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Environmental Monitoring Jobs in Colorado (NOW HIRING)

STAQ Pharma Inc

Quality Control Technician

Denver, CO · On-site

$24/hr

The Quality Control Technician supports the QC function in a 503B pharmaceutical manufacturing environment by helping ensure materials, samples, documentation, and environmental monitoring activities ...

BELFOR Holdings

Field Safety Coordianator

Arvada, CO

$19.25 - $25.50/hr

Monitor specialized environmental monitoring equipment and industrial hygiene data.[Environmental Only] * Other projects and duties as assigned. Experience and Qualifications * High School Diploma or ...

Conagra Brands

Plant Sanitation Manager

Denver, CO · On-site

$82K - $120K/yr

Manage sanitation, environmental monitoring, and pest management programs, including trend analysis, effectiveness evaluations, and corrective action implementation. * Lead investigations involving ...

Conagra Brands, Inc.

Plant Sanitation Manager

Denver, CO · On-site

$82K - $120K/yr

Manage sanitation, environmental monitoring, and pest management programs, including trend analysis, effectiveness evaluations, and corrective action implementation. * Lead investigations involving ...

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Environmental Monitoring information

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How much do environmental monitoring jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for environmental monitoring in Colorado is $23.13, according to ZipRecruiter salary data. Most workers in this role earn between $18.22 and $26.54 per hour, depending on experience, location, and employer.

What is an environmental monitoring job?

An Environmental Monitoring job involves assessing and analyzing environmental conditions to ensure compliance with regulations and safety standards. Professionals in this role collect air, water, and soil samples, monitor pollution levels, and report findings to regulatory agencies or organizations. They work in industries such as manufacturing, healthcare, and government to prevent environmental hazards and protect public health. Strong analytical skills, attention to detail, and knowledge of environmental laws are essential for this role.

What does an environmental monitoring specialist do?

A typical day in Environmental Monitoring involves a mix of fieldwork and office-based tasks. You may spend time outdoors collecting samples of air, water, soil, or biological materials, followed by laboratory analysis or data entry using specialized software. Collaboration with scientists, engineers, and regulatory agencies is common, as is preparing detailed reports and ensuring compliance with environmental regulations. Depending on the employer, the workload can vary with project demands and environmental conditions, providing a dynamic and sometimes physically active work environment.

What are the key skills and qualifications needed for environmental monitoring?

To thrive in Environmental Monitoring, you need a solid background in environmental science or a related field, along with strong analytical and data interpretation skills. Familiarity with sampling equipment, environmental monitoring instruments, and relevant software such as GIS or data management systems is often required, as well as certifications like HAZWOPER in certain settings. Attention to detail, critical thinking, and strong communication skills are valuable soft skills for accurately documenting findings and collaborating with multidisciplinary teams. These skills ensure the accurate collection and analysis of environmental data, which is vital for compliance, public safety, and effective environmental management.

How to become an environmental monitoring technician?

To become an environmental monitoring technician, candidates typically need a high school diploma or equivalent, with some roles requiring an associate degree in environmental science, biology, or a related field. Relevant skills include knowledge of sampling techniques, data collection, and familiarity with environmental monitoring tools and software; certifications such as OSHA safety training or environmental sampling certifications can enhance job prospects. On-the-job training is common, and technicians often work outdoors in various weather conditions.

What does environmental monitoring do?

Environmental monitoring involves collecting data on air, water, soil, and other environmental factors to assess pollution levels, compliance with regulations, and overall environmental health. Professionals in this field use tools like sensors and sampling equipment and often require knowledge of environmental regulations and data analysis. The goal is to detect issues early and support sustainable practices.

What are the most commonly searched types of Environmental Monitoring jobs in Colorado?

The most popular types of Environmental Monitoring jobs in Colorado are:

What are popular job titles related to Environmental Monitoring jobs in Colorado?

For Environmental Monitoring jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Environmental Monitoring jobs in Colorado look for?

The top searched job categories for Environmental Monitoring jobs in Colorado are:

What cities in Colorado are hiring for Environmental Monitoring jobs?

Cities in Colorado with the most Environmental Monitoring job openings:

Environmental Monitoring jobs near you
Infographic showing various Environmental Monitoring job openings in Colorado as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $48,117 per year, or $23.1 per hour.

Quality Control Technician

STAQ Pharma Inc

Denver, CO • On-site

$24/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago

Key responsibilities

  • Coordinate QC sample preparation and shipment/submission of samples to external laboratories for testing activities.

  • Assist with environmental monitoring and microbiological sample evaluation activities, including organizing samples and reviewing forms.

  • Perform sampling and inspection of in-process and finished products according to approved procedures and quality expectations.

Job description


Position Summary:

The Quality Control Technician supports the QC function in a 503B pharmaceutical manufacturing environment by helping ensure materials, samples, documentation, and environmental monitoring activities are handled in accordance with cGMP, company procedures, and applicable regulatory requirements. This role provides hands-on support across QC, QA, and Operations, including coordinating QC sample preparation, external laboratory submissions, environmental monitoring support, retention material management, raw material and sterile supply release support, and review of GMP documentation. The QC Technician plays an important role in patient safety by helping verify that materials, environments, samples, and records meet quality expectations before they support manufacturing or product release.

