Research Associate II, OEM/Special Projects

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 inventory, monitor reagent supplies, and support procurement activities through ERP systems such as SAP
Adhere to company Personal Protection Equipment (PPE) policy
Perform other duties as required, or assigned by management, to meet business needs
Master's degree in Biochemistry, Molecular Biology, Biotechnology, Biological Sciences, or a related scientific discipline with no prior experience required; OR Bachelor's degree in Biochemistry, Molecular Biology, Biotechnology, Biological Sciences, or a related scientific discipline with relevant laboratory experience
Experience in Molecular Biology related activities such DNA/RNA Purification, PCR (endpoint, real time PCR or digital PCR), DNA/RNA electrophoresis and DNA/RNA processing and/or modifications
First-hand experience with aseptic techniques
Proficient with Microsoft Office, particularly Outlook, Word, Excel, and PowerPoint
Demonstrated communication skills, with the ability to communicate in various formats to internal teams
Desired Knowledge and Qualifications:
3+ years of relevant laboratory experience
Experience working on third party customer product development and manufacturing
Experience with mammalian cell culture and viral cultures
Experience guiding or training research associates on established procedures
Experience in performing data interpretation/analysis after project execution for team review
Proficiency in ERP systems such as IFS, SAP, or Microsoft Dynamics
Experience handling products under ISO13485 quality management system
Experience working in GMP environment, following SOPs, generating customer facing documents and documentation for QA review and approval
Behavioural and Interpersonal Competencies:
Resonate and operate in line with LGC’s core value behaviors: Passion, Curiosity, Integrity, Brilliance, and Respect
Ability to work well in a team environment, willingness to adapt to changes and a proven ability to exert influence in a directive and positive manner
Ability to work collaboratively in a cross-functional team environment
Demonstrated autonomy: ability to self-start and drive while recognizing the appropriate time for stakeholder engagement
Adaptable and willing to take on multiple new tasks and responsibilities while managing and prioritizing multiple tasks within a dynamic work environment
Ability to perform preliminary data interpretation and analysis and communicate results effectively
Strong organizational, planning, and documentation skills
Ability to prioritize multiple projects and meet established timelines
Strong problem-solving and troubleshooting abilities
Commitment to maintaining laboratory safety, quality, and regulatory compliance standards

Employment type
Full-time

Work arrangement
No