Laboratory Metrology Technician (Part-Time)

Eurofins Clinical Trial Solutions; Lenexa (KS); On-site; USD 27,552 - 41,328; Part time

Benefits offered by this job

Comprehensive medical coverage

401(k) with company match

Paid vacation and holidays

Job summary

A leading life sciences company is seeking a part-time Laboratory Metrology Technician in Lenexa, Kansas. The ideal candidate will perform instrument maintenance, cleaning, and adherence to regulatory standards while supporting laboratory operations. Responsibilities include maintaining equipment, documenting actions, and ensuring compliance with quality standards. This role offers a flexible schedule with overtime potential and comprehensive benefits. Candidates must have experience in a regulated laboratory setting and possess strong communication and organizational skills.

Qualifications

• 2 years’ experience in a regulated laboratory is preferred.
• Comfortable working in a laboratory setting.
• Knowledge of basic computer programs such as Microsoft Word.

Responsibilities

• Perform and assist with instrument maintenance.
• Document cleaning and maintenance records.
• Conduct instrument calibration activities.

Skills

Instrument maintenance

Cleaning and calibration

Attention to detail

Regulatory compliance

Communication skills

Education

GED or High School Diploma

BA/BS in biological, physical, chemical or clinical laboratory science

Tools

Microsoft Excel

Laboratory equipment

Job description

Laboratory Metrology Technician (Part‑Time)

Eurofins Scientific is an international life sciences company that provides a unique range of analytical testing services. We support clients across food, environment, pharmaceuticals and cosmetic product testing, ensuring safety, authenticity and accurate labeling.

Job Description

The Laboratory Metrology Technician (Tech) supports Viracor laboratories, maintaining CLIA, CAP, NYDOH, GxP accreditation. The role involves instrument maintenance, cleaning, calibration, preventive maintenance, documentation of excursions, and compliance with regulatory requirements.

Responsibilities

Level I

• Perform and/or assist with instrument maintenance such as plate readers, washers, liquid handling equipment, front‑end lab automation, centrifuges, balances, etc.
• Responsible for cleaning laboratory areas and equipment and documenting it.
• Perform periodic maintenance and cleaning on ULT freezers, refrigerators and cryostorage equipment.
• Maintain cleaning and maintenance records as required.
• Perform instrument calibration activities and documentation, including environmental monitoring systems and laboratory equipment as directed (pipettes/temperature probes).
• Respond to and document environmental alerts, ensuring actions are logged and escalated when needed.
• Maintain instrument power cycles/UPS as required.
• Manage inventory of pipettes, supplying backups and replacements as requested.
• Document actions and maintain schedule of required activities in equipment tracking software.
• Perform administrative duties within the department and assist with audit documentation.
• Obtain and maintain proficiency in software programs or tools used in the department.
• Support development of systems and process improvements to enhance compliance.
• Adhere to all quality and safety standards and applicable regulatory agencies.
• Follow laboratory policies and protocols.
• Work closely with other laboratory associates to complete daily activities efficiently.
• Represent the department and the organization in accordance with company standards.
• Perform other duties as assigned by management.

Level II

• Fully meets Level I responsibilities and demonstrates high proficiency in multiple processes managed by the department.
• Train, assist users or clients with questions and/or issues; participate in validation of updates.
• Provide training and orientation of testing personnel on pipettes and environmental monitoring.
• Maintain laboratory equipment schedules, including calibration/maintenance tracking program/software, temperature monitoring system and pipette calibration program, ensuring calibrations are current.
• Understand and demonstrate proficiency with quality monitoring activities such as quality indicators and reporting.
• Communicate Metrology area needs to Facilities, Testing and Manufacturing personnel.
• Contact suppliers/vendors as required.
• Participate in data reporting, internal or external client reports, using Excel or other software for trend tracking.
• Participate in continual quality improvement projects company‑wide.
• Create/ revise SOPs and training materials for the department and update policies for regulatory changes.
• Perform other duties as assigned by management.

Qualifications

Basic Minimum Education

• 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 role.
• 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.
• Ability to maintain detailed and accurate records with great attention to detail.
• Position may require working hours outside of the normal 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 and 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 Possess the Following

• Ability to work independently and as part of an integrated quality team.
• 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.
• Work proactively in a self‑directed manner, taking initiative as required.
• Make sound decisions with little or no supervision, generating test data, performing analysis, and escalating when appropriate.

Physical Requirements

• Physical dexterity to operate keyboard, use telephone, access file cabinets, and move items at various levels.
• Speak and hear well enough to communicate clearly in normal conversational distance, over the telephone, and in a group setting.
• Stand for extended periods of time as necessary in the laboratory (4+ hours).
• Lift and move items weighing up to 50 pounds; push/pull heavy loads (may be >100 pounds) with assistance as available.
• Operate personal computer continuously for extended periods (4+ hours).
• Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, and make valid judgments and decisions.

Benefits

• Part‑time position with overtime as needed (Thursday–Saturday 7:00 pm–11:00 pm; Sunday 3:00 pm–11:30 pm).
• 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.

EEO Statement

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