Analytical Clinical Biochemist

Eurofins•Rensselaer, NY

7d•$21 - $24

About The Position

Join our dynamic laboratory team supporting critical pharmaceutical clinical testing. We are seeking a detail‑oriented and motivated Biochemistry Laboratory Associate who thrives in a regulated environment, enjoys hands‑on bench work, and values accuracy, collaboration, and continuous learning. Key Responsibilities Perform data collection and accurately document test results. Follow established standard operating procedures (SOPs) to complete daily laboratory tasks. Review test data for compliance with quality standards; promptly report any anomalies. Comply with all applicable regulatory and agency requirements. Operate within a GMP‑regulated lab supporting clinical testing. Participate in required training and maintain competency in assigned tasks. Maintain laboratory supplies and support inventory control. Complete test records and perform routine data review with high accuracy. Follow Good Documentation Practices (GDP) in both paper and electronic record systems. Calibrate or verify calibration of instruments and equipment prior to use. Communicate effectively with internal teams and external partners as needed. Assist with method validation activities when required. Demonstrate strong scientific, computer, and organizational skills. Work both independently and collaboratively, showing adaptability, initiative, and a positive attitude. Learn new techniques efficiently, manage multiple tasks, maintain precise records, and adhere to company policies.

Requirements

Bachelor’s degree in biochemistry or another science‑related field, and 0-2 years of directly related industry experience
Authorization to work in the United States indefinitely without restriction or sponsorship.
Experience with biochemistry assays and techniques, including but not limited to:
Experience with ELISAs
Working with 96-well plates
Serial dilutions
Working with small volumes with multi-channel pipette
Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

Perform data collection and accurately document test results.
Follow established standard operating procedures (SOPs) to complete daily laboratory tasks.
Review test data for compliance with quality standards; promptly report any anomalies.
Comply with all applicable regulatory and agency requirements.
Operate within a GMP‑regulated lab supporting clinical testing.
Participate in required training and maintain competency in assigned tasks.
Maintain laboratory supplies and support inventory control.
Complete test records and perform routine data review with high accuracy.
Follow Good Documentation Practices (GDP) in both paper and electronic record systems.
Calibrate or verify calibration of instruments and equipment prior to use.
Communicate effectively with internal teams and external partners as needed.
Assist with method validation activities when required.
Demonstrate strong scientific, computer, and organizational skills.
Work both independently and collaboratively, showing adaptability, initiative, and a positive attitude.
Learn new techniques efficiently, manage multiple tasks, maintain precise records, and adhere to company policies.