Our client, a world leader in life sciences and biotechnology, is looking for a “Scientist II” based out of Santa Clara, CA.
Job Duration: Long Term Contract (Possibility Of Extension)
PR: $65/Hr on W2 with benefits
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K
We are seeking a Scientist to join the Assay Development team supporting the development of RUO and CE-IVD/IVD products for next-generation sequencing (NGS) platforms. This role will focus on assay development, optimization, validation, and execution of molecular biology workflows within a design-controlled environment.
Key Responsibilities
Design, execute, and troubleshoot laboratory experiments related to NGS assay development.
Perform molecular biology techniques including PCR, qPCR, nucleic acid extraction, target enrichment, and library preparation.
Support assay optimization, characterization, reagent selection, and validation activities.
Operate automated liquid handling systems and sequencing instrumentation.
Analyze experimental data and prepare technical summaries, reports, and presentations.
Maintain accurate laboratory documentation, SOPs, and Design History File (DHF) records.
Support design control, verification, and validation activities in compliance with ISO 13485 and quality system requirements.
Participate in reagent preparation, inventory management, equipment maintenance, and laboratory operations.
Qualifications
Bachelor’s degree in Molecular Biology, Biological Sciences, Biochemistry, Chemistry, or related field; Master’s degree preferred.
5+ years of laboratory experience (less with advanced degree) in molecular biology, assay development, or NGS applications.
Hands-on experience with PCR, qPCR, nucleic acid extraction, library preparation, and NGS workflows.
Experience with assay development, optimization, validation, and troubleshooting.
Familiarity with automated liquid handling platforms (Hamilton, Tecan, Bravo, etc.) and sequencing instruments.
Strong data analysis, documentation, and technical writing skills.
Experience working in regulated environments with ISO 13485, design controls, SOPs, and DHF documentation preferred.
Excellent communication and collaboration skills.
Preferred Skills
Knowledge of NGS target enrichment workflows.
Experience with statistical analysis tools such as JMP, R, or Python.
Prior experience supporting IVD, molecular diagnostics, or genomics product development.
If interested, please send your updated resume to: