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Scientist II

Iconma

Santa Clara, CA

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JOB DETAILS
SALARY
$39.46–$67.20 Per Hour
SKILLS
Assay Development, Assays, Biochemistry, Biology, Biotech and Pharmaceutical, Calibration, Chemistry, Communication Skills, Cross-Functional, Data Analysis, Detail Oriented, Document Management, Documentation, Equipment Maintenance/Repair, Health Plan, ISO (International Organization for Standardization), Identify Issues, Instrumentation, Interpersonal Skills, Inventory Management, Laboratory, Laboratory Equipment, Laboratory Notebook, Laboratory Operations, Materials Testing, Molecular Biology, Next Generation Sequencing (NGS), Nucleic Acid, OSHA, Policy Development, Polymerase Chain Reaction (PCR), Product Development, Quality System Requirements (QSR), Real-time PCR (qPCR), Record Keeping, Research & Development (R&D), Standard Operating Procedures (SOP), Team Player, Technical Writing, Time Management, Traceability
LOCATION
Santa Clara, CA
POSTED
1 day ago
Our client, a Biotech company, is looking for a Scientist II for their Santa Clara, CA location.
 
Responsibilities:
  • 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.
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
 
Requirements:
  • 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.
 
Why Should You Apply?

About the Company

I

Iconma

ICONMA is a global information consulting management firm providing Professional Staffing Services and Project-Based Solutions for organizations in a broad range of industries.

  • Corporate Headquarters in Troy, Michigan; 20+ locations worldwide.
  • Certified Woman-Owned Business Enterprise (WBE); certified by Women’s Business Enterprise National Council, National Women Business Owners Corporation (NWBOC); and California Public Utilities Commission (CPUC).
  • Founded in 2000
  • 2000+ Employees

The company was founded on the principle that success is derived from delivering high quality service and resources in the most responsive, flexible, and innovative way. ICONMA invests in people and resources with a single goal: To provide our customers with the highest quality service in the most responsive manner. Through its network of offices, ICONMA provides the resources to help clients maintain their competitive advantage.

COMPANY SIZE
2,000 to 2,499 employees
INDUSTRY
Management Consulting Services
EMPLOYEE BENEFITS
401K, Employee Referral Program, Life Insurance
FOUNDED
2000
WEBSITE
https://www.iconma.com/