Senior Scientist: R&D, Assay Development at Kashi Clinical Laboratories
Portland, OR 97219, USA -
Full Time


Start Date

Immediate

Expiry Date

16 Nov, 25

Salary

0.0

Posted On

16 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Life Science Industry, Ngs, Sequencing, Data Analysis, Biochemistry, Experimental Design, Molecular Biology, Assay Development

Industry

Pharmaceuticals

Description

We are searching for a meticulous and dedicated scientist with hands-on laboratory experience in assay development who can work effectively in a fast-paced environment to ensure that the highest-quality clinical assays are developed and launched for our patients.

QUALIFICATIONS

  • Master’s / PhD in molecular biology, biochemistry, or closely related field with at least 4 years experience in assay development for the life science industry
  • Must have hands-on experience with molecular biology techniques, including nucleic acid extraction / quantitation / purification, PCR/qPCR/DDPCR, NGS and Sanger sequencing.
  • Experience in optimizing laboratory methodologies.
  • Demonstrated success in applying independent scientific judgment in experimental design and analysis.
  • Experience in writing clear experimental designs, reports, and operating protocols.
  • Must have excellent communication, organizational, record-keeping, planning, attention to detail, and time management skills.
  • Experience in data analysis

POSITION REQUIREMENTS

  • Duties are performed in the laboratory setting.
  • This position requires the ability to perform repetitive motions during pipetting and samples processing.
  • This position requires the ability to use a computer keyboard, communicate over Zoom/telephone and read printed material.
  • Laboratory activities require periods of standing while working and occasionally lifting heavy objects.

How To Apply:

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Responsibilities
  • Design experimental plans and execute complex end-to-end laboratory experiments.
  • Assay development and validation for commercial launch.
  • Communicate and discuss results with a multidisciplinary group of bioinformaticians, statisticians, and Regulatory Compliance office.
  • Write protocols, document results, make data driven decisions, and present findings at scientific meetings.
  • Develop novel assays and support ongoing work, sample preparation, assay runs, data processing ensuring compliance with current GxP guidance
  • Perform data analysis, critically interpret results, and prepare reports and presentations tailored to the needs and expertise of internal and external stakeholders
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