Large

Clear and confident health care decisions begin with questions. At Labcorp, we’re constantly in pursuit of answers. 

With unparalleled diagnostics and drug development capabilities, we accelerate innovation and provide insight to improve health and improve lives. Whether you’re a patient, provider, researcher or in the pharmaceutical industry, we’re here for you. More than 70,000 employees strong, we serve clients in more than 100 countries. Labcorp (NYSE: LH) reported revenue of $14 billion in FY 2020.

Science & Healthcare

Labcorp

Healthcare Management

You need a high school diploma, strong data entry skills, comfort with biological specimens, attention to detail, team experience, and MS Office proficiency. Color blind test required.

You will enter patient results accurately, print daily worksheets, manage laboratory systems, store results properly, communicate with clients, order supplies, and perform additional clerical tasks.

Data

Healthcare

Raleigh

At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step! Labcorp is seeking a Data Entry Operator to join our team in RTP, NC. Work Schedule: first shift Tuesday-Saturday 9:30am to 6:00pm Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Job Responsibilities * Perform data entry of patient’s results in a timely and accurate manner * Print out and distribute daily worksheets for technical staff * Use various laboratory systems to enter test results * Ensure test results are stored in their proper location * Call client with test results when necessary * Order supplies for the department when need * Other administrative and clericals tasks as required Job Requirements * High School Diploma or equivalent * Strong data entry and typing skills * Previous experience in a data entry position is preferred * Previous medical or production experience is a plus * Comfortable handling biological specimens * Ability to accurately identify specimens * Experience working in a team environment * High level of attention to detail * Proficient in MS Office * Able to pass a standardized color blind test If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today! Labcorp Is Proud To Be An Equal Opportunity Employer As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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. We encourage all to apply If 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 our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. 254640

At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!Labcorp is seeking a Data Entry Operator to join our team in RTP, NC.Work Schedule: first shift Tuesday-Saturday 9:30am to 6:00pmBenefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.Job Responsibilities * Perform data entry of patient’s results in a timely and accurate manner * Print out and distribute daily worksheets for technical staff * Use various laboratory systems to enter test results * Ensure test results are stored in their proper location * Call client with test results when necessary * Order supplies for the department when need * Other administrative and clericals tasks as required      Job Requirements * High School Diploma or equivalent * Strong data entry and typing skills * Previous experience in a data entry position is preferred * Previous medical or production experience is a plus * Comfortable handling biological specimens * Ability to accurately identify specimens * Experience working in a team environment * High level of attention to detail * Proficient in MS Office * Able to pass a standardized color blind test      If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!Labcorp Is Proud To Be An Equal Opportunity EmployerAs an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.We encourage all to applyIf 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 our accessibility site or contact us at Labcorp Accessibility.For more information about how we collect and store your personal data, please see our Privacy Statement.254640

Data Entry Operator - Labcorp

At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!&lt;br&gt;&lt;br&gt;Labcorp is seeking a Data Entry Operator to join our team in RTP, NC&lt;strong&gt;.&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Work Schedule: first shift Tuesday-Saturday 9:30am to 6:00pm&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Benefits: &lt;/strong&gt;Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN &amp;amp; Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here&lt;strong&gt;. &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Job Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Perform data entry of patient’s results in a timely and accurate manner&lt;/li&gt;&lt;li&gt;Print out and distribute daily worksheets for technical staff&lt;/li&gt;&lt;li&gt;Use various laboratory systems to enter test results&lt;/li&gt;&lt;li&gt;Ensure test results are stored in their proper location&lt;/li&gt;&lt;li&gt;Call client with test results when necessary&lt;/li&gt;&lt;li&gt;Order supplies for the department when need&lt;/li&gt;&lt;li&gt;Other administrative and clericals tasks as required&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Job Requirements&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;High School Diploma or equivalent&lt;/li&gt;&lt;li&gt;Strong data entry and typing skills&lt;/li&gt;&lt;li&gt;Previous experience in a data entry position is preferred&lt;/li&gt;&lt;li&gt;Previous medical or production experience is a plus&lt;/li&gt;&lt;li&gt;Comfortable handling biological specimens&lt;/li&gt;&lt;li&gt;Ability to accurately identify specimens&lt;/li&gt;&lt;li&gt;Experience working in a team environment&lt;/li&gt;&lt;li&gt;High level of attention to detail&lt;/li&gt;&lt;li&gt;Proficient in MS Office&lt;/li&gt;&lt;li&gt;Able to pass a standardized color blind test&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Labcorp Is Proud To Be An Equal Opportunity Employer&lt;br&gt;&lt;br&gt;&lt;/strong&gt;As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.&lt;br&gt;&lt;br&gt;&lt;strong&gt;We encourage all to apply&lt;br&gt;&lt;br&gt;&lt;/strong&gt;If 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 our accessibility site or contact us at Labcorp Accessibility.&lt;br&gt;&lt;br&gt;For more information about how we collect and store your personal data, please see our Privacy Statement.&lt;br&gt;&lt;br&gt;&lt;strong&gt;254640&lt;/strong&gt;

Data Entry Operator

You need a B.S. in Science or Computer Science, 4+ years in software testing, strong documentation skills, and experience with various testing tools and methodologies, preferably in healthcare.

You will manage quality processes, develop test plans and cases, execute tests, report defects, collaborate with teams, and coordinate UAT and demos, preferably in a medical lab setting.

Software Engineering

IT & Cybersecurity

Charlotte

LabCorp is seeking a Software QA Analyst to join the Consumer Genetics IT team. This position is responsible for supporting projects and activities as they relate to IT quality assurance, quality control, quality improvement and UAT support. Job Duties/responsibilities * Quick learner, self-managing with the ability to control the analysis and quality processes throughout the software lifecycle * Ability to project, schedule and track assigned tasks. * Able to determine scope and provide input to manage work effort, project resourcing and risks as required * Develop, review and/or provide inputs into test plans, user acceptance plans, test cases/scenarios, test and traceability matrices, and other quality documents * Perform and/or provide support into the test execution, defect reporting and resolution, user testing/reviews, metrics reporting and status, results validation and documentation storage * Flexible individual, able to collaborate with the development team as well as application support, cross-functional/systems, infrastructure, etc. to ensure the proper implementation of key functionalities, requirements and processes * Work with IT management, product owner and peers in coordinating UAT and functional demos * Experience in a medical reference or genetic laboratory setting preferred Requirements * B.S. Degree in Science or Computer Science or similar discipline * 4+ years of experience in all aspects of software functional testing across a broad set of technologies or healthcare business functional testing or workflow automation experience * Hands-on experience in Test Plan and Test Case development for compliance or validated software systems. * Excellent documentation and communication skills * Experience testing various application types (web based, client/server, COTS, etc.) from a functional and integration perspective * Ability to provide detailed, clear and concise testing documentation to developers / automation engineers / business * Experience using application lifecycle management tools (Team Foundation Server/Azure DevOps, Microsoft Test Manager, JIRA, etc.) * Experience testing or analyzing desktop, Web, middleware components, services and other development technologies * Experience with various lifecycle methodologies: Waterfall, Agile etc. * Strong communication and organizational skills are critical to success among this company of talented individuals * Quick learner who is flexible to work on multiple projects simultaneously * Experience in a medical reference or genetic laboratory setting preferred Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Labcorp Is Proud To Be An Equal Opportunity Employer As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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. We encourage all to apply If 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 our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. 252078

