Validation Specialist, Flow Cytometry

Labcorp • Brentwood, TN

1d

About The Position

Labcorp is seeking a Validation Specialist to join our Flow Cytometry team in Brentwood, Tennessee! Job Responsibilities: Specialist will be responsible for achieving all of the deliverables expected in a validation project within a reasonable timeline as assigned by Supervisor and Scientist. This will include performing tasks like planning, documenting, performing bench work, analysis of data, and reporting of data to management. The Specialist shall maintain, QC, acquire specimens, and perform some troubleshooting on sophisticated flow cytometers and other lab equipment. The Specialist is responsible for alerting management to instrument issues and may be required to request instrument service from appropriate vendor. Excellent written skills are required for the generation of validation plans/reports and SOPs with supervision from management. The statements herein reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job. It is the responsibility of all employees to comply with all applicable regulations e.g. Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Good Laboratory Practice (GLP) in the performance of their role. Minimum Qualifications: Bachelor’s degree in Biology or related field. Individual must have some laboratory experience that includes pipetting. Strong computer skills and experience with Microsoft Excel and Word are required. Additional Job Standards: Excellent verbal and written skills. At Labcorp we have a passion for 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! 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: Labcorp 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. 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. We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.

Requirements

• Bachelor’s degree in Biology or related field
• Individual must have some laboratory experience that includes pipetting
• Strong computer skills and experience with Microsoft Excel and Word are required
• Excellent verbal and written skills

Responsibilities

• achieving all of the deliverables expected in a validation project within a reasonable timeline as assigned by Supervisor and Scientist
• performing tasks like planning, documenting, performing bench work, analysis of data, and reporting of data to management
• maintain, QC, acquire specimens, and perform some troubleshooting on sophisticated flow cytometers and other lab equipment
• alerting management to instrument issues and may be required to request instrument service from appropriate vendor
• generation of validation plans/reports and SOPs with supervision from management
• comply with all applicable regulations e.g. Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Good Laboratory Practice (GLP) in the performance of their role

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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level