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Fda Inspector Jobs in Rhode Island (NOW HIRING)

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How much do fda inspector jobs pay per year?

As of Aug 22, 2026, the average yearly pay for fda inspector in Rhode Island is $53,802.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,700.00 and $62,200.00 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 Rhode Island?

The most popular types of Fda Inspector jobs in Rhode Island are:

What are popular job titles related to Fda Inspector jobs in Rhode Island?

For Fda Inspector jobs in Rhode Island, the most frequently searched job titles are:

What job categories do people searching Fda Inspector jobs in Rhode Island look for?

The top searched job categories for Fda Inspector jobs in Rhode Island are:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $53,802 per year, or $25.9 per hour.

Senior Scientist, Analytical Chemistry

Pharmaron

Coventry, RI • On-site

$90K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 days ago

Job description

Position: Senior Scientist, Analytical Chemistry
Salary Range: $90k - $130k
Location: Coventry, RI
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
Job Overview
The Senior Scientist - Analytical Chemistry will serve as a key technical resource within the Quality Control laboratory supporting API manufacturing and development programs at Pharmaron's Coventry, RI facility.
This role is responsible for supporting analytical method validation, transfer, troubleshooting, and QC testing of raw materials, intermediates, and active pharmaceutical ingredients in a cGMP-regulated laboratory environment. The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations.
Key Responsibilities
  • Support analytical method validation, verification, and transfer activities within the QC laboratory.
  • Troubleshoot complex analytical challenges related to API characterization and GMP testing.
  • Review analytical data, laboratory notebooks, and instrument qualification documentation to ensure scientific accuracy and regulatory compliance.
  • Lead or support laboratory investigations, deviations, and root cause analyses.
  • Maintain laboratory equipment and serve as system owner for analytical instrumentation, including qualification and maintenance activities.
  • Provide technical mentorship and scientific guidance to QC scientists and laboratory personnel.
  • Prepare and revise standard operating procedures (SOPs), analytical methods, and technical documentation.
  • Support internal and external regulatory inspections and client audits as an analytical subject matter expert.
  • Collaborate with cross-functional teams including Manufacturing, Process Chemistry, Quality Assurance, and Regulatory Affairs.
  • Contribute to continuous improvement initiatives that enhance QC laboratory efficiency and analytical capabilities.
  • Perform other related assignments and duties, as required and assigned.

What We're Looking For
  • Ph.D. in Chemistry or a related field with 1-4 years of postdoctoral or industry experience.
  • MS with 5-8 years of pharmaceutical industry experience, BS with 7-10 years of relevant pharmaceutical industry experience
  • 3 years of experience (may include Ph.D. experience) with core analytical instrumentation such as HPLC, GC, FTIR, UV, Mass Spectrometry.
  • Demonstrated experience applying analytical techniques to solve complex scientific problems related to method validation, troubleshooting, and implementation
  • Strong hands-on expertise with analytical instrumentation including:
    • HPLC / UPLC
    • GC
    • FTIR
    • UV
    • Mass Spectrometry
  • Experience supporting API manufacturing or pharmaceutical QC laboratories
  • Proven ability to troubleshoot analytical instrumentation and laboratory methods
  • Working knowledge of cGLP / cGMP and applicable FDA, EMA, and ICH regulatory guidelines
  • Experience contributing to multidisciplinary scientific teams and cross-functional projects
  • Experience mentoring or supervising laboratory personnel preferred
  • Strong analytical thinking, scientific judgment, and problem-solving skills
  • Excellent written and verbal communication skills

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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