Quality Engineer

IntePros

$70K — $95K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Biomedical or Mechanical Engineering or related field
  • 1+ years of industry experience
  • Knowledge of Change Management and Quality Management Systems (QMS)
  • Strong problem-solving and critical thinking skills
  • Ability to independently apply engineering rationale
  • Experience with validation processes
  • Excellent communication skills and attention to detail
  • Proficiency in Microsoft Word, Excel, and PowerPoint

Responsibilities

  • Provide quality engineering support across quality assurance and preventative activities
  • Develop and implement methods and procedures for process control and improvement
  • Support validation projects for new equipment and processes
  • Execute First Article Inspection (FAI) strategy development and approvals
  • Create and update Standard Operating Procedures (SOPs) through change management
  • Collaborate with teams to implement risk-based process controls
  • Apply independent judgment and professional expertise in quality processes

Benefits

  • Opportunity for career growth and development
  • Collaborative work environment with cross-functional teams
  • Chance to influence manufacturing processes and quality standards
  • Exposure to validation and quality assurance in the medical device field
  • Potential for flexible work arrangements within a structured environment
Full Job Description
Quality Assurance Engineer
Mahwah, NJ (minimum 3 days on-site)

Role Overview:
As a Quality Engineer, you will provide quality engineering support across quality assurance, control, and preventative activities within operations and other business functions. You'll develop and implement methods and procedures for process control, process improvement, testing, and inspection to ensure products meet design and quality standards.
You will support:
  • Validation projects for new equipment and processes introduced to the plant
  • First Article Inspection (FAI) strategy development, execution, and approvals
  • Standard Operating Procedure (SOP) and inspection plan creation/updates through change management
You'll collaborate with Manufacturing Engineering, Sterility Assurance, and Design teams to implement risk-based process controls and equipment maintenance measures for new equipment.
This is an individual contributor role requiring independent judgment and professional expertise, typically suited to someone with a university degree or equivalent practical experience.

Required Qualifications:
  • Bachelor's degree in Biomedical Engineering, Mechanical Engineering, or related field
  • 1+ years of industry experience
  • Knowledge of Change Management and Quality Management Systems (QMS)
  • Strong problem-solving and critical thinking skills
  • Ability to independently apply engineering rationale to decisions
  • Experience with validation processes
  • Excellent communication skills (oral and written) and attention to detail
  • Proficiency in Microsoft Word, Excel, and PowerPoint
Preferred Qualifications:
  • Understanding of medical device concepts, ISO 13485, GDP, and GMP
  • Experience developing or approving SOPs
  • Familiarity with risk-based and statistical concepts
  • Self-starter, comfortable in a fast-paced, multi-site team environment
Travel: Not typically required; occasional travel possible (up to 10%)

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