  • Advise clients on FDA regulatory compliance matters involving drugs, biologics, medical devices, dietary supplements, and compounding pharmacies.
  • Counsel clients regarding FDA regulations, guidance, inspections, investigations, warning letters, and enforcement actions.
  • Provide guidance on:
    • Compounding (503A and 503B)
    • Drug Supply Chain Security Act (DSCSA)
    • cGMP compliance
    • Drug and device manufacturing requirements
    • FDA registrations and annual filings
    • Labeling, marketing, and advertising reviews
    • Product recalls and withdrawals
    • Import/export compliance
    • Veterinary medicine and veterinary compounding
  • Assist with NDA, ANDA, 510(k), PMA, OTC, and other FDA submissions.
  • Advise clients regarding clinical trial compliance, research agreements, informed consent forms, IRB requirements, and related regulatory matters.
  • Review scientific and clinical literature to support regulatory strategies and client guidance.

Qualifications:

  • J.D. from an accredited law school.
  • Licensed and in good standing in at least one U.S. jurisdiction.
  • 10+ years of FDA regulatory experience.
  • Prior law firm experience strongly preferred; exceptional in-house FDA counsel will also be considered.
  • Strong working knowledge of pharmaceutical, medical device, compounding, and healthcare regulatory frameworks.
  • Experience with FDA inspections, 483 responses, warning letters, and compliance programs preferred.
  • Clinical trial experience is a plus.
  • Patent and/or copyright filing experience is a plus.
  • Excellent drafting, analytical, and client counseling skills.

Company Description

About The Rockridge Group:
TRG is a privately held Limited Liability Company committed to connecting businesses with job seekers. We deliver high quality contingent personnel to our clients using our 3-step collaborative engagement model:
Collaborate. We partner with you to understand the unique needs of your business before we propose a solution.
Strategize. Based on your goals and staffing challenges, we develop high impact solutions designed for your industry.
Engage. We work with your team before, during, and after every engagement to deliver 100% satisfaction.
With over ten (10) years experience in the resource solutions sector, principals Greg Donner [link to bio] and Ronald Lom [link to bio] leverage the power of strategic partnership to create a powerful staffing model that improves your quality of hire.