Associate Quality Engineer

Overview

A fast-growing diagnostics/medical device company in Springdale is expanding its Quality team. This is a strong entry-level opportunity to join a smaller organization where you can work across new product development
, manufacturing support, and quality system activities—gaining breadth and responsibility quickly.

We are hiring a Junior Quality Engineer to support day-to-day quality engineering activities across product development and manufacturing. You’ll work closely with Operations, R&D/Engineering, and Supply Chain and play a hands-on role in ensuring products meet regulatory and customer requirements.

• Support and maintain elements of the Quality Management System (QMS) (procedures, forms, records, document control)
• Assist with nonconformance investigations (NCRs), root cause analysis, and CAPA activities
• Support change control activities and ensure quality requirements are met during product/process changes
• Help with risk management documentation (e.g., basic DFMEA/PFMEA support, risk files, mitigation tracking)
• Support supplier quality activities (supplier documentation review, basic incoming inspection support, supplier issues)
• Assist with inspection/testing documentation
  , traceability records, and batch/device history record support where applicable
• Participate in internal audits and help with audit preparation (customer/regulatory) as needed
• Support continuous improvement initiatives focused on quality, yield, and compliance
• Help prepare and maintain quality metrics (KPIs) and contribute to problem-solving efforts

• Bachelor’s degree in Engineering, Quality, Chemistry, Biology, or related STEM discipline (or equivalent experience)
• 0–2 years of experience in a regulated manufacturing environment (medical device/IVD/biotech preferred)
• Basic understanding of quality fundamentals (documentation, investigations, corrective actions, compliance mindset)
• Strong attention to detail, ability to follow procedures, and comfort working hands-on in a fast-paced setting
• Strong communication skills and willingness to collaborate cross-functionally
• Ability to work onsite in Springdale, AR

• Exposure to ISO 13485 and/or 21 CFR 820 (training, coursework, internship, co-op, or work experience)
• Familiarity with CAPA
  , NCRs, root cause tools (5 Whys, Fishbone), and risk management basics
• Experience with document control systems, ERP/MRP, or basic data/Excel skills for reporting
• Internship/co-op experience in med device/diagnostics manufacturing

• Small team =
  high visibility and faster learning
• Hands-on exposure to new products and cross-functional work
• Growth pathway as the company scales (opportunity to take on more ownership quickly)