Research Associate I - Assay Development/Wet Laboratory

Dawar Consulting
  • Tucson, Arizona
  • Autofill and Review
30+ days ago

Job Description

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


 



Numbers & Facts

LocationTucson, Arizona
Websitewww.dawarconsulting.com

Skills

  • Assay Developmentunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Clinical Laboratoryunmatched
  • Data Processingunmatched
  • Documentationunmatched
  • GLP (Good Laboratory Practices)unmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Laboratoryunmatched
  • Manufacturingunmatched
  • Quantitative Analysisunmatched
  • Record Keepingunmatched
  • Regulatory Requirementsunmatched
  • Scripting (Scripting Languages)unmatched

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