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US_Research and Development Associate

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: Creative Solutions Services, LLC
Contract position
Listed on 2026-06-15
Job specializations:
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 28 - 32 USD Hourly USD 28.00 32.00 HOUR
Job Description & How to Apply Below
Position: US_Research and Development Associate I

and Development Associate I #26-01290

Up to $32 per hour NC Onsite

Job Title

Research and Development Associate I

Location

Research Triangle Park - Durham, NC

Pay Rate

$32/hr | Paid Weekly

Assignment Length

6-Month Contract (Potential Extension Based on Performance, Attendance & Business Need)

Benefits

Health, Dental & Vision Insurance Available

Position Overview

Seeking a Research and Development Associate I to support utility monitoring and quality control activities within a pharmaceutical manufacturing environment. This role is responsible for ensuring critical utilities and bulk gases meet quality and compliance standards through routine testing, sampling, inspection, and documentation.

Key Responsibilities
  • Perform TOC (Total Organic Carbon), Conductivity, and Nitrate testing for utility monitoring, cleaning verification, and validation activities.
  • Collect and analyze bulk gas samples for viable and non-viable particulates; may also perform moisture and THC testing.
  • Inspect process aids and raw materials, including filters and tubing.
  • Review and maintain GMP-compliant documentation.
  • Support environmental and utility monitoring programs.
  • Collaborate with Microbiology and Manufacturing teams to coordinate sampling activities and report monitoring data.
Qualifications
  • Bachelor's degree in Biology, Microbiology, Chemistry, Biochemistry, Environmental Science, or another scientific discipline.
  • 1–3 years of laboratory, quality control, environmental monitoring, utility monitoring, or GMP experience.
  • Experience with water testing (TOC, Conductivity, Nitrates), sample collection/testing, and GMP documentation preferred.
  • Strong attention to detail and ability to follow SOPs in a regulated environment.
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Position Requirements
10+ Years work experience
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