LabCorp is seeking a Software QA Analyst to join the Consumer Genetics IT team. This position is responsible for supporting projects and activities as they relate to IT quality assurance, quality control, quality improvement and UAT support.Job Duties/responsibilities * Quick learner, self-managing with the ability to control the analysis and quality processes throughout the software lifecycle * Ability to project, schedule and track assigned tasks. * Able to determine scope and provide input to manage work effort, project resourcing and risks as required * Develop, review and/or provide inputs into test plans, user acceptance plans, test cases/scenarios, test and traceability matrices, and other quality documents * Perform and/or provide support into the test execution, defect reporting and resolution, user testing/reviews, metrics reporting and status, results validation and documentation storage * Flexible individual, able to collaborate with the development team as well as application support, cross-functional/systems, infrastructure, etc. to ensure the proper implementation of key functionalities, requirements and processes * Work with IT management, product owner and peers in coordinating UAT and functional demos * Experience in a medical reference or genetic laboratory setting preferred      Requirements * B.S. Degree in Science or Computer Science or similar discipline * 4+ years of experience in all aspects of software functional testing across a broad set of technologies or healthcare business functional testing or workflow automation experience * Hands-on experience in Test Plan and Test Case development for compliance or validated software systems. * Excellent documentation and communication skills * Experience testing various application types (web based, client/server, COTS, etc.) from a functional and integration perspective * Ability to provide detailed, clear and concise testing documentation to developers / automation engineers / business * Experience using application lifecycle management tools (Team Foundation Server/Azure DevOps, Microsoft Test Manager, JIRA, etc.) * Experience testing or analyzing desktop, Web, middleware components, services and other development technologies * Experience with various lifecycle methodologies: Waterfall, Agile etc. * Strong communication and organizational skills are critical to success among this company of talented individuals * Quick learner who is flexible to work on multiple projects simultaneously * Experience in a medical reference or genetic laboratory setting preferred      Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.Labcorp Is Proud To Be An Equal Opportunity EmployerAs an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.We encourage all to applyIf 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 our accessibility site or contact us at Labcorp Accessibility.For more information about how we collect and store your personal data, please see our Privacy Statement.252078

Software QA Analyst - Labcorp

LabCorp is seeking a Software QA Analyst to join the Consumer Genetics IT team. This position is responsible for supporting projects and activities as they relate to IT quality assurance, quality control, quality improvement and UAT support.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Duties/responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Quick learner, self-managing with the ability to control the analysis and quality processes throughout the software lifecycle&lt;/li&gt;&lt;li&gt;Ability to project, schedule and track assigned tasks. &lt;/li&gt;&lt;li&gt;Able to determine scope and provide input to manage work effort, project resourcing and risks as required&lt;/li&gt;&lt;li&gt;Develop, review and/or provide inputs into test plans, user acceptance plans, test cases/scenarios, test and traceability matrices, and other quality documents&lt;/li&gt;&lt;li&gt;Perform and/or provide support into the test execution, defect reporting and resolution, user testing/reviews, metrics reporting and status, results validation and documentation storage&lt;/li&gt;&lt;li&gt;Flexible individual, able to collaborate with the development team as well as application support, cross-functional/systems, infrastructure, etc. to ensure the proper implementation of key functionalities, requirements and processes&lt;/li&gt;&lt;li&gt;Work with IT management, product owner and peers in coordinating UAT and functional demos&lt;/li&gt;&lt;li&gt;Experience in a medical reference or genetic laboratory setting preferred&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Requirements&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;B.S. Degree in Science or Computer Science or similar discipline &lt;/li&gt;&lt;li&gt;4+ years of experience in all aspects of software functional testing across a broad set of technologies or healthcare business functional testing or workflow automation experience&lt;/li&gt;&lt;li&gt;Hands-on experience in Test Plan and Test Case development for compliance or validated software systems.&lt;/li&gt;&lt;li&gt;Excellent documentation and communication skills&lt;/li&gt;&lt;li&gt;Experience testing various application types (web based, client/server, COTS, etc.) from a functional and integration perspective&lt;/li&gt;&lt;li&gt;Ability to provide detailed, clear and concise testing documentation to developers / automation engineers / business&lt;/li&gt;&lt;li&gt;Experience using application lifecycle management tools (Team Foundation Server/Azure DevOps, Microsoft Test Manager, JIRA, etc.)&lt;/li&gt;&lt;li&gt;Experience testing or analyzing desktop, Web, middleware components, services and other development technologies&lt;/li&gt;&lt;li&gt;Experience with various lifecycle methodologies: Waterfall, Agile etc.&lt;/li&gt;&lt;li&gt;Strong communication and organizational skills are critical to success among this company of talented individuals&lt;/li&gt;&lt;li&gt;Quick learner who is flexible to work on multiple projects simultaneously &lt;/li&gt;&lt;li&gt;Experience in a medical reference or genetic laboratory setting preferred&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Benefits:&lt;/strong&gt; Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN &amp;amp; Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here&lt;strong&gt;. &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Labcorp Is Proud To Be An Equal Opportunity Employer&lt;br&gt;&lt;br&gt;&lt;/strong&gt;As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.&lt;br&gt;&lt;br&gt;&lt;strong&gt;We encourage all to apply&lt;br&gt;&lt;br&gt;&lt;/strong&gt;If 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 our accessibility site or contact us at Labcorp Accessibility.&lt;br&gt;&lt;br&gt;For more information about how we collect and store your personal data, please see our Privacy Statement.&lt;br&gt;&lt;br&gt;&lt;strong&gt;252078&lt;/strong&gt;

Software QA Analyst

You must have a Ph.D. in chemistry/biochemistry, 3-4 years of relevant experience, fluency in English, method development skills, and knowledge of lab automation and statistics.

