Research Associate II, OEM​/Special Projects

• Full-time
• Work Arrangement:
  On-site
• Department:
  Scientific / Technical Science

LGC's Clinical Diagnostics Division develops and manufactures a comprehensive portfolio of catalog and custom-developed diagnostic quality solutions and component materials for the extended life sciences industry. We partner with IVD assay developers, and pharmaceutical, CRO and academic institutions in commercialization activities across the entire diagnostic pipeline - from concept and early stage research, through expedited product development and onwards into routine clinical use.

Laboratorians and diagnostic professionals across disciplines of clinical chemistry, immunochemistry, serology, molecular diagnostics and clinical genomics rely on LGC's products to support accurate and reliable diagnostic results.
Our operating entities include Sera Care Life Sciences and Maine Standards Company, which are in vitro diagnostics (IVD) manufacturers of quality measurement tools (calibrators, controls, linearity, EQA/PT, biological materials) and the Native Antigen Company, which is a manufacturer and supplier of viral antigens. Our 300+ employees operate FDA-registered and ISO 13485-accredited facilities in Maine, Massachusetts and Maryland, USA, and an ISO 9001-accredited facility in Oxford, UK.
Each day, our world-class staff, scientific expertise, operational efficiency and superior quality systems are ready to support the range of advanced technologies that collectively improve patient outcomes - from the widely adopted and established through to cutting-edge NGS and precision diagnostics.

The Research Associate II, OEM/Special Projects supports the research, development, verification, and optimization of molecular diagnostic products, reagents, and associated processes. This role independently performs routine and non-routine laboratory procedures utilizing cellular and molecular biology techniques to quantify, characterize, and manipulate genetic material. The position is responsible for executing assigned experiments, maintaining accurate documentation, analyzing experimental data, and contributing to project objectives within established timelines.

The Research Associate II works with moderate supervision, applies scientific knowledge to troubleshoot routine technical challenges, and collaborates effectively with cross-functional teams to support product development activities.

To perform this job successfully, an individual must be able to capably perform each of the following essential duties:

• Perform general molecular techniques such as nucleic acid purification, gel-electrophoresis, RNA transcription, cell culture, and bacterial culture
• Perform nucleic acid analysis (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results
• Culture cells using aseptic techniques and downstream processing of cultured cells
• Manufacture product following standard operating procedures and work instructions provided
• Organize projects and data using Excel, Word, PowerPoint, and a document control system (EtQ)
• Work with supervisor to plan and execute experiments and tasks as assigned according to the timelines and ensure documentation meets GLP/GMP requirements
• Record test results and data records, seek appropriate approval and file according to established procedures
• Maintain, calibrate, and operate equipment according to established protocols. Monitor equipment for appropriate operation within set parameters and refer abnormal results to lab management
• Plan for raw material requirements by maintaining appropriate inventory of reagents and ordering reagents as needed through an ERP system (SAP)
• Collaborate with cross-functional teams to complete assigned custom project related activities
• Maintain a clean, organized, and safe laboratory environment while adhering to applicable safety and quality requirements
• Contribute to continuous improvement initiatives by identifying opportunities to improve laboratory processes, efficiency, and data quality
• Accurately document laboratory activities, test results, observations, and data in laboratory notebooks and electronic systems in compliance with applicable quality standards and regulatory requirements
• Identify and communicate routine technical issues, recommend solutions, and assist with implementing corrective actions
• Assist in the development, revision, and review of standard operating procedures (SOPs), work instructions, and technical documentation
• Manage laboratory…