Technical Operations Scientist - Oncology Molecular Diagnostics

Are you motivated to participate in a dynamic, multi-tasking environment? Do you want to join a company that invests in its employees? Are you seeking a position where you can use your skills while continuing to be challenged and learn? Then we encourage you to dive deeper into this opportunity.

We believe in career development and empowering our employees. Not only do we provide career coaches internally, but we offer many training opportunities to expand your knowledge base! We have highly competitive benefits with a variety of HMO and PPO options. We have company 401k match along with an Employee Stock Purchase Program. We have tuition reimbursement, leadership development, and even start employees off with 16 days of paid time off plus holidays. We offer wellness courses and have highly engaged employee resource groups. Come join the Neo team and be part of our amazing World Class Culture!

NeoGenomics is looking foraTechnical Operations Scientist(MB ASCP and CGMBS required) who wants to continue to learn in order to allow our company to grow.

Shift time: Dayshift, either Sunday-Thursday or Tuesday-Saturday (subject to change based on business needs)

Now that you know what we're looking for in talent, let us tell you why you'd want to work at NeoGenomics:

As an employer, we promise to provide you with a purpose driven mission in which you have the opportunity to save lives by improving patient care through the exceptional work you perform. Together, we will become the world's leading cancer reference laboratory.

Position Summary:

The Technical Operations Scientist works under general direction and is responsible for conducting scientific and technical development processes leading to the successful completion of company projects including the development of streamlined diagnostic protocols, new methods and automated technology. The Technical Operations Scientist may also serve as the Project Manager and/or Supervisor for assigned projects; where you will supervise project deliverables, manage the sample and data collection process, data monitoring, and all associated project manager tasks.

Core Responsibilities:

• Provides technical guidance, mentors and directs laboratory technologists and associates in performing molecular techniques
• Represents the department in a diverse range of settings, including other groups, clients, audits, vendors, conferences
• Leads technical development projects and executes validation plans
• Trains all levels of staff on new procedures or protocols implemented in the laboratory
• Expedites workflows to maximize capacity by evaluating systems and recommending enhancements; as a team player offers feedback to achieve resolution of production problems/issues involving other departments
• Works closely with management in the monitoring and correction of trends and problems in equipment operation, reagent usage and test procedures performance
• Serves as a technical resource for the department by investigating and resolving analytical testing problems, recommending a course of action in instances identified as beyond acceptable limits, and responding to non-routine/complex inquires and/or requests from clients and sales representatives
• Drives all aspects of the project management process from initiation, planning, execution, control and closure
• Responsible for building and maintaining project timelines for each project, and uses these timelines to track and handle a project’s progress
• Responsible for periodic (weekly, or as needed) product development team meetings
• Reviews study metrics for performance and quality with the team and management
• Works with external and internal teams to ensure that sample acquisition; data collection and distribution of samples to the teams support the R&D and Clinical activities and deliverables
• Travel: ~25% (1-2 days/week) or as needed, project dependent

Experience, Education and Qualifications:

• Bachelor’s Degree in a scientific discipline required. Master’s preferred.
• Six or more years of equivalent experience (high complexity testing) preferred
• Familiarity with CAP/CLIA and FDA (GCP or GLP as appropriate) requirements and knowledgeable with the specialty requirements within those organizations
• Deep understanding of laboratory and/or analytical techniques
• Nationally: ASCP certification for the assigned specialty, as available
• CA: Current state license to perform laboratory testing