Eurofins Viracor BioPharma Services
Laboratory Metrology Technician (Part-Time)
Eurofins Viracor BioPharma Services, Lenexa, Kansas, United States
Laboratory Metrology Technician (Part-Time)
Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries. From the food you eat to the water you drink to the medicines you rely on, Eurofins laboratories work with the largest companies worldwide to ensure the products they supply are safe, authentic, and accurately labelled.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing, agroscience, contract research organizations, and contract development and manufacturing. With over 30 years of growth, we currently operate 900 laboratories in more than 54 countries and offer a portfolio of over 200,000 analytical methods.
Members of the Metrology team support laboratories at Viracor by maintaining CLIA, CAP, NYDOH, and GxP accreditation. The Laboratory Metrology Technician is responsible for conducting and documenting cleaning, calibration, preventive maintenance, and recording excursions from expected performance.
Responsibilities Level I
Perform and/or assist with instrument maintenance such as plate readers, washers, liquid‑handling equipment, front‑end lab automation equipment, centrifuges, balances, etc.
Perform and document cleaning of laboratory areas and equipment.
Perform periodic maintenance and cleaning on ULT freezers, refrigerators and cryostorage equipment.
Maintain cleaning and maintenance records.
Conduct instrument calibration activities and documentation, including environmental monitoring systems and lab equipment such as pipettes and temperature probes.
Respond to and document environmental alerts, ensuring documentation of actions taken or escalation as needed.
Maintain instrument power cycles and UPS as required.
Manage inventory of pipettes, supplying backups and replacements as requested.
Maintain proper records in equipment‑tracking software, documenting actions and maintaining schedules of required activities.
Perform administration duties within the department and provide documentation during investigations and audits.
Obtain and maintain proficiency in software programs or tools used in the department.
Support development of systems and process improvements that enhance compliance.
Adhere to all quality and safety standards, including regulatory agency requirements.
Adhere to laboratory policies and protocols.
Work closely with other laboratory associates to complete daily activities efficiently.
Represent the department and organization favorably in accordance with company standards.
Other duties as assigned by management.
Level II
Fully meet all Level I responsibilities.
Highly proficient in multiple processes managed by the department.
Train, assist users or clients with questions, and participate in validation of updates.
Provide training and orientation to testing personnel as directed (e.g., pipettes, environmental monitoring).
Maintain laboratory equipment schedules, including calibration, maintenance tracking software, temperature monitoring systems, and pipette calibration programs.
Understand and demonstrate proficiency with quality monitoring activities such as KPIs for quality meetings.
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 reporting software.
Participate in continual quality improvement projects company‑wide.
Participate in creation or revision of SOPs and training materials, ensuring policies are updated to reflect regulatory changes.
Other duties as assigned by management.
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.
Knowledge of the clinical laboratory environment (terminology, protocols, practices) preferred.
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, according to good documentation practices.
Position may require working hours outside the normal work schedule when necessary.
Ability to keep sensitive information confidential.
Working knowledge of good laboratory practices and 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 Candidate Possesses the Following
Ability to work both 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.
Proactive, self‑directed, and able to take initiative as required.
Make sound decisions with little or no supervision, including data generation, analysis, and escalation.
Physical Requirements
Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment.
Ability to speak and hear well enough to communicate clearly and understandably.
Ability to stand for extended periods in the laboratory (4 or more hours).
Ability to lift and move items weighing up to 50 pounds.
Use assistance as available to push/pull heavy loads (may exceed 100 pounds).
Move body frequently around laboratory equipment and instrumentation.
Operate a personal computer continuously for extended periods.
Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, and make judgments and decisions.
Position Part‑time, working Thursday‑Saturday: 7:00 pm – 11:00 pm and Sunday 3:00 pm – 11:30 pm, with overtime as needed. Candidates currently living within a commutable distance of Lenexa, KS are encouraged to apply.
Benefits
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.
Employment Details
Seniority level: Entry level.