You will troubleshoot assays, provide expert guidance on chemistry testing, support staff, manage quality control, assist in vendor relations, and maintain current scientific knowledge.

Science

Research & Development

Geneva

<div>If you are looking for a company where you can gain exposure to a wide variety of science and explore a multitude of career paths across the drug development spectrum, consider working at Labcorp as a Staff Scientist within our Safety Testing department in Geneva.<h2 class="jobSectionHeader">
In more details, you will&hellip;</h2><ul><li>
Perform complex troubleshooting and assist in leading initiatives to solve challenging scientific problems with assays or instrumentation.</li><li>
Apply and interpret scientific theories, concepts, techniques and regulatory requirements in clinical studies and accepts leadership role in developing scientific approaches.</li><li>
Provide expert advice on clinical chemistry testing, including routine chemistry and immunoassays. Support lab and medical staff in test selection and interpretation. Ensure test reports are accurate and complete.</li><li>
Provide consultation to scientific and operational staff on technical issues.</li><li>
Respond to unscheduled deadlines, client needs, crises, etc. without neglecting other duties.</li><li>
Assist with regular monitoring and evaluation of clinical assays to ensure effective scientific performance.</li><li>
May provide technical training for operational staff Provides technical/scientific consultation to departments outside the lab (i.e., Project Management) as requested.</li><li>
Contribute to long-term planning and technical policies of the department.</li><li>
Assist in managing scientific vendor relationships to troubleshoot issues and improve capabilities.</li><li>
Participate in client visits.</li><li>
Regularly read literature related to scientific area of expertise to remain current in knowledge.</li><li>
Manage proficiency testing, quality control, and improvement programs. Identify quality issues and ensure corrective actions are taken.</li><li>
Give presentations to clients and professional groups.</li><li>
Attend meetings, conferences, symposia, and seminars to promote CLS&rsquo;s capabilities within dedicated scientific area.</li></ul><h2 class="jobSectionHeader">
Thrive personally and professionally at Labcorp</h2>
Working at Labcorp, you&rsquo;ll continue to grow in our learning-based culture so you&rsquo;ll know how to expertly respond and adapt as the industry continues to evolve. Here, you&rsquo;ll put your education to work as you play a meaningful role in advancing healthcare and making a difference in people&rsquo;s life.
In addition, Labcorp offers great benefits, global experience and the opportunity to work independently within a team-oriented environment.<h2 class="jobSectionHeader">
What we&rsquo;re looking for</h2>
Staff Scientists are the most successful at Labcorp with:<ul><li>
Ph.D. in chemistry or biochemistry.</li><li>
3-4 years post-doctoral or industry experience within scientific area of expertise (Clinical Chemistry and Immunoassay). Additional relevant experience may be substituted for the education requirements above.</li><li>
Fluency in English, French is a plus.</li><li>
Highly skilled in conducting research, data interpretation, and writing reports.</li><li>
Proven track record of method development.</li><li>
Experience performing scientific presentations and preparing scientific publications.</li><li>
Knowledge of clinical laboratory automation, system software, Microsoft applications and laboratory statistics.</li><li>
Effective communication skills with technical staff, business development staff, peers and clients.</li><li>
Attention to detail and interpretation of scientific data.</li><li>
Demonstrated problem prevention, detection and resolution.</li></ul><h2 class="jobSectionHeader">
Get to know Labcorp</h2>
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.
Here, you can join our more than 60,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people&rsquo;s lives.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.
We encourage all to apply
If 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 our accessibility site or contact us at Labcorp Accessibility.
For more information about how we collect and store your personal data, please see our Privacy Statement.</div>

