Careers

Careers

MPLN offers employment opportunities in diagnostics (molecular, cytogenetics, flow cytometry, anatomic pathology) research and clinical trials, business development, sales, marketing, client services and operations. Located in the foothills of the beautiful Great Smoky Mountains, the laboratory is 20 minutes from Knoxville, Tennessee and offers a flexible benefit package that includes a 401k plan, medical, dental, vision and life insurance, as well as short and long term disability options.

Submit your resumé to the address below or email to .(JavaScript must be enabled to view this email address)

Human Resources
Molecular Pathology Laboratory Network
250 E Broadway
Maryville, TN 37804

Current Positions


Clinical Lab Assistant

Molecular Pathology Laboratory Network, Inc. (MPLN) and its research division Geneuity Clinical Research Services (MPLN/Geneuity) is a privately held College of American Pathologists, New York State Department of Health and ISO15189 accredited laboratory. We offer molecular pathology diagnostic laboratory and contract clinical research services specializing in oncology, infectious disease, women's health, and clinical trials.

Laboratory Assistants/Accessioners are responsible for the proper handling of medical samples in a timely and efficient manner including receiving, entering, verifying, and delivery of specimens. As support personnel, the CLAs are tasked with interfacing with the various testing departments at MPLN to offer effective and timely assistance.

This position's schedule is based on the workload in the department. It is either Monday to Friday or Tuesday to Saturday. All shifts are dayshift.

Essential Functions And Responsibilities

Receive/sign for specimens delivered by couriers.
Sort and unpack specimens based on specific specimen/facility criteria.
Enter specimen data into MPLN's laboratory information system (LIS).
Initiate discrepancy if problems arise with specimen or paperwork accompanying specimen.
Scan paperwork into MPLN's electronic filing system.
Deliver specimens to appropriate departments.
Store specimens based on storage requirements either when a discrepancy has been initiated or the testing department is not able to process sample right away.
Prepare specimens for delivery to outside laboratories.
Participate in the metrology program. Verify the calibration of all applicable instrumentation.
Maintain good working relationship and open lines of communication with medical technologists.
Daily wipe down of work stations and completion of daily quality control logs.
Contact client services as necessary to resolve specimen discrepancies.
Ensure that all orders are correct by reviewing the work of other Accessioners.
Oversee pick up of morning specimens at local UPS when necessary and back up coverage.

Experience and Qualifications

High school diploma or equivalent is mandatory. Associates degree or higher in a science-related field is preferred. Lab experience can substitute for higher education.
Knowledge of specimen processing and tube types is a plus
Must be detail-oriented

Environmental / Working Conditions

Proximity to moving mechanical devices, electrical current, chemicals (toxic, caustic, flammable), fumes, biohazards (contact, airborne, bacterial, and viral), housekeeping cleaning agents including bleach, use of heated devices (hot plates, water baths, steamers).

Physical / Mental Demands

Mobility: Moderate amount of walking, bending, pushing, turning, crawling, stooping and standing. Lifting capability of 25 lbs. Extensive sitting or standing may be required.

Hand Coordination and manipulation: Moderate amount of reaching, grasping, and handling including keyboarding.

Acuity: Color recognition, depth perception and reading are required.

Candidates must be able to pass a pre-employment drug screen and background check.

MPLN is an equal opportunity employer.

Lead Scientist

About Us

Molecular Pathology Laboratory Network, Inc. (MPLN) and its research division Geneuity Clinical Research Services (MPLN/Geneuity) is a privately held College of American Pathologists, New York State Department of Health and ISO15189 accredited laboratory. We offer molecular pathology diagnostic laboratory and contract clinical research services specializing in oncology, infectious disease, women's health, and clinical trials.

With over 30 years of experience in the CAP/CLIA diagnostic laboratory and 15 years supporting oncology clinical trials as a contract research organization, our company is in line for significant, continued growth.

General Summary of Duties

The Lead Scientist position is a cross-disciplinary role at MPLN under the direction and supervision of the Vice President of Scientific Operations and Research. The main duty of the Lead Scientist includes participation in assay development and validation to support MPLN’s research and development (R&D) and clinical trial services. Other responsibilities that may be delegated to the Lead Scientist include performing testing as required to fulfill clinical trial contracts, optimizing workflows across the entire laboratory, training and mentoring new employees, and working closely with the Laboratory Operations and Quality managers to provide oversite for quality assurance and routine laboratory operations.

The Lead Scientist assumes the role of a leadership-level position and will collaborate with the department managers and directors to ensure contracted timelines are met and that quality assurance, testing, and reporting are performed in accordance with the MPLN laboratory requirements. As this position will be 70-80% wet bench work, the Lead Scientist is expected to be 100% on site. The remaining 20% of time will be filled with administrative responsibilities such as report writing, data analysis, and oversite.

Essential Functions, Duties, and Responsibilities

  • Oversees and leads testing of clinical trial specimens in strict accordance with the current study Protocol.
  • Performs troubleshooting of routine laboratory assays and equipment.
  • Contributes to innovation and workflow improvement projects to streamline patient testing.
  • Performs validation and/or verifications of new tests as assigned.
  • Adheres to compliance guidelines (i.e., ISO 15189) as it pertains to the development process.
  • Functions as the primary trainee on new laboratory equipment, specifically that which supports the development pipeline.
  • Functions as the primary trainer to technologists for new assays transferred to operations/production.
  • Provides basic bioinformatics and analytics support in the context of new assay development.
  • Drafts validation plans, validation reports, and standard operating procedures (SOPs) as required for the development pipeline.

