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Fda Contract Jobs in Rhode Island (NOW HIRING)

Bradford Soap Works Inc

Quality Engineer

West Warwick, RI · On-site

$69K - $90K/yr

The Quality Engineer supports quality systems and product quality for a personal care contract ... Support and maintain site quality systems in compliance with regulatory (ISO, GMP, FDA, etc.) and ...

Bradford Soap Works Inc

Quality Engineer

West Warwick, RI · On-site

$69K - $90K/yr

The Quality Engineer supports quality systems and product quality for a personal care contract ... Support and maintain site quality systems in compliance with regulatory (ISO, GMP, FDA, etc.) and ...

GreenKiss Staffing Solutions, Inc.

Be Seen First

Blending Operator (Food)

Warren, RI · On-site

$19 - $20/hr

Experience with food safety regulations (FDA/USDA standards) * Familiarity with industrial mixing ... contract, contract-to-hire, on-site managed services, and direct professional placements. We ...

Actalent

Senior Software Engineer

Providence, RI · Hybrid

$50 - $70/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Produce and maintain clear, comprehensive documentation in alignment with FDA software design ... Job Type & Location This is a Contract position based out of Providence, RI. Pay and Benefits The ...

Blount Fine Foods

Corporate Counsel

Warren, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Advise business and functional leaders on contracts, compliance, risk management, employment law ... Manage regulatory matters for a wide variety of issues (EPA, DEM, FDA, USDA, etc.) Manage outside ...

Pharmaron

Senior Scientist I, QC

Coventry, RI · On-site

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Coventry, RI About Pharmaron Pharmaron is a global contract research and manufacturing organization ... Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance * Evidence of ability to ...

Pharmaron

Scientist II, Analytical Chemistry

Coventry, RI · On-site

$75K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Coventry, RI About Pharmaron Pharmaron is a global contract research and manufacturing organization ... Working knowledge of cGMP and applicable FDA, EMA and ICH guidance * Excellent communication skills ...

Pharmaron

Senior Scientist I, QC

Coventry, RI · On-site

$100K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Coventry, RI About Pharmaron Pharmaron is a global contract research and manufacturing organization ... Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance * Evidence of ability to ...

Pharmaron

Maintenance Technician

Coventry, RI · On-site

$35 - $50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Coventry, RI - Onsite Hourly Rate: $35-$50 per hour About Pharmaron Pharmaron is a global contract ... Prior experience in a highly regulated environment such as FDA, DEA, NRC or similarly regulated ...

Pharmaron

Maintenance Technician

Coventry, RI · On-site

$35 - $50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Coventry, RI - Onsite Hourly Rate: $35-$50 per hour About Pharmaron Pharmaron is a global contract ... Prior experience in a highly regulated environment such as FDA, DEA, NRC or similarly regulated ...

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Showing results 1-20

All JobsFda Contract JobsFda Contract Jobs in Rhode Island

Fda Contract information

See Rhode Island salary details

$40.2K

$103.8K

$136.1K

How much do fda contract jobs pay per year?

As of Aug 13, 2026, the average yearly pay for fda contract in Rhode Island is $103,840.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,200.00 and $116,500.00 per year, depending on experience, location, and employer.

What is an Fda contract?

An FDA Contract job refers to a temporary or project-based position working with or for the U.S. Food and Drug Administration (FDA) through a contractual agreement. These roles can be with the FDA directly or through third-party contractors supporting FDA initiatives. Responsibilities may include regulatory compliance, data analysis, scientific research, IT support, or administrative tasks. Contract positions vary in duration and benefits but provide opportunities to work in a highly regulated environment.

What are the primary responsibilities of someone working under an Fda contract?

As an FDA Contract professional, your primary responsibilities usually include developing, reviewing, and managing documents and agreements in accordance with FDA guidelines and regulations. You may coordinate closely with regulatory affairs, legal, and project management teams to ensure that all contract terms support compliance and meet project timelines. Daily tasks might involve drafting and negotiating contract language, tracking deliverables, and supporting regulatory submissions. This role is both detail-oriented and collaborative, and it provides valuable experience for those seeking advancement into regulatory management or specialist positions.

What are the key skills and qualifications needed to thrive in the Fda contract position, and why are they important?