If you are looking for a company where you can gain exposure to a wide variety of science and explore a multitude of career paths across the drug development spectrum, consider working at Labcorp as a Staff Scientist within our Safety Testing department in Geneva.
In more details, you will…
Perform complex troubleshooting and assist in leading initiatives to solve challenging scientific problems with assays or instrumentation.
Apply and interpret scientific theories, concepts, techniques and regulatory requirements in clinical studies and accepts leadership role in developing scientific approaches.
Provide expert advice on clinical chemistry testing, including routine chemistry and immunoassays. Support lab and medical staff in test selection and interpretation. Ensure test reports are accurate and complete.
Provide consultation to scientific and operational staff on technical issues.
Respond to unscheduled deadlines, client needs, crises, etc. without neglecting other duties.
Assist with regular monitoring and evaluation of clinical assays to ensure effective scientific performance.
May provide technical training for operational staff Provides technical/scientific consultation to departments outside the lab (i.e., Project Management) as requested.
Contribute to long-term planning and technical policies of the department.
Assist in managing scientific vendor relationships to troubleshoot issues and improve capabilities.
Participate in client visits.
Regularly read literature related to scientific area of expertise to remain current in knowledge.
Manage proficiency testing, quality control, and improvement programs. Identify quality issues and ensure corrective actions are taken.
Give presentations to clients and professional groups.
Attend meetings, conferences, symposia, and seminars to promote CLS’s capabilities within dedicated scientific area.
Thrive personally and professionally at Labcorp
Working at Labcorp, you’ll continue to grow in our learning-based culture so you’ll know how to expertly respond and adapt as the industry continues to evolve. Here, you’ll put your education to work as you play a meaningful role in advancing healthcare and making a difference in people’s life.
In addition, Labcorp offers great benefits, global experience and the opportunity to work independently within a team-oriented environment.
What we’re looking for
Staff Scientists are the most successful at Labcorp with:
Ph.D. in chemistry or biochemistry.
3-4 years post-doctoral or industry experience within scientific area of expertise (Clinical Chemistry and Immunoassay). Additional relevant experience may be substituted for the education requirements above.
Fluency in English, French is a plus.
Highly skilled in conducting research, data interpretation, and writing reports.
Proven track record of method development.
Experience performing scientific presentations and preparing scientific publications.
Knowledge of clinical laboratory automation, system software, Microsoft applications and laboratory statistics.
Effective communication skills with technical staff, business development staff, peers and clients.
Attention to detail and interpretation of scientific data.
Demonstrated problem prevention, detection and resolution.
Get to know Labcorp
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.
Here, you can join our more than 60,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.
We encourage all to apply
If 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 our accessibility site or contact us at Labcorp Accessibility.
For more information about how we collect and store your personal data, please see our Privacy Statement.

Staff Scientist - Clinical Chemistry - Labcorp

Staff Scientist - Clinical Chemistry

You need a medical technician CFC, lab experience, document writing skills, IT proficiency, teamwork ability, multitasking, strong communication, and English. IVDR knowledge is a plus.

You will ensure document compliance, conduct clinical tests, manage samples, implement quality control, prepare reports, and maintain instruments while communicating with stakeholders.

