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Fda Inspector Jobs in Schenectady, NY (NOW HIRING)

AMRI

Senior Quality Assurance Specialist

Rensselaer, NY

$103K - $129K/yr

... g., FDA, ICH). * Knowledge of pharmaceutical processes. * USFDA inspection experiences (participating or leading) * Excellent communication and organizational skills, as well as negotiation ...

AMRI

Quality Assurance Specialist II

Rensselaer, NY

May perform QA visual inspection activities when required * Participate in regulatory and client ... cGMP FDA-regulated industry * OR MA/MS Degree in Chemistry or a relevant field and 1 year of ...

AMRI

Quality Assurance Specialist II

Rensselaer, NY

May perform QA visual inspection activities when required * Participate in regulatory and client ... cGMP FDA-regulated industry * OR MA/MS Degree in Chemistry or a relevant field and 1 year of ...

Stewart's Shops

Dairy Sanitation

Saratoga Springs, NY · On-site

$24/hr

... equipment for inspection and hand cleaning, then setting up for next day's production run ... Carry out tasks in accordance with Stewart's policies, OSHA regulations, and USDA and FDA ...

AMRI

Manager, QC Lab Remediation

Rensselaer, NY

Play a key role in QC lab inspection readiness plan * Perform gap assessments for Curia network ... Expert in cGMP, USP, EP and FDA regulations * Technical competence including the understanding of ...

Curia, Inc.

Manager, QC Lab Remediation

Rensselaer, NY · On-site

Play a key role in QC lab inspection readiness plan * Perform gap assessments for Curia network ... Expert in cGMP, USP, EP and FDA regulations * Technical competence including the understanding of ...

Stewart's Shops

Dairy Sanitation

Saratoga Springs, NY · On-site

$24/hr

... inspection and hand cleaning, then setting up for next day's production run. • Operation of ... USDA and FDA regulations. • Take direction from Sanitation Supervisor to resolve sanitation ...

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All JobsFda Inspector JobsFda Inspector Jobs in Schenectady, NY

Fda Inspector information

See Schenectady, NY salary details

$23.7K

$53.2K

$95.8K

How much do fda inspector jobs pay per year?

As of Jul 28, 2026, the average yearly pay for fda inspector in Schenectady, NY is $53,155.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,200.00 and $61,400.00 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 Schenectady, NY? For Fda Inspector jobs in Schenectady, NY, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Schenectady, NY look for? The top searched job categories for Fda Inspector jobs in Schenectady, NY are:
What cities near Schenectady, NY are hiring for Fda Inspector jobs? Cities near Schenectady, NY with the most Fda Inspector job openings:
Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Schenectady, NY as of July 2026, with employment types broken down into 84% Full Time, 13% Part Time, 2% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $53,155 per year, or $25.6 per hour.
Senior Manager, IT Applications - Laboratory Informatics

Senior Manager, IT Applications - Laboratory Informatics

Regeneron Pharmaceuticals, Inc.

Troy, NY • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago

Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Applications Manager (Manager or Senior Manager) to join our IOPS IT team, overseeing the day-to-day maintenance, support, and development of Regeneron's IT Applications portfolio - including Empower CDS, SDMS, and other business-critical systems. In this role, you will lead a team of analysts, drive audit readiness and compliance, and ensure applications are maintained in a validated and compliant state - while collaborating closely with peer managers, QA, IT leadership, and global counterparts. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where:
  • Location: Troy, New York, United States
  • Work model: Monday - Friday 8am - 4:30pm

Discover your role:
  • Lead and develop a team of IT Applications analysts through performance management, coaching, mentoring, and goal setting; conduct monthly performance reviews and annual evaluations
  • Drive audit readiness across the application portfolio; serve as a key point of contact during FDA inspections and internal audits, ensuring systems, audit trails, and documentation are inspection-ready at all times
  • Ensure all supported applications are maintained in a compliant and validated state; proactively identify and resolve data integrity and compliance issues in accordance with 21 CFR Part 11, ALCOA+ principles, applicable SOPs, and policies
  • Maintain accuracy of system documentation including User Requirement Specifications, Design Specifications, Configuration Specifications, and Test Plans for validated systems
  • Collaborate closely with peer managers overseeing complementary application portfolios to ensure alignment, shared best practices, and coordinated delivery across the broader IOPS IT Applications function
  • Partner with global counterparts to support and maintain globally deployed QC systems in a consistent and compliant manner
  • Manage vendor relationships including performance, contract adherence, and delivery of services in line with business and regulatory compliance requirements
  • Develop and implement operational metrics and controls; drive continuous improvement initiatives that enhance workflows, system reliability, and team efficiency; contribute to the strategic vision of the IOPS IT Applications function
  • Strong knowledge of cGMP, GAMP, 21 CFR Part 11, and Annex 11; experience supporting applications in a highly regulated GMP laboratory or IT environment preferred
  • Demonstrated understanding of ALCOA+ principles and data integrity requirements in biopharmaceutical production
  • Proven ability to lead teams through FDA inspections and internal audits with confidence and thoroughness
  • Knowledge of Regulatory Asset Manager systems advantageous

This role requires:
  • Bachelor's degree in Information Technology, Science, Engineering, Computer Science, or a related field
  • Manager: 7+ years of relevant experience with 3+ years managing teams
  • Senior Manager: 8+ years of relevant experience with 4+ years managing teams
  • May consider experience in lieu of education. Level is determined based on qualifications relevant to the role

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$108,000.00 - $206,100.00

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