Scientist II

Role: Scientist II (Contract W2 Role)

Location: Santa Clara, CA

Interview process: 1. phone 2. Virtual or in-person

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:

• Bachelor's degree in Biological Sciences, Molecular Biology, Chemistry, Biochemistry
  or related field, a Master's or PHD degree is a plus
• Minimum 5 years (with a Bachelor's 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. Ability to work in a team
  environment.

Thank You

vinaya@itengagements.com