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Quality Assurance Specialist

RbM Services, LLCKnoxville, Tennessee🇺🇸United StatesPosted Oct 13, 2026

Why This Role Stands Out

This hybrid Quality Assurance Specialist role at RbM Services offers a fantastic opportunity to contribute to cutting-edge medical device solutions within a supportive and collaborative team environment. You will thrive here if you possess a keen eye for detail and experience with quality management systems, with ample room for professional growth and skill development in a reputable company.

Quick Overview

Seniority
Mid Senior
Employment type
Full Time
Work mode
Hybrid
Location
Knoxville, Tennessee, United States
AuditingMicrosoft Office

Job Description

Quality Assurance Specialist
About Us
Founded in 2000 locally owned and operated, RbM Services is a growing turn-key design, manufacture, and service solution provider for medical devices in Tennessee's Technology Corridor. With over 100 years of combined experience in the medical device industry, our management staff has extensive experience in intellectual property development, contract design, product development, field service support, and product support of medical devices and laboratory instrumentation. Our team is passionate and even obsessed with providing solutions that deliver cutting-edge technology that improves patient experiences and outcomes. Our passion lies in the pursuit of perfection. We value our employee family and foster opportunities for us to engage in meaningful connections and we reward employees who exceed expectations.
Quality Assurance Specialist Job Description
The Quality & Regulatory Affairs Specialist will support the Q&RA Management team in ensuring compliance to regulations and standards and meeting customer requirements.
Responsibilities
  • Assist Q&RA Management with:
  • Development and revision of quality process documentation (SOPs, work instructions, forms & templates)
  • Documenting and following up on events (Nonconforming material, CAPA, audit findings, etc.)
  • Internal Auditing of the QMS
  • Quarterly Trending of Data
  • Training activities
Required Qualifications:
  • 2-5 years' experience in a Quality and Regulatory role (preferred Medical Device manufacturing)
  • Experience with ISO 9001 or 13485
  • Experience generating and revising QMS documentation
  • Microsoft Office Suite Proficient
  • Manage multiple assignments simultaneously
  • Excellent written and verbal communication skills

Benefits:
As a full-time team employee, you are eligible for all RbM Services benefits, including medical, dental, vision, long-term, short-term disability, 401k, PTO, 10 paid holidays, etc. All your information will be kept confidential according to the EEO guidelines

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