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Dawar Consulting, Inc.

Dawar Consulting, Inc.

Research Associate I - Assay Development/Wet Laboratory

Tucson, USNa miejscuUmowaPełny etat

Opublikowano 23 wrz 2026

To stanowisko jest opublikowane w języku EN

Our client, a world leader in life sciences and biotechnology, is looking for a “Research Associate I” based in Tucson, AZ.


Job Duration: Long Term Contract (Possibility Of Extension)

Pay Rate : $27/hr on W2


Company Benefits: Medical, Paid Sick leave, 401K


Entry-level Research Associate supporting early-phase assay development within the PHCS/CDx group. The role involves laboratory experimentation, scientific activities, manufacturing procedures, and basic computational data processing prior to clinical laboratory transfer.


Key Responsibilities:

  • Perform research, development, and manufacturing laboratory experiments.
  • Design, execute, interpret, and document experiments.
  • Prepare protocols, technical reports, summaries, and quantitative analyses.
  • Present experimental results to project and department teams.
  • Maintain accurate laboratory records and electronic documentation.
  • Follow GMP, GLP, Design Control, and applicable regulatory requirements.
  • Conduct assigned experiments independently and support team members with basic computational biology tasks, including running scripts and reading code.


Required Qualifications:

  • Bachelor’s degree in a relevant scientific field.
  • 0–2 years of relevant laboratory/industry experience.


Important: Candidates with a Master’s/PhD or >2 years of relevant experience are considered overqualified.


Interview: 15-minute video screen → On-site panel interview.



If interested, please send us your updated resume at

hr@dawarconsulting.com/akansha@dawarconsulting.com




Przegląd stanowiska

Typ stanowiska

Pełny etat

Wymagane umiejętności

Wet laboratory techniques (assay development)Experimental design and executionQuantitative data analysisTechnical writing (protocols and technical reports)Laboratory recordkeeping and electronic documentationGMP, GLP, and Design Control regulatory complianceLaboratory manufacturing proceduresPresenting experimental results and scientific communicationBasic computational biology and scripting (running scripts, reading code)Independent task management and execution of assigned experimentsTeam collaboration and supporting colleaguesLaboratory safety and standard operating procedure adherence

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