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Scientist II
Job
Planet Pharma Group
Santa Clara, CA (In Person)
$124,800 Salary, Full-Time
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Job Description
Position Summary The Scientist Contractor will be a member of the Assay Development team in Santa Clara for the development of RUO and
CE-IVD/IVD
products for use on next-generation sequencing (NGS) systems. The successful candidate will help develop and implement R D strategies for related NGS applications including nucleic acid extraction, library preparation, sequencing, and data analysis. This position is ideal for individuals interested in continuing their experience in assay and product development, within a design controlled environment.Key Responsibilities:
Laboratory Executions:
- The individual will work under functional manager supervision to plan and conduct hands-on laboratory experiments independently, with high attention to detail. And apply advanced scientific knowledge to complete assigned projects
- Recommend innovative approaches and study plans based on experimental data or new scientific information arising from area of responsibility. Assume responsibility for timely completion of experiments and respond appropriately to changing priorities.
- Designing and performing early development studies, such as optimizations, troubleshooting, reagent selection, assay recommendations, assay characterization.
- Participate in the formulation of reagents, buffers and testing materials following SOP
- Operate automated liquid-handling and sequencing instrumentation.
Data & Documentation:
- Accurately record experimental methods, materials, and results in laboratory notebooks (electronic or paper)
- Analyze data using established tools and summarize findings
- Present findings and/or comprehensive project status reviews at internal and department meetings
- Prepare technical summaries and contribute to verification documentations and reports
- Assist in drafting and revising SOPs and technical documents
- Maintain traceability of materials and documentation within design-controlled processes
- Support documentation requirements for Design History Files (DHF)
Quality & Compliance:
- Perform work in compliance with ISO 13485, QSR, and internal quality systems
- Follow established laboratory safety policies and OSHA guidelines
- Participate in design control documentation activities as assigned
- Ensure accuracy, quality, and timeliness of experimental results
Lab Operations:
- Maintain laboratory equipment and assist with calibration checks
- Manage reagent inventory and ensure proper storage
- Participate in routine lab maintenance and organization
- Support cross-functional teams by providing experimental data as requested Who you are:
- Bachelors degree in Biological Sciences, Molecular Biology, Chemistry, Biochemistry or related field, a Masters or PHD degree is a plus
- Minimum 5 years (with a Bachelors degree, less with advanced degrees) of laboratory experience, or equivalent combination of education and work-related experience
- Strong laboratory proficiency and experience with molecular techniques and concepts, with proficient manual pipetting skills
- Hands-on experience with molecular biology techniques including PCR, qPCR, nucleic acid extraction, and library preparation
- Strong data analysis skills and documentation skills
- Experience in assay design, optimization and validation is preferred.
- Knowledge of NGS based workflows including target enrichment, and library preparation is preferred.
- Strong interpersonal and communication skills.