Environmental Monitoring Technician

Leiters Health; Denver (CO); On-site; USD 52,000 - 76,000; Full time

Job summary

Leiters Health is seeking an Environmental Monitoring Technician to join our sterile pharmaceutical operations in Denver. You will perform environmental monitoring of personnel and clean rooms, and support investigations into deviations while maintaining strict GMP and USP standards.

Responsibilities include incubating and enumerating agar plates, supporting media fills, and ensuring accurate data capture. Collaboration with multiple departments is essential to ensure product quality and patient

Qualifications

• High school diploma or GED is required.
• 0-2 years in a quality role at a cGMP facility; sterile injectable experience preferred.
• Must communicate across departments and adapt to changing priorities.
• Ability to record data accurately with good handwriting and digital logs.
• Understanding of 503B requirements, cGMP, and USP guidelines is a plus.

Responsibilities

• Perform daily environmental monitoring of personnel and clean rooms.
• Incubate, enumerate, and verify agar plates.
• Support investigations when deviations occur.
• Assist with media fills and observe filled units.
• Follow SOPs, GMP training, and quality activities.

Skills

Environmental monitoring

Agar plate incubation

CGMP familiarity

SOP adherence

Communication skills

Excel

Education

High school diploma or GED

Tools

Microsoft 365

Excel

Job description

The Environmental Monitoring Technician reports to the Microbiology Manager and is responsible for performing quality activities and maintaining a 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, and maintains communication with other functional areas, leadership and sites.

Why Join Leiters Health?

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, and observing media 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, cosmetic or pharmaceutical will 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.
• Understanding of 503B 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 pull up to 50 pounds periodically.
• Ability to maintain a gowning qualification.
• Must have 20/20 near range vision and proficient color perception, with or without correction.

3:30pm-12:00am