Quality Control Specialist

1 month ago


Logan, United States Systematic Business Consulting Full time

Join a high-growth manufacturing company active in multiple market areas as a Quality Systems Specialist in Logan, UT. This role supports the creation, development, management, maintenance, control, and improvement of the Quality Management System and its corresponding processes, procedures, work instructions, and records.

This opportunity allows for every other Friday off

Responsibilities:

  • Quality Planning
  • Quality Management System Support
  • Corrective and Preventive Action (CAPA)
  • Nonconforming Product
  • Quality Complaint Handling
  • Internal Audits / External Audits
  • Quality Training
  • Process Control and Quality Improvement.
  • Document Control and Record Control

Requirements:

  • Bachelor's degree (B.S.) degree in Life Science or Engineering discipline. -Preferred
  • 3 years of Quality or R&D related experience with medical devices, in the manufacturing industry; w/ degree, Or 5 years of direct Quality or Regulatory related experience w/o a degree -Required
  • Knowledge and skills in the use of advanced computer programs (spreadsheets, database manipulation, cloud-based software, and flow)- Required
  • Knowledge of ISO13485 quality system and/or FDA 21 CFR 820 quality - Required
  • Practical experience/training in quality planning, Corrective/preventive actions systems, quality auditing, root cause analysis, and problem-solving are highly desirable. - Preferred
  • Experience in implementing eQMS software, or years of experience using eQMS software. Preferred.
  • Describe Medical Devices Single Audit Program (MDSAP) experience in compliance of a quality management system (QMS). Preferred

by Jobble



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