Environmental Monitoring Technician

The Environmental Monitoring Technician reports to the Microbiology Manager and is responsible for performing 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,leadership and 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!

• 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.

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.

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.

• N/A

• 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.
• 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.

• 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.

3:30pm-12:00am