ELISA Scientist

Execute and troubleshoot analytical methods, particularly ELISA assays, to support biopharmaceutical process development and process characterization activities. Perform sample preparation, assay execution, data analysis, and technical reporting with a high degree of accuracy and consistency. Apply GMP/GLP principles and maintain the highest quality standards in all laboratory activities. Maintain accurate laboratory records, test results, and technical documentation within approved electronic systems and client-required repositories. Independently perform technical laboratory work with minimal supervision while demonstrating a strong understanding of assay theory, instrumentation, and scientific principles. Perform routine troubleshooting of assays, instrumentation, and laboratory processes by utilizing scientific knowledge, technical resources, and scientific literature to identify and implement effective solutions. Support non-routine experiments and technical studies with a high degree of accuracy, efficiency, and scientific rigor. Identify opportunities to improve laboratory efficiency, productivity, quality systems, and operational processes and assist with implementation of approved improvements. Maintain laboratory organization, inventory control, reagent management, equipment readiness, and supply ordering activities. Independently communicate technical data, experimental findings, project updates, and laboratory issues to peers, management, and client personnel through verbal presentations, technical reports, and professional written communication. Participate in client discussions, technical meetings, and data reviews while communicating scientific concepts effectively to both technical and non-technical audiences. Build and maintain positive client relationships through professional interactions and proactive support of client needs within the scope of the role. Independently manage multiple projects, priorities, and deadlines while maintaining productivity, quality, and attention to detail. Demonstrate accountability, integrity, professionalism, and sound scientific judgment in all work performed while appropriately escalating technical, quality, compliance, or safety concerns. Promote laboratory safety by following all company, client, and regulatory requirements and actively identifying opportunities to improve safety performance and prevent incidents. Conduct all activities in a safe, compliant, and efficient manner while adhering to confidentiality, quality, safety, and client requirements. Perform additional duties, special projects, and cross-functional assignments as required. Bachelor's or Master's Degree in Biology, Biochemistry, Chemistry, or a related scientific discipline. 1-2 years of experience in an analytical, process sciences, process engineering, academic, or industry laboratory environment. Demonstrated experience with ELISA methodologies. Experience working within a cGMP-regulated environment. Proficiency with Microsoft Office applications including Excel, PowerPoint, and Word. Authorization to work in the United States indefinitely without restrictions or sponsorship. Preferred Experience: Experience with automated liquid handling systems. Experience authoring analytical methods, study protocols, or scientific documentation. Prior experience supporting biopharmaceutical development programs. Experience with process characterization studies. The position is Full-Time, on-site, Monday-Friday, 8 a.m.-5 p.m ., with overtime as needed. Candidates currently living within a commutable distance of West Point, PA are encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.