Scientific Technical Writer - NeoGenomics Laboratories

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 for a Scientific Technical Writer who wants to continue to learn in order to allow our company to grow.

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 Scientific Technical Writer is an integral part of the Molecular team at NeoGenomics. The Technical Writer will be supporting the Technical Operations Scientists in the transfer and optimization of new and existing products into the department or site. The Technical Writer is needed to support documentation efforts within the Molecular team in order to ensure Laboratory Operations is running smoothly and business needs are met. This role also requires collaboration with several groups at NeoGenomics including R&D, QA, Medical and other cross-functional teams as needed.

Core Responsibilities:

• The role will assist in creating and maintaining procedures and other relevant documentation to support Laboratory Operations changes, including technical transfers and assay optimizations
• Meet with subject-matter experts and analyze information required for the development of testing plans and reports
• Collaborate with R&D, Lab Operations, and QA, as necessary for documentation drafting
• The role will provide support and training to staff members as necessary.
• Exhibit strong organizational and time management skills and be able to work on multiple tasks/projects simultaneously
• Travel: up to 10%

Requirements:

• A Bachelor’s (BS) in molecular biology, biochemistry, engineering, or related field
• A minimum of 2 years working experience in high-throughput complex diagnostic workflows, preferably NGS-based assays
• Minimum of two years of experience as a Medical Technologist / Licensure as CLS preferred
• Experience in working in a CLIA/CAP lab, preferably in an FDA-regulated environment for IVD under design control
• Experiencing authoring and preparing validation plans, reports, and Work Instructions/SOP’s.