Scientist, Assay Development

Roche•Carlsbad, NM

1d•Onsite

About The Position

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Roche / GenMark Diagnostics’ mission is to revolutionize patient care by providing high-value, simple-to-perform, and clinically relevant multiplex molecular diagnostics, specifically targeting infectious disease testing. We aim to improve patient outcomes, enhance laboratory efficiency, and reduce total cost-of-care through rapid, sample-to-answer solutions. Roche/GenMark Diagnostics is seeking a Scientist. In this role, the Scientist will demonstrate expertise in advanced nucleic acid amplification technologies. Showing a solid understanding, with hands on experience, in biological sample handling, nucleic acid purification, amplification and detection. In addition, the Scientist will investigate, create, and develop new methods and technologies for project advancement through a combination of individual studies and team research. The Scientist will provide recommendations/observations to scientific staff/management on projects and issues.

Requirements

BS in Biochemistry, Molecular Biology, Analytical Chemistry or a related field with eight or more (8+) years of laboratory experience; OR MS in Biochemistry, Molecular Biology, Analytical Chemistry or a related field with three or more (3+) years of laboratory experience; OR PhD in Biochemistry, Molecular Biology, Analytical Chemistry or a related field with one or more (1+) years of laboratory experience.
Demonstrated experience in molecular diagnostics product development.
Proficiency writing/revising protocols and reports for FDA analytical studies.
Demonstrated mastery in data analysis (including various statistical analyses and DOE), research design, and evaluation of new techniques & procedures for products, systems or technologies.

Nice To Haves

PhD in Biochemistry, Molecular Biology, Analytical Chemistry or a related field.
Knowledge of analytical test methods based CLSI & FDA guidelines.
Excellent organizational skills, including the ability to efficiently evaluate, prioritize and handle multiple changing projects and priorities.
Strong written and verbal communication skills; preparation of documents, including data summaries, reports and procedures.
Demonstrated ability to work collaboratively, fostering professional, constructive relationships as part of a team while also working independently to produce data and meet challenging timelines and goals.

Responsibilities

Analyze and compile experimental data and reports and records results in laboratory notebook.
Prepare documents, including data summaries, reports, SOPs and procedures.
Present work at meetings as required, and propose new strategies and methods to address immediate and upcoming technical issues.
Determine strategic approach to experimental design; integrating results with project and division objectives.
Maintain a high level of expertise through scientific literature, competitor products, and seminars, and serves as technical expert within assay development groups and across other internal departments.
Contribute toward or produce invention disclosures, patents and publications.
Provide work direction and coaching for junior level Research Associates as needed.
Interact with other internal departments, as necessary, to plan and expedite project objectives.