ppLabcorp is seeking a bFlow Cytometry Analyst /b to join our team in Geneva, Switzerland. /p h3Work Schedule /h3 pTuesday–Saturday /p h3Job Responsibilities /h3 pbPerform assigned clinical laboratory flow cytometry analysis accurately and in a timely manner: /b /p ul lipResolve pendings. Retrieve and check specimens against pending list. Document specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved. /p /li lipPerform routine testing and calculations as required. /p /li lipResolve routine and non‑routine assay problems. /p /li /ul pbEnsure the validity of test results through the performance of established quality assurance and quality control procedures: /b /p ul lipPerform experiments, as scheduled, for evaluation of new Calibrator and/or QC lots. Summarize results of investigations and compile data for review by management. /p /li lipDocument quality control results. Interpret quality control results according to Westgard rules or other established departmental procedures and accurately document biases, warnings and violations of control values. /p /li lipDocument corrective action for unusual occurrences (e.g. QC violations, instrument‑related problems). /p /li lipAnalyze proficiency testing survey samples as patient specimens. /p /li /ul pbResult Entry (Auto‑verification and manual entry): /b /p ul lipWhen data is manually entered (e.g. QC, patient data) ensure peer review is performed and documented prior to release of results. /p /li lipPrepare proper documentation of test results and enter into the information system. /p /li lipGenerate an appropriate audit trail for all activities. /p /li lipDocument and communicate any result reporting problems or inconsistencies to laboratory management. /p /li lipComplete testing within the expected turnaround time to meet customer expectations. /p /li lipComply with regulatory guidelines and Labcorp Standard Operating Procedures (SOPs) at all times. /p /li /ul h3Training /h3 ul lipIndividual is responsible for maintaining his/her complete up‑to‑date training file and is accountable for correcting and deficiencies found in his/her training file. /p /li lipIndividual is responsible for ensuring he/she is trained and training is documented prior to performing a task. /p /li lipThe individual successfully completes, as scheduled, competency assessment and ensures competency testing documentation is provided to management for review/retention. /p /li lipCompetently perform department duties as set forth in the department training checklist(s). /p /li lipMay assist in training new employees and follows up to ensure training is understood. /p /li lipAttend, as scheduled, department, mandatory and other meetings and training, as required according to training matrices. /p /li /ul h3Work to achieve partnership with both internal customers and external clients by /h3 ul lipPull data in a timely manner for review by QA and external clients. /p /li lipContribute to the provision of accurate verbal or written response to internal QA and client audit findings. Coordinate, where needed, with other resources to resolve issue. /p /li lipResearch and prepare a response following investigation for quality purposes. Coordinate, where needed, with other resources to resolve issue. /p /li lipResearch and respond in a timely manner to internal customer inquiries regarding status of test results, retrieval of samples for testing/storage and other needs. /p /li lipUnderstand department metrics and goals. /p /li /ul pbMaintain a clean, organized and safe work environment. /b /p pbTake action for the department when additional responsibilities and opportunities are presented. /b /p pbProvide laboratory management with a report of activities upon request. /b /p pbOther duties as assigned. /b /p h3Minimum Qualifications /h3 ul lipMedical Technologist degree or Medical Biology degree (CFC, BTS, Bachelor, DUT, IUT degree holder) or Foreign Medical Technologist Degree with equivalency statement from Swiss Red Cross. /p /li /ul h3Preferred Qualifications /h3 ul lip6 months or more of experience in laboratory operations. /p /li lip6 months or more of experience in flow cytometry data analysis. /p /li /ul h3Additional Job Standards /h3 ul lipbIntermediate level in English, French is an asset. /b /p /li lipFamiliarity with FCSExpress, WinList or FlowJo. /p /li lipAttention to detail and good organizational skills. /p /li lipTeam player with an ability to work independently. /p /li /ul h3Labcorp is proud to be an Equal Opportunity Employer /h3 pLabcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our 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 (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, 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. /p pWe encourage all to apply. /p pIf you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see Privacy Statement. /p /p #J-18808-Ljbffr