To thrive in an FDA Contract role, you need strong knowledge of FDA regulations, compliance processes, and contract management, often supported by a background in life sciences or regulatory affairs. Familiarity with tools such as Document Control Systems, eCTD publishing software, and experience with regulatory submission platforms are typically required. Outstanding attention to detail, negotiation skills, and the ability to collaborate across cross-functional teams help candidates excel. These competencies are critical for ensuring contracts meet strict regulatory standards and for navigating the complexities of FDA approval and compliance procedures.

What are the most commonly searched types of Fda jobs in Rhode Island?

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

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

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

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

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

What cities in Rhode Island are hiring for Fda Contract jobs?

Cities in Rhode Island with the most Fda Contract job openings:

Fda Contract jobs near you
Infographic showing various Fda Contract job openings in Rhode Island as of August 2026, with employment types broken down into 79% Full Time, 15% Part Time, 5% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $103,840 per year, or $49.9 per hour.

Quality Engineer

Bradford Soap Works Inc

West Warwick, RI • On-site

$69K - $90K/yr

Full-time

Re-posted 12 days ago

Job description

Job Title: Quality Engineer

Reports to: Quality Operations Manager

Job Function:

The Quality Engineer supports quality systems and product quality for a personal care contract manufacturing operation. This role has no direct reports and works cross‑functionally with Operations, Engineering, R&D, and Customer Service to ensure compliance with customer, regulatory (ISO, FDA, Organic, etc.), and internal requirements. The Quality Engineer plays a key role in audits, root cause analysis, and customer complaint management while driving continuous improvement across the site.

Essential Duties and Responsibilities:

Quality Systems and Compliance

  • Support and maintain site quality systems in compliance with regulatory (ISO, GMP, FDA, etc.) and applicable customer requirements.
  • Lead internal audits, customer audits, and third‑party audits; prepare documentation, support on‑site activities, and ensure timely closure of audit findings.
  • Assist with document control, SOP updates, and change management activities.
  • Support risk assessments, control plans, and quality metrics reporting.

Root Cause Analysis & Corrective Actions

  • Lead and facilitate root cause analysis using structured problem‑solving tools (e.g., 5 Whys, Fishbone, FMEA).
  • Develop, implement, and track corrective and preventive actions (CAPAs) to ensure effectiveness and sustainability.
  • Partner with Operations and Engineering to address quality issues, reduce defects, and improve process capability

Customer Complaint Management

  • Manage customer complaints from receipt through closure, including investigation, root cause analysis, corrective action development and implementation, and response preparation.
  • Coordinate cross‑functional investigations to ensure timely, accurate, and professional customer responses.
  • Identify complaint trends and drive systemic improvements to prevent recurrence.

Manufacturing & Process Support

  • Provide quality support to manufacturing operations, including deviation investigations and nonconformance management.
  • Support sampling, documentation, and shipment of raw materials, batch, and finished product samples to outside labs for testing.
  • Support new product introductions (NPI), validation protocols (IQ/OQ/PQ), and process changes and subsequent process change control from a quality perspective.
  • Review batch records, inspection data, and quality documentation as needed.

Continuous Improvement

  • Analyze quality data to identify trends, risks, and improvement opportunities.
  • Participate in Lean, Six Sigma, or other continuous improvement initiatives.
  • Promote a culture of quality, compliance, and accountability throughout the organization.

Minimum Knowledge, Skills and Abilities:

  • Bachelor’s degree in Engineering, Quality, Chemistry, or a related technical field.
  • 3+ years of quality engineering or quality assurance experience in a manufacturing environment.
  • Experience with audits, nonconformance investigations, customer complaint management, root cause analysis, CAPA development and implementation.
  • Working knowledge of GMP and quality management systems.
  • Strong analytical, organizational, and problem‑solving skills.
  • Effective written and verbal communication skills.
  • Preference for Lean, Six Sigma or quality certification.
  • Familiarity with regulatory compliance requirements applicable to certifications such as organic, Halal, naturals etc… would be desirable.

Physical & Work Environment:

  • Manufacturing environment with regular presence on the production floor.
  • Ability to sit, stand, walk, and occasionally lift up to 25 lbs.
  • Occasional travel for customer or supplier audits may be required.

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