<div></div><div><div>Notre Laboratoire Central &agrave; Gen&egrave;ve est &agrave; la recherche d'un(e) Technicien(ne) de Laboratoire /Administrateur(trice) afin de renforcer nos &eacute;quipes en histologie pour une dur&eacute;e de 12 mois.<h2 class="jobSectionHeader">
Sur ce poste, vos responsabilit&eacute;s seront les suivantes:</h2><ul><li>
Assurer la conformit&eacute; des documents avec les normes et les r&eacute;glementations en vigueur.</li><li>
R&eacute;diger et r&eacute;viser la documentation technique au laboratoire en tenant compte des exigences r&eacute;gulatoires.</li><li>
Collecter, classer et compiler des informations provenant de diff&eacute;rentes sources.</li><li>
Assurer la communication r&eacute;guli&egrave;re avec les parties prenantes et les &eacute;quipes.</li><li>
Pr&eacute;parer et pr&eacute;senter des rapports d'avancement lors des r&eacute;unions d&rsquo;&eacute;quipe.</li><li>
Effectuer les tests laboratoires cliniques affect&eacute;s avec pr&eacute;cision, dans le d&eacute;lai imparti.</li><li>
Pr&eacute;parer le poste de travail et l'instrumentation pour les tests affect&eacute;s.
</li><li>Manipuler d&ucirc;ment les &eacute;chantillons, r&eacute;soudre ind&eacute;pendamment les probl&egrave;mes techniques li&eacute;s aux &eacute;chantillons en vue des analyses et du stockage et contacter les clients internes pour clarification selon les besoins.</li><li>
Utiliser les instruments pour ex&eacute;cuter les tests conform&eacute;ment aux proc&eacute;dures &eacute;crites &eacute;tablies.</li><li>
Ex&eacute;cuter des tests et calculs de routine selon les besoins.</li><li>
R&eacute;soudre les probl&egrave;mes d'essais de routine et ceux inhabituels</li><li>
S'assurer de la validit&eacute; des r&eacute;sultats des tests en ex&eacute;cutant des proc&eacute;dures &eacute;tablies d'assurance qualit&eacute; et de contr&ocirc;le qualit&eacute;.</li><li>
Effectuer les exp&eacute;rimentations, selon le calendrier, en vue de l'&eacute;valuation de nouveaux lots &Eacute;talonneur et/ou QC. &Eacute;tablir la synth&egrave;se des r&eacute;sultats des investigations et compiler les donn&eacute;es en vue d'un examen par le management.
</li><li>Documenter les r&eacute;sultats du contr&ocirc;le de la qualit&eacute;, les interpr&egrave;ter conform&eacute;ment aux r&egrave;gles Westgard ou autres proc&eacute;dures de service &eacute;tablies et documenter avec pr&eacute;cision les &eacute;carts, avertissements et violations des valeurs de contr&ocirc;le.
</li><li>Documenter les mesures correctives pour des occurrences inhabituelles (par ex. violations QC, probl&egrave;mes apparent&eacute;s aux instruments).</li><li>
S'assurer que la maintenance des instruments et &eacute;quipements soit ex&eacute;cut&eacute;e conform&eacute;ment aux exigences du fabricant et de la SOP, et document&eacute;e conform&eacute;ment &agrave; la SOP.</li><li>
Comprendre les metrics et les objectifs du service.</li></ul><h2 class="jobSectionHeader">
Education / Qualifications:</h2><ul><li>
Technicien M&eacute;dical titulaire CFC, ou Technicien Biologie Pharmaceutique (titulaire CFC), ou Technicien M&eacute;dical titulaire d'un dipl&ocirc;me de Technologue M&eacute;dical d'une &eacute;cole publique suisse, ou Technicien M&eacute;dical titulaire d'un BTS, DUT, dipl&ocirc;me d'IUT.</li></ul><h2 class="jobSectionHeader">
Experience:</h2><ul><li>
Exp&eacute;rience pr&eacute;alable en laboratoire m&eacute;dical.</li><li>
Exp&eacute;rience dans la r&eacute;daction de documents techniques et r&eacute;glementaires de laboratoire.</li><li>
Ma&icirc;trise des outils informatiques (Word, Excel, logiciels de gestion m&eacute;dicale).</li><li>
Capacit&eacute; &agrave; travailler de mani&egrave;re autonome et en &eacute;quipe.</li><li>
Capacit&eacute; &agrave; g&eacute;rer plusieurs t&acirc;ches simultan&eacute;ment.</li><li>
Excellentes comp&eacute;tences en communication &eacute;crite et orale.</li><li>
Savoir r&eacute;diger des proc&eacute;dures est un plus.</li><li>
Avoir des connaissances sur la r&eacute;gulation IVDR est un plus.</li><li>
Bonne ma&icirc;trise de l&rsquo;anglais.</li></ul></div>
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.
We encourage all to apply
If 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 our accessibility site or contact us at Labcorp Accessibility.
For more information about how we collect and store your personal data, please see our Privacy Statement.</div>

