Job Description
Position Summary
The EQ Technician I is responsible for performing routine and non-routine testing in support of all aspects of the manufacturing operations including but not limited to the utility systems, sterilizer systems, incoming raw materials, in-process product solutions and final product solutions while adhering to safety, standard operating procedures (SOPs), standard test methods (STMs) and specifications, current good manufacturing practices (cGMP), standard laboratory practices (SLP), current good documentation practices (cGDP) and plant policies/guidelines. The EQ Technician I will work under direct supervision or lead.
Essential Duties & Responsibilities
- Perform microbiological and biological testing according to SLPs, STMs and SOPs. Test types (when applicable) include but are not limited to bioburden for pre-sterilized product and raw bulk drug utilizing membrane filtration and/or direct plate inoculation, non-viable particulate (liquid and air mediums), viable particulate (air medium), environmental and utilities systems monitoring (e.g., floors, equipment, oil-free compressed gas), growth promotion of purchased and prepared media, gram staining, organism culture creation and maintenance, and non-viable particulate matter identification. Techniques utilized include but are not limited to pour plating, handling and maintaining organism cultures, membrane filtration and direct plate inoculation, aseptic, and plate reading.
- Utilization and maintenance of laboratory instruments and equipment in support of routine and non-routine testing such according to SLPs, STMs, and SOPs. Instruments/equipment (when applicable) include but are not limited to non-viable particle counters for liquid and air mediums (e.g., HIAC, CLIMET), viable particle counters for air medium (e.g., Surface Air Sampler (SAS)), depyrogenation oven, steam sterilizer, pipettes (e.g., fixed, variable), waterbath (e.g., oil, water), compound light microscope, stereomicroscope, centrifuge, barcode scanners, label printers, stir/hot plates, timers/stopwatches, laminar airflow hoods (LAF) and biosafety cabinets (BSC).
- Generate and maintain accurate manual (hardcopy) documents such as batch records and other controlled worksheets and electronic laboratory records of tasks completed and review and/or verify the results of other laboratory personnel according to cGDP, SLPs, STMs and SOPs. Generation and maintenance of such records include compliant utilization of databases and software applications such as PharmSpec, MODA or other laboratory information management system (LIMS) such as Labware, Oracle, Microsoft (e.g., Access), and Excel (e.g., validated spreadsheets).
- Provide support in the resolution of manufacturing (production) problems, the execution of technical studies, and during laboratory investigations. Identify and escalate questionable or inconsistent results to the supervisor/manager or other designee such as lead laboratory technician(s). Participate in evaluating and clarifying problems and provide suggestions for resolution. Includes safety related items.
- Maintain and prepare media/materials in accordance with SOPs including sterilization of liquid and hard goods items. Includes decontamination and other sterilization cycle types as applicable.
- Work on special projects as they arise.
- Perform tasks outside of primary job duties on an as-needed basis or per business/departmental needs. This will include, but is not limited to, cross-training in Biological Quality laboratories/functions and participation in special projects.
Knowledge & Skills
- Requires an understanding of laboratory instrumentation and methodologies including microbiology and environmental science(s). Must maintain a high regard for detail, timeliness, and accuracy of all testing and associated documentation.
- Must be able to read, understand, and execute instructions in basic laboratory procedures.
- Must be able to use mathematics to solve routine problems and execute algebraic equations daily.
- Must be able to perform tests quickly and efficiently without sacrificing accuracy, safety, or quality.
- Must be able to use Microsoft Office (i.e., Word, Excel) and have aptitude to learn internal systems.
- Must recognize, communicate, and appropriately respond to inconsistent and nonconformance results.
- Must utilize sound judgment in making decisions within limitations of recognized STMs and SOPs.
- Must communicate effectively and proficiently at all levels both within and outside the plant. The individual is required to organize communication in a logical manner and explain technical information to non-technical individuals.
- Must have demonstrated a high degree of personal maturity, reliability, and professional judgment.
Minimum Qualifications, Education & Experience
- Must be at least 18 years of age.
- High school diploma is required.
- Minimum of 2 years of experience in biological/environmental laboratory environment is preferred.
Work Environment
- Work is performed in a laboratory as well as cleanroom environment and other manufacturing areas; work is performed while wearing specified personal protective equipment (PPE) and other gowning attire as applicable (e.g., safety glasses, lab coat, cleanroom attire).
- Work is performed with microorganisms (as applicable) as well as instruments and equipment which may contain lasers or utilize steam and/or vacuum/pressurized.
- While performing the duties of this job, the employee may be required to sit or stand for long periods of time depending on the given activity.
- Required to use a computer or touch screen to execute or enter work/data.
- Must be able to occasionally move and lift objects of up to 25 pounds (lbs.).
- Typically requires travel less than 5% of the time
About Us
ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.
With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.
We're Ready To Bring You Consistent Quality, Innovation, And Value In More Areas Than Ever. Our Focus Allows Us To Bring You
- Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
- The industry’s broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
- IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
- Significant US IV solutions manufacturing and supply capabilities.
ICU Medical EEO Statement
ICU Medical is committed to fostering a diverse, inclusive, and equitable work environment. As an Affirmative Action and Equal Opportunity Employer, we ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender identity, gender expression, gender reassignment, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.
If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.
ICU Medical EEO Policy Statement
OFCCP Equal Opportunity Posters
- “Know Your Rights” Poster
- Pay Transparency Nondiscrimination Provision
ICU Medical CCPA Notice to Job Applicants
