Validation Specialist, Flow Cytometry

Labcorp • Brentwood, TN

3d

About The Position

At Labcorp, we believe in the power of science to change lives. We are nearly 70,000 people across 100 countries who are harnessing science for human good. Our work combines unparalleled diagnostic laboratories, drug development capabilities and commercial innovations. Together, we fuel scientific breakthroughs and deliver more than 160 million medical test results that help guide treatment decisions, accelerate patient care and change lives. Join us in our pursuit of answers. What to Expect... 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.

Requirements

• 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.
• Minimum of a Bachelor's degree in Biology or related field.

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: Mid Level
• Number of Employees: 5,001-10,000 employees