Environmental Monitoring Technician

Leiters Inc; Englewood (CO); On-site; USD 30,000 - 35,000; Full time

Job summary

Leiters Health is hiring an Environmental Monitoring Technician in Englewood, CO. The role focuses on maintaining a compliant, sterile manufacturing environment and performing daily quality functions such as environmental monitoring, agar plate work, and investigations.

Strong communication and Excel skills are valued, with a path for growth in a fast-paced pharmaceutical setting. The position supports a collaborative, mission-driven team dedicated to high-quality sterile products and healthcare

Qualifications

• High school diploma or GED required; 0–2 years in a quality role preferred.
• Familiarity with cGMP, USP guidelines, and 503B expectations is a plus.
• Proficient in documenting data accurately and communicating across teams.

Responsibilities

• Perform daily environmental monitoring and maintain sterile lab conditions.
• Incubation, enumeration, and verification of agar plates.
• Support investigations for deviations or errors.
• Assist with media fills and observe filled units; follow SOPs and GMP training.

Skills

Communication

Adaptability

Data recording

Attention to detail

Education

High school diploma or GED

Tools

Microsoft 365

Excel

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Full-time Regular Englewood, CO, US

2 days ago Requisition ID: 1961

Salary Range: $22.00 To $25.29 Hourly

The Environmental Monitoring Technician reports to the Microbiology Manager and is responsible forperforming quality activities andmaintaininga quality laboratory environment in a sterile pharmaceutical manufacturing facility.The candidate should have an understanding of cGMP requirements and cleanroom cleanliness requirements.The position requires an individual who works independently and in a team environment, with attention to detail, andmaintainscommunication with other functional areas,leadershipand sites.

Are you passionate about making a real impact in the pharmaceutical industry? Do you thrive in a collaborative, innovative environment where your skills and ideas are valued? Look no further – Leiters Health is seeking talented individuals like you to join our dynamic team!

At Leiters Health, we're not just another pharmaceutical company – we're pioneers in the field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety is at the core of everything we do.

• Innovative Culture: Be part of a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement.
• Meaningful Work: Contribute to a purpose-driven organization dedicated to providing critical medications and healthcare solutions that positively impact patients' lives.
• Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry.
• Cutting-Edge Technology: Work with state-of-the-art facilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing.
• Collaborative Environment: Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration.

Who We're Looking For:

We're seeking enthusiastic individuals who are driven, adaptable, and passionate about contributing to a mission-driven organization. Whether you're an experienced professional or just starting your career, Leiters Health provides an environment where your skills and talents will be recognized and appreciated.

Essential Functions:

This description is intended to be illustrative of the major duties performed by the employee assigned to this position.

• Responsible for performing daily quality functions including:
• Performing environmental monitoring of personnel and clean rooms.
• Incubation, enumeration, and verification of agar plates.
• Support investigations when deviations or errors occur.
• Support process and operator media fills by enumerating, incubating, andobservingmedia filled units.
• Comprehend and utilize SOPs, forms, operational GMP training, and quality activities.
• Other duties as assigned.

SUPERVISORY RESPONSIBILITIES:

• N/A

EXPERIENCE AND NECESSARY COMPETENCIES:

• High school diploma or GED required.
• 0-2 years of a quality position at a cGMP facility. Sterile injectable product preferred. Food,cosmeticorpharmaceuticalwill be considered.
• Ability to communicate with multiple departments.
• Ability to adapt to changing priorities and circumstances.
• Able to consistently record critical data correctly and legibly.
• Understandingof503B regulatory requirements, cGMP standards, and USP guidelines is a plus!
• Proficient written, verbal and oral English communication skills are required.
• Proficiency with Microsoft 365 tools including Outlook, Microsoft, and Excel.

Physical Requirements:

• Ability to stand or sit for extended periods of time.
• Ability to lift, push and pullup to50 pounds periodically.
• Ability to maintain a gowning qualification.
• Must have 20/20near range vision and proficient color perception, with or without correction.