What This Role Does Day-to-Day:

In this role, the QC Technician may support incoming material review, retention sample organization, sample preparation, environmental monitoring sample coordination, third-party laboratory submissions, biohazard waste coordination, logbook generation, GMP document review, and inspection activities for in-process or finished product samples. Daily work may include preparing and tracking samples, verifying documentation, using vendor portals or paper submissions for external testing, reviewing room and equipment logs, assisting with investigations, and communicating quality data or concerns to department leadership. The role requires strong attention to detail, accurate documentation, comfort working in or around cleanroom environments, and the ability to escalate issues that may impact product quality, compliance, or patient safety.

Key Responsibilities:

  • Coordinate QC sample preparation and shipment/submission of samples to external laboratories for environmental monitoring, microbiological, raw material, in-process, finished product, and other required testing activities.
  • Use third-party laboratory web portals, paper submission forms, and internal tracking tools to support accurate sample submission, chain-of-custody, and follow-up on required testing.
  • Assist with environmental monitoring and microbiological sample evaluation activities, including organizing samples, reviewing forms, and escalating missing, incomplete, or questionable information.
  • Maintain retention materials, including organization, tracking, storage support, and disposal when required by procedure.
  • Assist with review and release support for raw materials, APIs, excipients, sterile supplies, and other incoming materials as assigned.
  • Perform sampling and inspection of in-process and finished products according to approved procedures, sampling plans, and quality expectations.
  • Coordinate biohazard waste destruction activities in accordance with internal procedures and safety requirements.
  • Generate, issue, organize, or maintain logbooks and controlled documents as assigned.
  • Review GMP documents, including production environmental monitoring forms, room logs, equipment logs, sample forms, and related quality records for accuracy, completeness, and GDP expectations.
  • Support investigations, deviations, CAPAs, and continuous improvement activities by gathering information, reviewing documentation, and helping identify appropriate corrective or preventive actions.
  • Support quality management system activities, including document control, training program support, and cross-functional quality initiatives.
  • Work closely with Production, QA, QC, Warehouse, and external laboratory vendors to support timely sample flow, material review, documentation accuracy, and quality communication.
  • Identify and escalate potential documentation errors, sample discrepancies, environmental monitoring concerns, material issues, or process deviations to the appropriate quality leadership.
  • Follow all applicable cGMP, GDP, SOP, OSHA, FDA, and company policy requirements.
  • Perform other duties as assigned based on business and quality needs.

What Success Looks Like: 

  • Maintains accurate, organized, and traceable QC records, sample documentation, logbooks, and submission information.
  • Understands that sample handling, environmental monitoring support, and documentation accuracy directly impact patient safety and product quality.
  • Follows procedures carefully and asks for clarification before proceeding when information is unclear or does not match expectations.
  • Communicates clearly with QC, QA, Production, Warehouse, and third-party laboratories to keep quality activities moving forward.
  • Identifies and escalates quality concerns, missing documentation, sample discrepancies, or potential deviations in a timely manner.
  • Balances urgency with compliance and does not sacrifice accuracy, documentation, or safety to move work faster.
  • Demonstrates strong attention to detail, professionalism, reliability, and a willingness to learn within a regulated manufacturing environment.
  • Supports continuous improvement by identifying opportunities to improve sample tracking, documentation flow, communication, and quality processes.

Required Qualifications:

  • Associate degree in the sciences or equivalent experience preferred.
  • At least 1 year of Quality Control Technician experience preferred.
  • Pharmaceutical, medical device, biotechnology, laboratory, sterile manufacturing, or regulated manufacturing experience preferred.
  • Familiarity with cGMP, GDP, FDA-regulated environments, quality documentation, or controlled procedures preferred.
  • Strong attention to detail and ability to review records, forms, and logs for completeness and accuracy.
  • Excellent written, verbal, interpersonal, and independent judgment skills.
  • Ability to work in a fast-paced environment with changing priorities, competing deadlines, and cross-functional requests.
  • Proficiency with Microsoft Word, Excel, PowerPoint, Outlook, and ability to learn vendor portals or internal quality systems.
  • Must be able to speak, read, and write in English.
  • Must be a team player with a professional, quality-focused, and patient-safety mindset.

Physical Requirements: 

  • Ability to work in or around cleanroom and controlled manufacturing environments as required.
  • Ability to wear required PPE and follow gowning, cleanliness, and safety procedures.
  • Prolonged periods of sitting at a desk and working on a computer.
  • Ability to stand, walk, bend, reach, and handle samples, materials, or documentation as needed.
  • Ability to lift up to 15 pounds at times.

Work Environment: 

This position supports QC activities within a 503B pharmaceutical manufacturing environment and may involve work in cleanroom, controlled, laboratory support, warehouse, and office settings. Employees are expected to follow all applicable PPE, gowning, cleanliness, documentation, safety, and quality requirements. The role requires regular interaction with production areas, quality records, samples, materials, external laboratories, and cross-functional teams.

Benefits:

We offer a comprehensive and competitive benefits package designed to support the health, well-being, and financial security of our employees and their families.

At STAQ Pharma, all full time employees have access to:

  • Medical, dental, and vision insurance options
  • Employer-paid life insurance and disability coverage
  • Employee Assistance Program
  • 401(k) retirement plan with employer match
  • Paid time off (PTO), sick leave  
  • 7 paid holidays
  • Opportunities for professional growth in a regulated pharmaceutical manufacturing environment
  • Employee-focused culture emphasizing safety, quality, and teamwork


The application window for this position is anticipated to be open at least 25 days