Product Development Research Associate
6 months ago
Would you like to join an innovative team driven by a bold vision - _unleashing tools to accelerate breakthroughs in human health?_
It is an extraordinary time for Standard BioTools. Our technology is empowering customers to improve life through comprehensive health insight. We invite you to join a leading provider of indispensable life sciences tools that is accelerating global research on multiple frontiers of human health.
At Standard BioTools, we are building a positive culture where our people can do the best work of their careers, informed, and influenced by our core behaviors:
- Keep customers front and center in all our work
- Be accountable and deliver on commitments
- Drive continuous improvement
- Be collaborative and work as one team: fostering communications in a
learning, coaching, and helpful environment
Description:
- Develop an advanced understanding of the suspension mass cytometry platform.- Support product development scientists to develop and test new and existing products.- Execute laboratory experiments using the suspension mass cytometry platform for product development.- Possess attention to detail and understanding of the process in the execution of scientific methods.- Maintain records to ensure a laboratory environment that complies with regulatory requirements (eg. ISO 13485), good laboratory practices, and standard operating procedures.- Perform data analysis, prepare technical reports and present at technical reviews, as required.- Support laboratory operations that relate to reagent product development.
Minimum Qualifications:
- A degree in life sciences, such as immunology; MSc is preferred.- Experience in flow cytometry and/or mass cytometry workflows (e.g. sample prep, cell staining, sample acquisition, antibody conjugation) is an asset. A minimum of 2 years experience in flow cytometry and/or mass cytometry is desirable.-
- Ability to read, analyze, and interpret scientific and technical reports, technical procedures, validation protocols and reports, operating instructions, and scientific publications.- Familiarity with Design Control, ISO13485 and/or regulatory environment is an asset.- Excellent organizational and communication skills to enable multi-tasking.- Attention to detail is essential.- Excellent problem solving and interpersonal skills.- Collaborative attitude within and outside own discipline.- Ability to relocate to the Greater Toronto Area in Ontario, Canada.
Ready to join an industry leader with a bold and ambitious mission that is enabling advancements in human health?
- Standard BioTools _is committed to providing an inclusive and barrier free recruitment process to applicants with accessibility needs in accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act (AODA). If you require an accommodation during this process, please inform Standard BioTools of your requirements. We are an equal opportunity employer._
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