Notre Laboratoire Central à Genève est à la recherche d'un(e) Technicien(ne) de Laboratoire /Administrateur(trice) afin de renforcer nos équipes en histologie pour une durée de 12 mois.
Sur ce poste, vos responsabilités seront les suivantes:
Assurer la conformité des documents avec les normes et les réglementations en vigueur.
Rédiger et réviser la documentation technique au laboratoire en tenant compte des exigences régulatoires.
Collecter, classer et compiler des informations provenant de différentes sources.
Assurer la communication régulière avec les parties prenantes et les équipes.
Préparer et présenter des rapports d'avancement lors des réunions d’équipe.
Effectuer les tests laboratoires cliniques affectés avec précision, dans le délai imparti.
Préparer le poste de travail et l'instrumentation pour les tests affectés.
Manipuler dûment les échantillons, résoudre indépendamment les problèmes techniques liés aux échantillons en vue des analyses et du stockage et contacter les clients internes pour clarification selon les besoins.
Utiliser les instruments pour exécuter les tests conformément aux procédures écrites établies.
Exécuter des tests et calculs de routine selon les besoins.
Résoudre les problèmes d'essais de routine et ceux inhabituels
S'assurer de la validité des résultats des tests en exécutant des procédures établies d'assurance qualité et de contrôle qualité.
Effectuer les expérimentations, selon le calendrier, en vue de l'évaluation de nouveaux lots Étalonneur et/ou QC. Établir la synthèse des résultats des investigations et compiler les données en vue d'un examen par le management.
Documenter les résultats du contrôle de la qualité, les interprèter conformément aux règles Westgard ou autres procédures de service établies et documenter avec précision les écarts, avertissements et violations des valeurs de contrôle.
Documenter les mesures correctives pour des occurrences inhabituelles (par ex. violations QC, problèmes apparentés aux instruments).
S'assurer que la maintenance des instruments et équipements soit exécutée conformément aux exigences du fabricant et de la SOP, et documentée conformément à la SOP.
Comprendre les metrics et les objectifs du service.
Education / Qualifications:
Technicien Médical titulaire CFC, ou Technicien Biologie Pharmaceutique (titulaire CFC), ou Technicien Médical titulaire d'un diplôme de Technologue Médical d'une école publique suisse, ou Technicien Médical titulaire d'un BTS, DUT, diplôme d'IUT.
Experience:
Expérience préalable en laboratoire médical.
Expérience dans la rédaction de documents techniques et réglementaires de laboratoire.
Maîtrise des outils informatiques (Word, Excel, logiciels de gestion médicale).
Capacité à travailler de manière autonome et en équipe.
Capacité à gérer plusieurs tâches simultanément.
Excellentes compétences en communication écrite et orale.
Savoir rédiger des procédures est un plus.
Avoir des connaissances sur la régulation IVDR est un plus.
Bonne maîtrise de l’anglais.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.
We encourage all to apply
If 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 our accessibility site or contact us at Labcorp Accessibility.
For more information about how we collect and store your personal data, please see our Privacy Statement.

Technicien(ne) de Laboratoire / Administrateur(trice) - contrat de 12 mois - Labcorp

Technicien(ne) de Laboratoire / Administrateur(trice) - contrat de 12 mois

You need a CFC in Medical Technology or equivalent, 1 year of FISH cytogenetics experience, and intermediate French language skills.

You will perform FISH techniques, interpret results, maintain equipment, track supplies, collaborate on procedure improvements, and ensure safety standards are met.

