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Fda Inspector Jobs in New York (NOW HIRING)

MTF Biologics

Manager, Regulatory Affairs

Edison, NJ · On-site +1

$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

MTF Biologics

Manager, Regulatory Affairs

Edison, NJ · On-site +1

$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

Amneal Pharmaceuticals

REMS Manager

Bridgewater, NJ

Support FDA inspections and internal audits. Track commitments, findings, CAPAs, and remediation activities. Ensure all required REMS documentation is current and inspection-ready. * Vendor and ...

Amneal Pharmaceuticals

REMS Manager

Bridgewater, NJ

Support FDA inspections and internal audits. Track commitments, findings, CAPAs, and remediation activities. Ensure all required REMS documentation is current and inspection-ready. * Vendor and ...

Amneal Pharmaceuticals

REMS Manager

Bridgewater, NJ

Support FDA inspections and internal audits. Track commitments, findings, CAPAs, and remediation activities. Ensure all required REMS documentation is current and inspection-ready. * Vendor and ...

Amneal Pharmaceuticals

REMS Manager

Bridgewater, NJ · On-site

$140K - $155K/yr

Support FDA inspections and internal audits. Track commitments, findings, CAPAs, and remediation activities. Ensure all required REMS documentation is current and inspection-ready. * Vendor and ...

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Showing results 21-40

All JobsFda Inspector JobsFda Inspector Jobs in New York

Fda Inspector information

See New York salary details

$26.8K

$60.1K

$108.3K

How much do fda inspector jobs pay per year?

As of Sep 5, 2026, the average yearly pay for fda inspector in New York is $60,105.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,100.00 and $69,500.00 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 the most commonly searched types of Fda Inspector jobs in New York?

The most popular types of Fda Inspector jobs in New York are:

What are popular job titles related to Fda Inspector jobs in New York?

For Fda Inspector jobs in New York, the most frequently searched job titles are:

What job categories do people searching Fda Inspector jobs in New York look for?

The top searched job categories for Fda Inspector jobs in New York are:

What cities in New York are hiring for Fda Inspector jobs?

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Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in New York as of August 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 78% In-person, and 22% Remote job distribution, with an average salary of $60,105 per year, or $28.9 per hour.

Manager, Regulatory Affairs

MTF Biologics

Edison, NJ • On-site, Remote

$125K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 28 days ago

MTF Biologics rating

9.2

Company rating: 9.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

Job description

Overview
Responsible for the day-to-day leadership and operational management of the Regulatory Affairs function. This role oversees Regulatory Affairs personnel and ensures effective execution of U.S. and international regulatory activities, including regulatory submissions, inspections and audits, recalls, licensing, labeling and promotional review, quality system documentation, risk management, and design control support. Ability to travel up to 20% of time to MTF locations and to suppliers as required
Monday through Friday 8:15am to 4:30pm
Salary Range : $125,000/yr.
Responsibilities
  • Lead, coach, and develop Regulatory Affairs staff, including staffing plans, performance management, training, and competency maintenance. Also performs active management and observations of staff for compliance with regulations and process efficiencies.
  • Assist in managing the budget for Regulatory Affairs department, including salaries, benefits, external vendors/consultants, supplies, services and internal expenses. Responsible for formulating/submitting budgets and managing to expense within budget requirements. Tracks monthly "budget to actual" performance.
  • Oversee and assist in the preparation, submission, and maintenance of U.S. and international regulatory filings (FDA, CE Marking, Canada, Australia, and other global markets).
  • Ensure maintenance of all applicable licenses, accreditations (AATB), and ISO 9001 / 13485 certifications.
  • Participates in the development of regulatory strategies and pathway to support the regulatory designation of new products and tissues.
  • Serve as a primary regulatory contact during inspections and audits and lead regulatory intelligence activities.
  • Communicates and coordinates with VP and MTF senior management and other department heads on regulatory issues and regulatory strategies which may impact MTF's ability to fulfill its mission.
  • Communicates with federal/state regulatory agencies, international government and notified bodies, and AATB related to applicable new or revised regulations and standards
  • Assist on special projects and performs additional duties as assigned.

Qualifications
  • Bachelor's degree in a scientific or related field, or a combination of education and equivalent work experience
  • 7+ Years of overall experience
  • 5 Years of Managerial experience
  • 5 Years or Human tissue or medical device manufacturing
  • Thorough understanding of FDA, QSR, cGMP, ISO regulations for medical devices, diagnostics or pharma Must exhibit people management, effective communication skills
  • Attention to detail, critical thinking, problem-solving, and organizational skills
  • 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
  • Ability to travel up to 20% of time to MTF locations and to suppliers as required

Benefits Information
At MTF Biologics we provide comprehensive benefits and resources to support our employees physical, emotional, and financial health.
  • 4 weeks Paid Time Off (PTO)
  • Paid Holidays
  • Medical, Dental, Vision Insurance and Prescription Drug Insurance
  • 401K plan with company match
  • Short & Long Term Disability
  • Life & Accidental Death Insurance
  • Tuition Reimbursement
  • Health Care/Dependent Care Flexible Spending Accounts
  • Adoption Assistance
  • Voluntary Benefits (e.g., Pet Insurance, Legal, home and auto insurance)
  • Sword Health (at home Physical Therapy)

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