Job Details

ID #12376073
State Texas
City Cedarcreek
Job type Contract
Salary USD Depends on Experience Depends on Experience
Source NetSource, Inc.
Showed 2021-04-18
Date 2021-04-16
Deadline 2021-06-15
Category Et cetera
Create resume

Molecular Biologist

Texas, Cedarcreek, 78612 Cedarcreek USA

Vacancy expired!

Please note that this is a 1 year contract position. The client is seeking a highly motivated individual to support Genomics R&D organization. This is a hands-on position developing and verifying performance of IVD or environmental screening products. In this position, you will help bring new molecular diagnostic or screening tests to market.Responsibilities:The primary role will be to perform wet lab bench experiments, both independently and as directed by Senior Scientists, primarily focusing on development and validation of QPCR/QRT-PCR and nucleic acid extraction methods, including processing potentially-infectious clinical or environmental specimensCollect, analyze, and document primary data from experiments, troubleshoot technical issues, and plan next steps to meet objectives outlined by the project teamEffectively communicate scientific results in both written format and orally at group meetings, including with colleagues at remote sitesAssist senior scientists with lab maintenance, supply, and organizational tasks to ensure compliance with regulatory and quality standardsEfficiently manage workload to quickly and accurately execute experiments and meet aggressive deadlinesMeticulously document experiments and verification/validation (V&V) studies in the Electronic Laboratory NotebookEnsure all aspects of V&V studies are conducted according to internal and external quality and regulatory requirementQualifications:BS or MS in Molecular Biology or related life science fieldAt least 3-5 years of hands-on laboratory experience with QPCR/QRT-PCR, nucleic acid extraction from clinical or environmental specimens, and related molecular diagnostic techniques; experience processing challenging sample matrices is a plus.Experience supporting regulated products and adhering to strict quality and regulatory requirements; prior experience working in a CLIA/CAP environment is a plusExperience operating in a high-throughput, high-complexity lab, with both manual and automated sample processing equipment, under high deadline pressureExperience with method development of molecular diagnostic procedures is a plusDemonstrated technical writing and oral communication skillsDemonstrated proficiency with standard scientific analysis software and toolsApplicants must provide their phone number. Reference job number A766.

Vacancy expired!

Subscribe Report job