This full-time position will have primary responsibilities to plan and execute projects in the Applied Research and Technology and Product Development teams. Projects will include transfer of product concepts from the internal research teams or external technology partners with a strong focus on mass spectrometry and proteomic analysis. Candidates with prior experience with mass spectrometry methods are highly desired for this role. The research associate may expand their contributions to our cellular, PCR, and NGS testing modalities over time. Additional responsibilities include in the development of concepts to transfer and launch implementation in collaboration with our Product Development and Laboratory Operations team.
The ideal candidate is team oriented, technically sound, driven to execute, and very attentive to project goals. This candidate will also be attentive to the project aims, able to read and comprehend peer-reviewed published literature, collaborate with colleagues internally and externally on focused projects and document plans and results within notebooks and in formal documents within the QMS. Advancement is dependent on the ability to work with decreasing levels of supervision as well as recognized delivery in compliance with the Product Development Policy and Process.
Responsibilities include assisting with applied research and development including ongoing daily management and performance of established laboratory test processes, as well as ensuring on-going compliance with all federal, state, and local regulations which govern the operation of the laboratories. This position will be required to gain and maintain competence in the Laboratory Operations testing procedures, routinely execute at the bench including processing of human blood, tissue and cell samples in a high complexity testing Laboratory.
In summary, the candidate will have a strong scientific and technical background in mass spectrometry, including trouble-shooting experiences, be competent with the peer-reviewed literature, conducting independent data analyses, be compliant with Good Laboratory Practices (GLP) including with documentation, competent in developing plans and reports in our Quality Management System and deliver technical presentations on projects.
Ongoing training will be provided to supplement key skills required to perform the functions of this position as applicable.