Employment type: Part‑time.
Job function: Management and Manufacturing.
Referrals increase your chances of interviewing at Eurofins Viracor BioPharma Services by 2×.
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The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing, agroscience, contract research organizations, and contract development and manufacturing. With over 30 years of growth, we currently operate 900 laboratories in more than 54 countries and offer a portfolio of over 200,000 analytical methods.
Members of the Metrology team support laboratories at Viracor by maintaining CLIA, CAP, NYDOH, and GxP accreditation. The Laboratory Metrology Technician is responsible for conducting and documenting cleaning, calibration, preventive maintenance, and recording excursions from expected performance.
Responsibilities Level I
Perform and/or assist with instrument maintenance such as plate readers, washers, liquid‑handling equipment, front‑end lab automation equipment, centrifuges, balances, etc.
Perform and document cleaning of laboratory areas and equipment.
Perform periodic maintenance and cleaning on ULT freezers, refrigerators and cryostorage equipment.
Maintain cleaning and maintenance records.
Conduct instrument calibration activities and documentation, including environmental monitoring systems and lab equipment such as pipettes and temperature probes.
Respond to and document environmental alerts, ensuring documentation of actions taken or escalation as needed.
Maintain instrument power cycles and UPS as required.
Manage inventory of pipettes, supplying backups and replacements as requested.
Maintain proper records in equipment‑tracking software, documenting actions and maintaining schedules of required activities.
Perform administration duties within the department and provide documentation during investigations and audits.
Obtain and maintain proficiency in software programs or tools used in the department.
Support development of systems and process improvements that enhance compliance.
Adhere to all quality and safety standards, including regulatory agency requirements.
Adhere to laboratory policies and protocols.
Work closely with other laboratory associates to complete daily activities efficiently.
Represent the department and organization favorably in accordance with company standards.
Other duties as assigned by management.
Level II
Fully meet all Level I responsibilities.
Highly proficient in multiple processes managed by the department.
Train, assist users or clients with questions, and participate in validation of updates.
Provide training and orientation to testing personnel as directed (e.g., pipettes, environmental monitoring).
Maintain laboratory equipment schedules, including calibration, maintenance tracking software, temperature monitoring systems, and pipette calibration programs.
Understand and demonstrate proficiency with quality monitoring activities such as KPIs for quality meetings.
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 reporting software.
Participate in continual quality improvement projects company‑wide.
Participate in creation or revision of SOPs and training materials, ensuring policies are updated to reflect regulatory changes.
Other duties as assigned by management.
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.
Knowledge of the clinical laboratory environment (terminology, protocols, practices) preferred.
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, according to good documentation practices.
Position may require working hours outside the normal work schedule when necessary.
Ability to keep sensitive information confidential.
Working knowledge of good laboratory practices and 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 Candidate Possesses the Following
Ability to work both 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.
Proactive, self‑directed, and able to take initiative as required.
Make sound decisions with little or no supervision, including data generation, analysis, and escalation.
Physical Requirements
Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment.
Ability to speak and hear well enough to communicate clearly and understandably.
Ability to stand for extended periods in the laboratory (4 or more hours).
Ability to lift and move items weighing up to 50 pounds.
Use assistance as available to push/pull heavy loads (may exceed 100 pounds).
Move body frequently around laboratory equipment and instrumentation.
Operate a personal computer continuously for extended periods.
Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, and make judgments and decisions.
Position Part‑time, working Thursday‑Saturday: 7:00 pm – 11:00 pm and Sunday 3:00 pm – 11:30 pm, with overtime as needed. Candidates currently living within a commutable distance of Lenexa, KS are encouraged to apply.
Benefits
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.
Employment Details
Seniority level: Entry level.
Employment type: Part‑time.
Job function: Management and Manufacturing.
Referrals increase your chances of interviewing at Eurofins Viracor BioPharma Services by 2×.
#J-18808-Ljbffr