As an ELISA Scientist I/II, you will be responsible for developing, establishing, validating, and executing bioanalytical methods used to support biopharmaceutical testing. This role requires strong laboratory skills, data analysis capabilities, and a commitment to scientific excellence and regulatory compliance.
The ideal candidate has hands-on experience with immunoassays and enjoys working in a collaborative, fast-paced laboratory setting where quality, accuracy, and client service are top priorities.
Key Responsibilities
• Perform and support method development, establishment, transfer, and validation activities for ELISA and multiplex ELISA assays.
• Execute bioanalytical testing using electrochemiluminescence (ECL) platforms and other immunoassay technologies.
• Generate, analyze, interpret, and review scientific data to ensure accuracy and compliance with cGMP requirements.
• Utilize software platforms such as SoftMax Pro and laboratory systems to process and evaluate assay results.
• Troubleshoot assay performance and identify opportunities for continuous improvement.
• Prepare technical documentation, protocols, reports, and validation summaries.
• Train and mentor laboratory personnel on established methods and best laboratory practices.
• Maintain accurate records in accordance with SOPs, regulatory requirements, and data integrity standards.
• Work effectively within a Laboratory Information Management System (LIMS).
• Collaborate with cross-functional teams to ensure projects are completed on schedule and meet client expectations.
• Support laboratory operations while maintaining a safe, organized, and compliant work environment.
Minimum Qualifications
• Bachelor's degree in Biology, Biochemistry, Biotechnology, Cell Biology, Immunology, or a related scientific discipline.
• 0-4+ years of relevant academic or industry laboratory experience.
• Authorization to work in the United States without current or future sponsorship.
Preferred Qualifications
• Experience performing ELISA, multiplex ELISA, MSD, or other ligand-binding assays.
• Knowledge of bioassay development, qualification, and validation.
• Familiarity with cGMP, GLP, or other regulated laboratory environments.
• Experience supporting biologics, therapeutic proteins, antibodies, vaccines, or cell- and immuno-based assays.
• Proficiency with laboratory data analysis software and Microsoft Office applications.
• Excellent organizational, problem-solving, and communication skills.
• Ability to manage multiple priorities while maintaining a high level of accuracy and attention to detail.
Schedule
Full-time | Monday-Friday | 8:00 AM-4:30 PM
Additional hours may be required based on project and client needs.
Benefits
Eurofins offers a comprehensive benefits package, including:
• Medical, dental, and vision coverage
• Company-paid life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Employee assistance programs
• Career development and advancement opportunities
Candidates living within a commutable distance of Columbia, MO are encouraged to apply.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.