In this role, the Technical Supervisor will be responsible for assisting in all facets within the laboratory to include develop budget, timelines, milestones, and assess anticipated regulatory hurdles as well as overseeing conduct and safety. This position requires extensive hands-on experience with Enzyme-Linked Immunosorbent Assay (ELISA) testing for qualitative analysis and Liquid Chromatography-Mass Spectrometry/Mass Spectrometry (LC-MS/MS) testing for the identification and quantitation of analytes in question. The role requires excellent systematic troubleshooting skills with ability to handle problems independently and implement corrective action, perform preventative maintenance and repairs, data analysis, data reporting and calibration on laboratory analytical equipment.Additionally, this position requires the ability to be mechanically inclined and detail oriented.
The position requires processing of the LC-MS/MS data using sophisticated software tools, evaluation and interpretation of the collected data. The individual would also be expected to prepare and report technical data accurately, as well as provide conclusions and recommendations based on the data collected. This position assumes departmental responsibility for discovery or development projects, if needed. The individual performs all work in conformance with applicable regulations. The individual also performs all work in a safe manner.
As an employee, you will actively contribute to the discovery, development of our methods, which in turn, delivers to our patients and customers. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect SteelFusion Clinical Toxicology Laboratory, LLC’s high regard for our employees. Skip t Main Content
Strong critical thinking, excellent communication and problem solving skills;
Ability to develop and follow research methodology and protocols;
Knowledge of current technological developments/trends in area of expertise;
Ability to read, understand, follow and enforce safety procedures;
Ability to design, organize and coordinate scientific research projects;
Highly desirable experience includes the use of Agilent Technologies Triple Quadrupole LC-MS/MS method development and ELISA testing;
ELISA and LC-MS/MS instrument maintenance and troubleshooting experience;
Plan and conduct scientific/laboratory experiments and evaluate and interpret data;
Provide training and guidance to laboratory personnel;
Prepare technical reports, publications and oral presentations, if applicable;
Act as a leader in absence of supervisor;
Appropriate level of understanding of applicable regulations;
Responsible for participating in the update and development of analytical procedures, QC procedures, and SOPs;