Senior Scientist # 4874

Responsibilities:

• Independently design, plan, and execute experiments to support platform troubleshooting, optimization, and other research objectives.

• Analyze, interpret, and present experimental results to identify root causes of platform performance issues and provide scientifically sound recommendations.

• Develop, optimize, and troubleshoot experimental methods, protocols, and workflows to improve platform performance, robustness, efficiency, and data quality.

• Investigate technical challenges, identify sources of variability, and implement corrective actions to ensure reliable platform operation.

• Provide day-to-day supervision, coaching, performance feedback, and career development for direct reports.

• Establish team priorities, allocate resources, and ensure timely execution of project deliverables.

• Prepare detailed technical reports, presentations, and documentation summarizing troubleshooting investigations, platform performance, and research findings.

• Collaborate with cross-functional teams to resolve platform-related issues and integrate findings into broader research and development strategies.

• Ensure compliance with laboratory safety, quality, and regulatory standards while maintaining platform reliability and operational excellence.

Required Qualifications:

• PhD in Molecular Biology, Biochemistry, Biotechnology, or related scientific discipline with 2-5 years of relevant research or industry experience; OR Master’s degree with 5-8 years of relevant experience; OR Bachelor’s degree with 8+ years of relevant experience.

• Demonstrated expertise in molecular biology, protein chemistry, or related experimental approaches.

• Proven experience in independently designing and executing experiments from concept to data interpretation.

• Strong track record of technical contributions in research, as evidenced by publications, presentations, or project outcomes.

• Proficiency with relevant laboratory techniques and data analysis tools.

• Effective written and verbal communication skills for technical reports, publications, and presentations.

• Demonstrated level of knowledge regarding applicable regulatory standards commensurate with the position's complexity and scope, contributing to organizational regulatory compliance. Minimal applicable standards for this position include: 

• GMP quality management systems (e.g. ISO 13485)

• Clinical laboratory regulations (e.g. CAP, CLIA, NYSDOH, ISO 15189)

• Operations within the regulated medical device environment (e.g. IVDD, IVDR, FDA 21 CFR 800 series, FDA 21 CFR Part 11)

Preferred Qualifications:

• Advanced technical and analytical skills with the ability to troubleshoot complex scientific problems.

• Strong organizational and project management abilities, including the capacity to prioritize multiple projects.

• Ability to lead and mentor less-experienced team members.

• Collaborative mindset with the ability to work effectively in cross-functional research environments.

• Innovative thinker with the ability to contribute to the development of new technologies and approaches.

Physical Demands and Work Environment

• Work will be performed in an office environment and in a laboratory setting with exposure to biological samples, chemicals, and laboratory equipment.

• Requires consistent use of personal protective equipment (PPE), including lab coats, gloves, and safety glasses.

• May involve extended hours to meet deadlines or conduct time-sensitive experiments.

• Physical requirements include standing for extended periods, pipetting, and handling laboratory equipment and samples.