Labcorp is seeking a
Validation Specialist
to join our team in Flow Cytometry for a 12-month contract in Geneva.
Work Schedule Monday-Friday
Job Responsibilities
Instruments/Equipment:
Demonstrate working knowledge of Flow Cytometers, centrifuges, biological safety cabinet, and pipettes in the department.
Able to provide troubleshooting to resolve complex instrument and equipment problems. Work with the vendor where needed to resolve issues and summarizes results of investigations.
Perform cytometer instrument setup and QC according to SOP.
Perform various laboratory maintenance tasks in collaboration with operations.
Training:
Coordinate timely review of SOPs, checklists, and other training materials.
Seek to promote expertise in the department and across sites to ensure consistent approach to validation of assays.
Successfully complete, as scheduled, competency assessment, and ensure competency testing documentation is provided to management for review/retention.
Competently perform department duties as set forth in the department training checklist(s).
SOPs/Validation Plans/Validation Reports:
Support with the writing of validation plans, reports, and SOPs with assistance from staff and Lead scientists.
Appropriately document work performed in compliance with Labcorp SOPs (generate appropriate audit trail for all activities).
Participate in meetings as requested by listening, discussing, and critically evaluating own data and that presented by others.
Interact with scientists to prepare client facing materials (timelines, datasets, and presentations).
Assay Development and Validation:
Perform specific validations-related laboratory tasks within timelines assigned by Staff and/or Lead scientist.
Maintain laboratory and project related inventory.
Assist Staff and Lead scientist with developing project reagent order plans (participate to the identification and the sourcing of reagents/commercial samples/equipment needed for assay validation. Requesting quotes to the Procurement team and interacting with vendors when needed)
Assist Staff and/or Lead scientist with the generation and organization of project data for client review.
Additional responsibilities:
Adhere to established Safety policies and Universal Precaution guidelines at all times. Maintain a clean, organized and safe work environment. Minimize biohazard waste.
Comply with regulatory guidelines and Labcorp Standard Operating Procedures (SOPs) at all times.
Minimum Qualifications
CFC, BTS, Bachelor, DUT or BUT degree holder.
6 months or more of flow cytometry laboratory experience.
6 months or more of Microsoft Excel and Word experience.
Preferred Qualifications
6 months or more of pipetting experience.
Additional Job Standards
Excellent verbal and written skills.
Good command of English and French.
Equal Opportunity Statement Labcorp is an Equal Opportunity Employer. We strive for inclusion and belonging.
Labcorp makes employment decisions based on the needs of the business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, pregnancy, childbirth, related medical conditions, family or parental status, marital status, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
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Validation Specialist
to join our team in Flow Cytometry for a 12-month contract in Geneva.
Work Schedule Monday-Friday
Job Responsibilities
Instruments/Equipment:
Demonstrate working knowledge of Flow Cytometers, centrifuges, biological safety cabinet, and pipettes in the department.
Able to provide troubleshooting to resolve complex instrument and equipment problems. Work with the vendor where needed to resolve issues and summarizes results of investigations.
Perform cytometer instrument setup and QC according to SOP.
Perform various laboratory maintenance tasks in collaboration with operations.
Training:
Coordinate timely review of SOPs, checklists, and other training materials.
Seek to promote expertise in the department and across sites to ensure consistent approach to validation of assays.
Successfully complete, as scheduled, competency assessment, and ensure competency testing documentation is provided to management for review/retention.
Competently perform department duties as set forth in the department training checklist(s).
SOPs/Validation Plans/Validation Reports:
Support with the writing of validation plans, reports, and SOPs with assistance from staff and Lead scientists.
Appropriately document work performed in compliance with Labcorp SOPs (generate appropriate audit trail for all activities).
Participate in meetings as requested by listening, discussing, and critically evaluating own data and that presented by others.
Interact with scientists to prepare client facing materials (timelines, datasets, and presentations).
Assay Development and Validation:
Perform specific validations-related laboratory tasks within timelines assigned by Staff and/or Lead scientist.
Maintain laboratory and project related inventory.
Assist Staff and Lead scientist with developing project reagent order plans (participate to the identification and the sourcing of reagents/commercial samples/equipment needed for assay validation. Requesting quotes to the Procurement team and interacting with vendors when needed)
Assist Staff and/or Lead scientist with the generation and organization of project data for client review.
Additional responsibilities:
Adhere to established Safety policies and Universal Precaution guidelines at all times. Maintain a clean, organized and safe work environment. Minimize biohazard waste.
Comply with regulatory guidelines and Labcorp Standard Operating Procedures (SOPs) at all times.
Minimum Qualifications
CFC, BTS, Bachelor, DUT or BUT degree holder.
6 months or more of flow cytometry laboratory experience.
6 months or more of Microsoft Excel and Word experience.
Preferred Qualifications
6 months or more of pipetting experience.
Additional Job Standards
Excellent verbal and written skills.
Good command of English and French.
Equal Opportunity Statement Labcorp is an Equal Opportunity Employer. We strive for inclusion and belonging.
Labcorp makes employment decisions based on the needs of the business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, pregnancy, childbirth, related medical conditions, family or parental status, marital status, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
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Validation Specialist - 12 months Arbeitgeber: Labcorp
Labcorp ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern die Möglichkeit bietet, in einem dynamischen Umfeld zu arbeiten, das sich auf Innovationen im Gesundheitswesen konzentriert. Mit umfassenden Vorteilen wie flexiblen Arbeitszeiten, einem attraktiven Vergütungspaket und umfangreichen Wachstumschancen fördert Labcorp eine inklusive Unternehmenskultur, in der jeder Mitarbeiter geschätzt wird und einen bedeutenden Beitrag zur Verbesserung der Gesundheit leisten kann. Die Position des Sr. Lead IT Product Manager in Durham, NC oder remote ermöglicht es Ihnen, an vorderster Front der Digitalisierung im Gesundheitswesen zu stehen und Ihre Karriere in einem globalen Unternehmen voranzutreiben.