Performs other duties, which include, but are not limited to:

  • QA/QC monitoring and reporting according to current MPLN SOPs.
  • Gathers data for quality metrics as assigned.
  • Manage maintenance of assay related equipment.
  • Careful filing/storage of all specimens, papers, test results, and electronic files.

Performs support and educational/training duties.

  • Assists in training and orientation of personnel as assigned by the supervisor.
  • Assists in training and oversite in specific testing areas such as PBMC operations, as assigned.
  • Helps ensure adequate staffing and coverage.

Promotes and maintains positive relationships with all contacts.

  • Facilitates resolution of conflicts and problems as appropriate.
  • Promotes effective interpersonal and interdepartmental relationships.
  • Adopts a team approach to work and acts as a role model providing leadership.
  • Demonstrates the ability to communicate effectively and cooperates with all contacts.
  • Displays patience, tact, a cheerful disposition, and enthusiasm.
  • Willing to work beyond normal working hours, different shifts, or different positions when necessary.

Complies with all MPLN policies and procedures.

  • Complies with conditions of employment as stated in the employee handbook.
  • Helps ensure a safe work environment for all staff.
  • Recognizes incidents and demonstrates the ability to use the NCER system.
  • Educates new staff on reporting procedures and ensures that appropriate forms are completed.

Contributes to the fulfillment of department objectives.

  • Adapts positively to work environment changes.
  • Utilizes work time, equipment, and all supplies in a cost-effective manner.
  • Assists co-workers with job orientation, growth, and development.
  • Oversees and participates in the collection of data for quality performance improvement metrics as requested.

Knowledge, Skills, and Experience Required

Extensive relevant scientific experience is required, including proficiency in data analysis, assay design, and technical writing. Research experience in molecular biology and cell culturing is preferred.

Education, License or Certifications Required

The Lead Scientist must have earned a minimum of a master’s degree in biology, biochemistry, or a life science-related discipline. If clinical testing is required, the Lead Scientist must also hold any relevant certifications and meet continuing education requirements.

Work Environment

The work area is well lit and well ventilated. The potential for exposure to communicable diseases, infectious materials, and potentially harmful chemicals is moderate. Appropriate safety training to mitigate these risks is provided by MPLN.

Physical / Mental Demands

A moderate amount of walking, standing and bending over at desktop and counter-height work surfaces is expected. Sitting for long periods of time may be required, including extended periods working at a computer or reading printed matter. Manual dexterity with both hands is a key demand for effective operation of laboratory instruments and equipment, and for keyboarding. Moderate exposure to musculoskeletal strain may occur from lifting and carrying packages and from reaching above one’s head to place or retrieve stored items. Hearing and vision (aided if necessary) should be within normal ranges.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Some studies will require that operators successfully complete a study-specific qualification protocol that comprises both technical and administrative (organizational) elements: failure to formally ‘qualify’ for a study will preclude participation in those studies.

MPLN is an Equal Opportunity Employer.
Candidates must be able to pass a pre-employment background check and drug test.
Email resumes to HR@MPLNet.com

Software Engineer

Molecular Pathology Laboratory Network, Inc. (MPLN) is seeking a remotely stationed Software Engineer to assist our dynamic team of engineers. They are building a laboratory information management system (LIS or LIMS) for our growing specialty diagnostic and clinical research divisions and for our customers.

Since 1989, Molecular Pathology Laboratory Network, Inc. (MPLN) has been a leader in applying advanced diagnostic laboratory testing in the areas of oncology, infectious disease, genomics and women’s health. Through our clinical divisions (Specialty Anatomic Pathology, Molecular Diagnostics, Flow Cytometry, Cytogenetics and Genomics) and the utilization of automation and a host of advanced molecular technologies, we perform and interpret more than 500,000 specialized tests annually, with specimens emanating from thirty-one states and forty-six countries. For screening, diagnosis, treatment selection and monitoring, MPLN offers a comprehensive portfolio of testing that supports an integrated and seamless diagnostic approach for the evaluation of patients and disease processes.

We are seeking a remotely stationed Full Stack Software Engineer to assist with:

  • Designing, developing, and maintaining both front-end and back-end components for our existing web-based laboratory information system (LIS)
  • Supporting interfaces connecting our LIS with both medical instrument APIs and client systems. Ensuring seamless data flow between laboratory equipment, clients, and the LIS, prioritizing reliability and data accuracy.
  • Conducting software verifications and validations in collaboration with the quality department, adhering to established testing protocols.

Qualifications

  • 3 years of development experience, with a concentration on data-oriented business applications
  • Experience with C# and .NET
  • Familiarity with design/architectural patterns including Model-View-Controller (MVC) and Web API
  • Experience with web development using JavaScript (React and AngularJS preferred)
  • Experience with Node.js frontend toolchains (Yarn, NPM, PNPM, Webpack)
  • Experience with SQL database design concepts and ability to understand and write complex T-SQL queries
  • Experience with SQL Server Reporting Services (SSRS)
  • Bachelor's degree in Computer Science, Software Engineering, or equivalent work experience

This position is an exciting opportunity to be a key player in a growing team. We are looking for the right candidate to grasp a detailed understanding of our business and the various services provided by our laboratory operations and translate those needs into modern software tools.

Candidates must be able to pass a pre-employment background check and drug screen. MPLN is an Equal Opportunity Employer.