Senior Quality Engineer at NEXUSCW INC DBA NEXUS CONTINGENT W
RTP, NC 27709, USA -
Full Time


Start Date

Immediate

Expiry Date

19 Oct, 25

Salary

51.2

Posted On

20 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Excel, Statistical Data Analysis, Jmp, Completion

Industry

Information Technology/IT

Description

JOB POSTING: SENIOR QUALITY ENGINEER (BIOTECH) — RTP, DURHAM, NC

Location: RTP (Research Triangle Park), Durham, North Carolina (Onsite)
Start Date: July 21, 2025
Contract Duration: 12 months (anticipated length, with potential for extension)
Hourly Rate: $45-$51.20
Employment Type: W2 Contingent Workforce role through Nexus Contingent Workforce, contracted to a leading biotech company

✅ MEDICAL DEVICE AND/OR PHARMACEUTICAL INDUSTRY EXPERIENCE (REQUIRED)

✅ Strong background in risk management
✅ Hands-on experience with Batch Records / DHR
✅ Advanced skills in statistical data analysis (Excel, JMP, or similar)
✅ Solid experience with NCR / CAPA management
✅ Excellent technical writing skills (required)
✅ Familiarity with change control processes
✅ Ability to work independently and drive projects to completion

Responsibilities

ABOUT THE ROLE:

We are seeking an experienced Senior Quality Engineer to join the contingent workforce team supporting a leading biotech company in the RTP area. This is an exciting opportunity to contribute to a cutting-edge biotech company while working alongside some of the brightest minds in the industry.
As a Senior Quality Engineer, you will play a critical role in ensuring the highest standards of quality and compliance, driving continuous improvement, and supporting key quality systems and processes. This is a W2 contingent role contracted through Nexus Contingent Workforce with an anticipated assignment length of 12 months and the potential for ongoing extension.

KEY RESPONSIBILITIES:

  • Lead and execute risk management activities in accordance with regulatory requirements
  • Review and manage Batch Records and Device History Records (DHR) for accuracy and compliance
  • Perform statistical data analysis using Excel, JMP, or equivalent tools to support quality improvement initiatives
  • Lead and manage NCR (Nonconformance Reports) and CAPA (Corrective and Preventive Actions) processes
  • Draft clear, precise, and compliant technical documents, reports, and protocols
  • Oversee change control activities to ensure smooth and compliant implementation
  • Work independently with minimal supervision, while collaborating effectively across cross-functional teams
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