Laboratory Metrology Technician (2nd Shift)

Members of the Metrology team support processes for laboratories at Viracor with a focus on maintaining CLIA, CAP and NYDOH, GxP accreditation by using and maintaining procedures and software or other methods to perform, train, document, assist others to ensure complete and appropriate documentation of required tasks and records.

The Laboratory Metrology Technician (Tech) is responsible for conducting and documenting cleaning, calibration, preventive maintenance functions, and documenting excursions from expected performance as outlined by management in the laboratory areas

Laboratory Metrology Technician responsibilities include, but are not limited to, the following:

Level I –

• Perform and/or assist with instrument maintenance such as plate readers and washers, liquid handling equipment, front end lab automation equipment, centrifuges, balances, etc.
• Responsible for performing and documenting cleaning of the laboratory areas and equipment
• Perform periodic maintenance and cleaning on ULT freezers, refrigerators and cryostorage equipment.
• Maintain cleaning and maintenance records as required
• Instrument calibration activities and documentation including environmental monitoring system and laboratory equipment as directed (Pipettes/Temperature probes)
• Respond to and document environmental alerts, ensuring documentation of actions taken/escalate as needed
• Instrument power cycles/UPS maintenance as required
• Inventory management and upkeep of pipettes including supplying backups and replacements as requested
• Maintain proper records in equipment tracking software by documenting actions and maintaining schedule of required activities
• Administration duties within the department and investigation activities which includes providing documentation as requested by internal or external auditors
• Obtain and maintain proficiency in software programs or tools used in department
• Support development of system and process improvements that would enhance compliance to requirements
• Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies
• Adhere to policies and protocols in the laboratory
• Work closely and communicate with other laboratory associates to complete daily activities efficiently
• Represent department and the organization favorably and in accordance with established company standards and associate attributes at all times
• Other duties as assigned by management

Level II –

Fully meets the responsibilities of Level I plus the following:

• Highly proficient in multiple processes managed by the department
• Able to train, assist users or clients with questions and/or issues, participate in validation of updates
• Provide training and orientation of testing personnel as directed (pipettes and environmental monitoring)
• Maintenance of Laboratory equipment schedules, including management of calibration/maintenance tracking program/software, temperature monitoring system, and pipette calibration program, ensuring that calibrations are correct and current.
• Understand and demonstrate proficiency with quality monitoring activities such as quality indicators and quality reporting related to equipment and monitoring such as KPIs for Quality Meeting
• Communicates Metrology area needs to Facilities, Testing and Manufacturing personnel
• Contacts suppliers/vendors as required
• Participate in data reporting, internal or external client reports as requested, using Excel or other software utilized for reporting, trending, and tracking
• Participate in continual quality improvement projects company-wide
• Participate in creation/revision of SOPs and training materials for the department as required and ensure policies and procedures are monitored and updated to include regulatory changes
• Other duties as assigned by managemen

Basic Minimum Education Qualifications:

• Level I: GED or High school Diploma
• Level II: BA/BS in biological, physical, chemical or clinical laboratory science preferred.

Basic Minimum Qualifications:

• Level II: minimum of 2 years’ experience in a regulated laboratory (CAP/CLIA and/or GxP), as Laboratory Quality Tech I, or similar experience in Laboratory process ownership, e.g. laboratory technical roles.
• Knowledge of the clinical laboratory environment preferred, including basic terminology, protocols and practices
• Ability to initiate tasks and work efficiently with minimal supervision
• Comfortable working in a laboratory setting
• Knowledge of basic computer programs such as Microsoft Excel and Word including common applications in laboratory use
• Ability to maintain detailed and accurate records with great attention to detail, according to good documentation practices
• Position may require working hours outside of the normal work schedule when necessary
• Ability to keep sensitive information confidential
• Working knowledge of good laboratory practices and laboratory test methodologies.
• Ability to identify aberrant data and potential quality/compliance concerns escalating to management.
• Familiarity with six sigma scoring as applied to metrics/KPIs for quality
• Authorization to work in the United States indefinitely without restriction or sponsorship.

The Ideal Candidates Possesses the Following:

• Ability to work both independently and as part of an integrated quality team
• Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills
• Excellent verbal and written communication skills, including the ability to communicate effectively with all levels of the organization and with external customers/vendors when required
• Ability to work both independently and as part of an integrated quality team
• Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills
• Excellent verbal and written communication skills, including the ability to communicate effectively with all levels of the organization and with external customers/vendors when required
• Ability to work proactively in a self-directed manner, taking initiative as required
• Ability to make sound decisions with little or no supervision, including generating test data, performing analysis, and escalating when appropriate

Physical Requirements:

• Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead
• Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting
• Ability to stand for extended periods of time as necessary in the laboratory (4 or more hours)
• Ability to lift and move items weighing up to 50 pounds
• Using assistance as available, must have physical ability to push/pull heavy loads (may be in excess of 100 pounds
• Physical dexterity sufficient to move body frequently around laboratory equipment and instrumentation
• Ability to continuously operate a personal computer for extended periods of time (4 or more hours)
• Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, make valid judgments and decisions

Position is full-time working, Tuesday - Saturday 3:00pm-11:30pm, with overtime as needed. Candidates currently living within a commutable distance of Lenexa, KS are encouraged to apply.

• Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.