<div>Labcorp est une organisation de recherche contractuelle en sciences de la vie d'envergure mondiale qui fournit &agrave; l'industrie pharmaceutique des services d&eacute;di&eacute;s et complets d'essais en laboratoire et de d&eacute;veloppement de m&eacute;dicaments. Nous nous effor&ccedil;ons de faire la diff&eacute;rence dans la vie quotidienne des gens en mettant sur le march&eacute; des m&eacute;dicaments essentiels.
Notre Laboratoire Central &agrave; Gen&egrave;ve est &agrave; la recherche d&rsquo;un(e) Technicien(ne) de Laboratoire en Cytog&eacute;n&eacute;tique FISH afin de renforcer nos &eacute;quipes au sein du d&eacute;partement d&rsquo;Histologie.<h2 class="jobSectionHeader">
Sur ce poste, vos responsabilit&eacute;s seront les suivantes:</h2><ul><li>
Soutenir le d&eacute;veloppement de nouvelles offres de services FISH</li><li>
Effectuer des techniques cytog&eacute;n&eacute;tiques (FISH) semi-automatiques et manuelles.</li><li>
Interpr&eacute;ter les r&eacute;sultats de la FISH sous la supervision du m&eacute;decin responsable.</li><li>
Pr&eacute;parer le poste de travail, l'instrumentation et l'entretien des instruments et/ou de l'&eacute;quipement quotidiennement, hebdomadairement, mensuellement, trimestriellement et annuellement.</li><li>
Aptitude &agrave; tenir des registres pr&eacute;cis et &agrave; respecter les proc&eacute;dures op&eacute;rationnelles standard.</li><li>
Suivi des r&eacute;actifs, du mat&eacute;riel et des fournitures.</li><li>
Collaborer avec les autres membres de l'&eacute;quipe pour am&eacute;liorer les proc&eacute;dures.</li><li>
Respecter les politiques et les normes en mati&egrave;re de s&eacute;curit&eacute; et de sant&eacute; au travail.</li></ul>
Comp&eacute;tences suppl&eacute;mentaires :<ul><li>
D&eacute;calcification de routine, traitement, enrobage, microtomie et r&eacute;-enrobage d'&eacute;chantillons de tissus humains provenant de patients participant &agrave; des essais cliniques.</li><li>
Maintenir des conditions de stockage appropri&eacute;es et la tra&ccedil;abilit&eacute; des blocs et des lames d'histologie (color&eacute;s et non color&eacute;s).</li></ul><h2 class="jobSectionHeader">
Qualifications:</h2><ul><li>
Technicien M&eacute;dical titulaire CFC, ou Technicien Biologie Pharmaceutique (titulaire CFC), ou Technicien M&eacute;dical titulaire d'un dipl&ocirc;me de Technologue M&eacute;dical d'une &eacute;cole publique suisse, ou Technicien M&eacute;dical titulaire d'un BTS, DUT, dipl&ocirc;me d'IUT.</li><li>
Minimum 1 an d'exp&eacute;rience en cytog&eacute;n&eacute;tique (FISH) requise</li><li>
Niveau de langue fran&ccedil;aise interm&eacute;diaire</li></ul>
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.
We encourage all to apply
If 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 our accessibility site or contact us at Labcorp Accessibility.
For more information about how we collect and store your personal data, please see our Privacy Statement.</div>

Labcorp est une organisation de recherche contractuelle en sciences de la vie d'envergure mondiale qui fournit à l'industrie pharmaceutique des services dédiés et complets d'essais en laboratoire et de développement de médicaments. Nous nous efforçons de faire la différence dans la vie quotidienne des gens en mettant sur le marché des médicaments essentiels.
Notre Laboratoire Central à Genève est à la recherche d’un(e) Technicien(ne) de Laboratoire en Cytogénétique FISH afin de renforcer nos équipes au sein du département d’Histologie.
Sur ce poste, vos responsabilités seront les suivantes:
Soutenir le développement de nouvelles offres de services FISH
Effectuer des techniques cytogénétiques (FISH) semi-automatiques et manuelles.
Interpréter les résultats de la FISH sous la supervision du médecin responsable.
Préparer le poste de travail, l'instrumentation et l'entretien des instruments et/ou de l'équipement quotidiennement, hebdomadairement, mensuellement, trimestriellement et annuellement.
Aptitude à tenir des registres précis et à respecter les procédures opérationnelles standard.
Suivi des réactifs, du matériel et des fournitures.
Collaborer avec les autres membres de l'équipe pour améliorer les procédures.
Respecter les politiques et les normes en matière de sécurité et de santé au travail.
Compétences supplémentaires :
Décalcification de routine, traitement, enrobage, microtomie et ré-enrobage d'échantillons de tissus humains provenant de patients participant à des essais cliniques.
Maintenir des conditions de stockage appropriées et la traçabilité des blocs et des lames d'histologie (colorés et non colorés).
Qualifications:
Technicien Médical titulaire CFC, ou Technicien Biologie Pharmaceutique (titulaire CFC), ou Technicien Médical titulaire d'un diplôme de Technologue Médical d'une école publique suisse, ou Technicien Médical titulaire d'un BTS, DUT, diplôme d'IUT.
Minimum 1 an d'expérience en cytogénétique (FISH) requise
Niveau de langue française intermédiaire
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.
We encourage all to apply
If 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 our accessibility site or contact us at Labcorp Accessibility.
For more information about how we collect and store your personal data, please see our Privacy Statement.

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