ELISA Scientist: GMP Biopharma Process Developer

Eurofins; West Point (PA); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions seeks a biologist/chemist to execute and troubleshoot ELISA-based analytical methods for biopharmaceutical process development. The role conducts sample prep, data analysis, and detailed reporting with GMP/GLP adherence, in a cGMP setting at West Point, PA.

The candidate will maintain records, operate with minimal supervision, and continually identify improvements while ensuring safety and regulatory compliance.

Qualifications

• 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.

Responsibilities

• 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.

Skills

ELISA methods

cGMP experience

Microsoft Office

Documentation

Education

Bachelor’s or Master’s in Biology/Biochemistry/Chemistry

Tools

Automated liquid handling systems

Microsoft Office

Job description

Eurofins USA PSS Insourcing Solutions seeks a biologist/chemist to execute and troubleshoot ELISA-based analytical methods for biopharmaceutical process development. The role conducts sample prep, data analysis, and detailed reporting with GMP/GLP adherence, in a cGMP setting at West Point, PA.

The candidate will maintain records, operate with minimal supervision, and continually identify improvements while ensuring safety and regulatory compliance.