Molecular Diagnostics Software and Equipment Specialist

Molecular Software And Equipment Specialist 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 Molecular Software and Equipment Specialist for our lab in Fort Myers, FL 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.

Assist the Molecular Technical Writer in creating and maintaining procedures and other relevant documentation to support laboratory operations changes and maintenance, including technical transfers, assay optimizations, and emerging compliance changes as they pertain to molecular software and equipment Evaluate the feasibility of new instruments and software and provide strategic recommendations for adoption Assist with automation system troubleshooting, maintenance, and optimization to drive continuous improvements Ensure compliance with safety standards and conduct regular audits and quality checks on software and equipment performance Maintain accurate records of equipment quality control activities and collaborate with the Molecular Quality Team to prepare for regulatory audits Act as the primary point of contact for software and equipment-related activities, ensuring accuracy through GDP verifications and facilitating Master Control routing to maintain compliance with regulatory standards Minimal travel required (Up to 10%)Experience, Education and Qualifications :Bachelor's degree in Scientific or Technical Discipline or equivalent work experience required; Master's degree preferred3 or more years of experience in a molecular laboratory, IT, or technical support role required Automation System Certified preferred Certification in Coding Language preferred Demonstrate familiarity with molecular laboratory software, equipment, and automation systems, especially Hamilton Robotics, qPCR instruments, and sequencing instruments Maintain a basic understanding of molecular laboratory and/or analytical techniques Understand CAP/CLIA and FDA (GCP or GLP as appropriate) requirements