Environmental Monitoring Technician

Leiters Inc•Englewood, CO

5d•$22 - $25•Onsite

About The Position

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. Leiters Health is a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement. We are 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. We offer ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. You will work with state-of-the-art facilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing. Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration.

Requirements

High school diploma or GED required.
0-2 years of a quality position at a cGMP facility.
Ability to communicate with multiple departments.
Ability to adapt to changing priorities and circumstances.
Able to consistently record critical data correctly and legibly.
Proficient written, verbal and oral English communication skills are required.
Proficiency with Microsoft 365 tools including Outlook, Microsoft, and Excel.
Ability to maintain a gowning qualification.
Must have 20/20 near range vision and proficient color perception, with or without correction.

Nice To Haves

Sterile injectable product preferred.
Food, cosmetic or pharmaceutical experience will be considered.
Understanding of 503B regulatory requirements, cGMP standards, and USP guidelines is a plus!

Responsibilities

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.