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Fda Inspector Jobs in Denver, CO (NOW HIRING)

Biointellisense

Operations Technician

Golden, CO

$25 - $27/hr

Other duties and special projects as assigned Job Requirements * 2-3 years of manufacturing and inspection experience within the medical device industry preferred * Previous experience in an FDA and ...

Lincare

Delivery Driver - Medical Equipment

Frederick, CO · On-site

$15.16 - $23/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 ...

Lincare

Delivery Driver - Medical Equipment

Denver, CO · On-site

$19.29 - $23/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 ...

Accurate Personnel LLC

QC Manager

Brighton, CO

$61K - $64K/yr

  • Medical

  • Dental

  • Vision

Review, follow up and file distribution public health inspection reports * Have cheese inventory ... Maintain FDA vendor tracking sheet and send to FDA compliance team quarterly * Assist with Quality ...

VPI Compounding

Quality Control -- Microbiology

Centennial, CO · On-site

$26 - $31/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Ensure alignment with USP chapters, FDA guidance, and internal procedures * Support regular SOP ... Support regulatory inspections with required documentation * Maintain an audit-ready state through ...

Eurofins Scientific

Quality Control Specialist

Centennial, CO

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Maintain accurate and complete records in accordance with regulatory guidelines (e.g., CLIA, FDA 21 CFR Part 11, ISO 15189). * Participates in quality audits or regulatory inspections. * Assist with ...

Eurofins

Quality Control Specialist

Centennial, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Maintain accurate and complete records in accordance with regulatory guidelines (e.g., CLIA, FDA 21 CFR Part 11, ISO 15189). * Participates in quality audits or regulatory inspections. * Assist with ...

Medtronic

Prin Quality Engineer

Lafayette, CO · On-site

$75K - $96K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... FDA Part 820), and other international standards, and participate in regulatory audits and inspections. * Oversee design validation and design verification activities of user needs and design inputs ...

New

Medtronic

Prin Quality Engineer

Lafayette, CO · On-site

$75K - $96K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... FDA Part 820), and other international standards, and participate in regulatory audits and inspections. * Oversee design validation and design verification activities of user needs and design inputs ...

New

Medtronic

Prin Quality Engineer

Lafayette, CO · On-site

$75K - $96K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... FDA Part 820), and other international standards, and participate in regulatory audits and inspections. * Oversee design validation and design verification activities of user needs and design inputs ...

New

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Showing results 21-40

All JobsFda Inspector JobsFda Inspector Jobs in Denver, CO

Fda Inspector information

See Denver, CO salary details

$25.2K

$56.5K

$101.9K

How much do fda inspector jobs pay per year?

As of Aug 16, 2026, the average yearly pay for fda inspector in Denver, CO is $56,548.00, according to ZipRecruiter salary data. Most workers in this role earn between $39,600.00 and $65,400.00 per year, depending on experience, location, and employer.

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.

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.

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 the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

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 Denver, CO?

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

What job categories do people searching Fda Inspector jobs in Denver, CO look for?

The top searched job categories for Fda Inspector jobs in Denver, CO are:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Denver, CO as of August 2026, with employment types broken down into 73% Full Time, 14% Part Time, 1% Temporary, 11% Contract, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $56,548 per year, or $27.2 per hour.

Senior Pharmaceutical CQV Engineer

Visium Resources, Inc.

Boulder, CO • On-site

Contractor

Re-posted 28 days ago

Job description

Introduction
Visium Resources has been asked to identify qualified candidates for this Pharmaceutical Senior CQV Engineer position. This position is a direct hire and worksite is in on-site in Boulder, CO. Employer will consider monthly expenses for the right candidate to commute to this location.


Summary

We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The successful candidate will lead and execute CQV deliverables associated with GMP-regulated process equipment, utilities, automation systems, cleanrooms, and manufacturing operations.

This role requires hands-on technical expertise, strong project coordination skills, and a thorough understanding of FDA and cGMP compliance requirements. The Senior CQV Engineer will work cross-functionally with Engineering, Quality, Manufacturing, Automation, and external vendors to ensure successful project execution and operational readiness within fast-paced life sciences environments.


Key Responsibilities
  • Lead and execute CQV activities for pharmaceutical and biotech capital projects. 
  • Develop and execute: 
    • Commissioning plans 
    • IQ/OQ/PQ protocols 
    • Validation test scripts 
    • Traceability matrices 
    • Summary reports 
  • Support startup and qualification of: 
    • Process equipment 
    • Clean utilities 
    • HVAC systems 
    • Manufacturing suites 
    • Automation and control systems 
  • Coordinate field execution activities with engineering, construction, vendors, and operations teams. 
  • Perform system walkdowns and turnover package reviews. 
  • Support deviation investigations, CAPAs, and change control activities. 
  • Ensure all validation documentation complies with cGMP, FDA, ISPE, and GAMP guidelines. 
  • Participate in FAT/SAT execution and acceptance activities. 
  • Support project schedule development and milestone tracking. 
  • Collaborate with Quality Assurance and Manufacturing teams to support inspection readiness and successful system release. 
  • Mentor junior CQV engineers and validation specialists as needed. 

Required Qualifications
  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, or related technical discipline. 
  • 5-10+ years of CQV, validation, or pharmaceutical engineering experience within GMP-regulated environments. 
  • Strong knowledge of: 
    • cGMP regulations 
    • FDA validation requirements 
    • ISPE Baseline Guides 
    • GAMP 5 principles 
  • Experience executing commissioning and qualification for: 
    • Process equipment 
    • Utilities 
    • HVAC systems 
    • Cleanrooms 
    • Automation systems 
  • Experience authoring and reviewing validation lifecycle documentation. 
  • Strong technical writing and documentation skills. 
  • Ability to work independently within fast-paced project environments. 

Preferred Qualifications
  • Experience in biologics, sterile manufacturing, fill-finish, or aseptic processing environments. 
  • Previous consulting experience within life sciences industries preferred. 
  • Familiarity with: 
    • DeltaV 
    • MES systems 
    • SCADA platforms 
    • Kneat or electronic validation systems 
  • PMP certification or equivalent project leadership experience is a plus. 
  • Strong client-facing communication and leadership skills. 

Additional Skills & Competencies
  • Excellent organizational and multitasking abilities 
  • Strong problem-solving and analytical skills 
  • Ability to manage multiple priorities and deadlines 
  • Comfortable working in both office and field environments 
  • Ability to travel to client sites as required 

________________________________________________________________________________________________


Visium Resources is an award-winning employment firm with a mission to match talented individuals with highly successful organizations. At Visium, our company's success is based on your success. When you work with us, you are never 'just a number'. You are our most important asset. Here, you will know us by name through our regular visits to client sites and even occasional luncheons. We will always be there when you need assistance and will always go the extra mile to ensure that you are as successful as possible. Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe there is no employment agency that will work harder for you than Visium.
Visium Resources is an equal opportunity employer and values diversity. All employment is decided based on qualifications, merit and business need.

Education:BS/BA DegreeEmployment Type: CONTRACTOR

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