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Fda Inspector Jobs in Oregon (NOW HIRING)

Quality Engineer 2

Hillsboro, OR · On-site

$85 - $120/hr

This role drives quality objectives during product development, ensuring compliance with FDA ... Develop and maintain final inspection plans; support validation of inspection methods. * Coordinate ...

New

Acts as contact and liaison for inspections and audits including customer, FDA, ODA, Kosher, and Halal. * Performs internal audits and follows up on action items to ensure their closure.

New

Delivery Driver - Medical Equipment

Salem, OR

$17.25 - $21.25/hr

Inspect and maintain company-provided delivery vehicle, ensuring safety during the loading and ... Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA ...

Delivery Driver - Medical Equipment

Portland, OR · On-site

$18 - $22/hr

Inspect and maintain company-provided delivery vehicle, ensuring safety during the loading and ... Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA ...

Food Safety & Quality Assurance Manager

Portland, OR · On-site

$82K - $103K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Proven experience leading regulatory, customer, and third-party audits and inspections. * Strong knowledge of FDA and USDA regulations, FSMA Preventive Controls, HACCP principles, and current Good ...

Food Safety & Quality Assurance Manager

Portland, OR · On-site

$82K - $103K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Proven experience leading regulatory, customer, and third-party audits and inspections. * Strong knowledge of FDA and USDA regulations, FSMA Preventive Controls, HACCP principles, and current Good ...

Food Safety & Quality Assurance Manager

Beaverton, OR · On-site

$82K - $103K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Proven experience leading regulatory, customer, and third-party audits and inspections. * Strong knowledge of FDA and USDA regulations, FSMA Preventive Controls, HACCP principles, and current Good ...

Food Safety & Quality Assurance Manager

Beaverton, OR · On-site

$82K - $103K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Proven experience leading regulatory, customer, and third-party audits and inspections. * Strong knowledge of FDA and USDA regulations, FSMA Preventive Controls, HACCP principles, and current Good ...

Showing results 41-60

Fda Inspector information

See Oregon salary details

$25.9K

$58.1K

$104.7K

How much do fda inspector jobs pay per year?

As of Aug 20, 2026, the average yearly pay for fda inspector in Oregon is $58,086.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,700.00 and $67,100.00 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 popular job titles related to Fda Inspector jobs in Oregon?

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

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

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

What cities in Oregon are hiring for Fda Inspector jobs?

Cities in Oregon with the most Fda Inspector job openings:

Infographic showing various Fda Inspector job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, 2% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $58,086 per year, or $27.9 per hour.

Associate Director of Quality Assurance, Operations

Serán BioScience

Bend, OR • On-site

$150 - $190/hr

Other

Re-posted 10 days ago


Job description

Serán is seeking a QA Associate Director, who oversees the day‑to‑day operations of the Quality Assurance department with oversight of clinical manufacturing and warehouse activities in addition to disposition of raw materials and drug products. Required attributes include a results‑driven and broad‑minded quality assurance professional with extensive experience in compliance and regulations, quality systems management, investigations, training and mentoring, client relations, performance management, and change management. Extensive experience with direct or quality oversight of manufacturing operations is required.

The successful candidate will have excellent problem‑solving skills and will identify critical quality objectives, develop cross‑functional, collaborative, and creative teams, and improve, adapt, and execute practical solutions in competitive and fast‑paced environments.

Supervisory Responsibilities
  • Leads and mentors Quality Assurance personnel.
  • Recruits, interviews,hiresand trains new staff.
  • Oversees daily workflow of the department.
Responsibilities
  • Leads and implements continuous improvement initiatives to reduce risk and improve efficiency for the company’s quality systems and department operations
  • Management and scheduling of department operations
  • Oversees and conducts review and approval of Investigations, CAPAs, Complaints, and Change Management
  • Review and approval of SOPs, batch records, raw material records, and certificates of conformance/compliance
  • Responsible for Quality oversight of activities involving raw material, drug product manufacturing, packaging, labeling, and warehouse activities
  • Assures cGMP compliance systems and processes are in place to support raw material and drug product review, release, storage, and shipping
  • Defines and maintains a strong people management, training, and engagement culture to ensure a high and constantly improving right first‑time rate
  • Supports internal audits, client audits and regulatory inspections
Required Skills and Experience
  • Expert knowledge of GMP guidelines and Quality expectations for preclinical and clinical phase manufacturing operations
  • In-depth understanding and application of cGMP principles, concepts, practices, and standards
  • Experience with regulatory inspections by the FDA and EU authorities
  • Ability to influence diverse stakeholders and drive accountability and decision‑makingcrossfunctionally
  • Demonstrated ability to partner with other functional groups to achieve business objectives
  • Experience organizing and managing group responsibilities while working independently with minimal oversight
  • Time and project management skills with the ability to multi‑task and meet deadlines
  • Excellent verbal and written communication skills
  • Communicateseffectively andmaintainsproductive relationships with coworkers, clients, and other contacts outside of the company
  • Excellent organizational skills and attention to detail
  • Strong analytical and problem‑solving skills
  • Strong supervisory and leadership skills
Education and Experience
  • Minimum of a bachelor’s degree, preferably in a scientific discipline. An advanced degree is preferred
  • 10+ years previous GMP and Quality experience in the Pharmaceutical industry with quality oversite of Oral Solid Dose manufacturing
  • Experience with regulatory inspections by the FDA and EU authorities
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