Innovative Assay Development Research Associate II/III

Dawar Consulting; Tucson (AZ); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical

Paid Sickleave

401K

Job summary

Dawar Consulting is seeking a Research Associate II & III for assay development in Tucson, AZ. The role involves designing, executing, and interpreting lab experiments to support Ventana projects, with rigorous documentation and GMP/GLP compliance.

Responsibilities include preparing technical reports, presenting results, troubleshooting, collaborating with teammates, and contributing to process improvements. A degree in life sciences and 2–6 years of related experience are preferred.

Qualifications

• Bachelor's degree in life sciences required.
• 2–6 years of relevant post‑college experience.
• Proficiency in wet laboratory techniques (e.g., pipetting, balance, stir plate).
• Capable of literature search and data interpretation; proficient with word processing, spreadsheets, and presentation software.
• Experience with SAFe/Agile planning processes (preferred).

Responsibilities

• Design and execute experimental protocols with minimal supervision; observe and analyze data.
• Prepare and present technical reports, summaries, and quantitative analyses; maintain accurate records.
• Troubleshoot problems and implement corrective actions.
• Collaborate in a team environment; contribute to project planning with creative input.
• Contribute to process improvement and assist in identifying patentable inventions.
• Train colleagues and ensure quality and adherence to the Quality First Time principle.
• Exercise judgment in selecting methods and techniques for complex problems.

Skills

Wet lab techniques

Pipetting

Literature search

Office software

Education

Bachelor's Degree in Life Sciences

Job description

Dawar Consulting is seeking a Research Associate II & III for assay development in Tucson, AZ. The role involves designing, executing, and interpreting lab experiments to support Ventana projects, with rigorous documentation and GMP/GLP compliance.

Responsibilities include preparing technical reports, presenting results, troubleshooting, collaborating with teammates, and contributing to process improvements. A degree in life sciences and 2–6 years of related experience are preferred.