Environmental Monitoring Technician

About the Role

This position 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 role 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?

At Leiters Health, we're pioneers in the pharmaceutical field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety drives everything we do.

• Innovative Culture: Be part of a forward-thinking company that encourages creativity and fosters continuous improvement.
• Meaningful Work: Contribute to a purpose-driven organization providing critical medications that positively impact patients' lives.
• Professional Development: Access ongoing training, mentorship, and growth opportunities in a rapidly growing industry.
• Cutting-Edge Technology: Work with state-of-the-art facilities and advanced technologies.
• Collaborative Environment: Join a team of passionate individuals dedicated to teamwork, support, and mutual success.

Responsibilities

• Perform daily quality functions, including environmental monitoring of personnel and clean rooms.
• Incubate, enumerate, and verify 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.

Requirements

• High school diploma or GED required.
• 0-2 years of experience in a quality position at a cGMP facility (sterile injectable product preferred; food, cosmetic, or pharmaceutical experience 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.
• Proficiency with Microsoft 365 tools including Outlook, Word, 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.

Schedule

3:30 PM – 12:00 AM