Research Technician I

Research Technician I

The Research Technician is primarily responsible for performing laboratory tests and analyses under the direction of a lab manager or research scientist. Duties include, but are not limited to, specimen management, specimen pipetting, instrument operation/maintenance, data entry, specimen storage, following Standard Operating Procedures (SOPs) and ensuring all laboratory equipment and work areas are clean, sterile, and in proper working order. Applicant may be responsible for calibration of instruments and conducts routine tasks as directed. Works under moderate supervision with some latitude for independent judgment.

Research Technician responsibilities include, but are not limited to, the following :

• Perform sample preparation steps which may include specimen pipetting with a high degree of accuracy and precision
• Provide support as an instrument operator to both BioPharma and Clinical projects
• Execute supervised experiments adhering to protocols.
• Perform reagent and material preparation for testing
• Maintain adequate inventory of supplies, reagents and materials needed for testing
• Document remedial action, troubleshooting, quality assurance activities and instrument maintenance
• Adhere to established processing timelines
• Perform data queries of the Laboratory Information Management System (LIMS)
• Backup to Research Lab Assistant as volume / need requires. For example:
• Custom labelling of samples
• Retrieve and catalog samples for testing
• Properly store specimens for short term and long term storage
• Perform cleaning and maintenance duties for laboratory spaces and instrumentation
• Accurately prepare, label and store reagents, standards, controls and patient specimens for analytical, clinical and biopharma validations analysis and short and long-term storage
• Calibrate and maintain all assigned laboratory equipment and instruments according to standard operating procedures to ensure quality results
• Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies
• Operate all laboratory equipment and instruments according to standard operating procedures to ensure quality results
• Adhere to policies and protocols in the lab
• Disposes of bio hazardous materials, chemical waste, sharp and other potentially hazardous materials according to regulations
• Review daily run documentation for completeness and accuracy with provided reviewer guidelines.
• Keep accurate documentation of all research project steps according to Viracor BioPharma Eurofins regulatory guidelines
• Work closely and communicate with other lab associates to complete daily activities efficiently

The ideal candidate would possess :

• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

Basic Minimum Qualifications :

• Bachelor's degree in chemistry, biology, biochemistry, or other related degree concentration, or equivalent directly-related experience (At least six months related experience from internship, independent research, or industry laboratory)
• Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

• Positions is, Monday-Friday, 8 a.m.-5 p.m.. Candidates currently living within a commutable distance of Lenexa KS are encouraged to apply.

Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.