About this role
- 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.