Quality Engineer I- Alden Ny

Integer

Alden, New York, United States
Min 59,250; max 86,900; benefits: medical, dental,...
Not specified (likely onsite based on the nature of the role)
Quality management systems (qms)
Fda regulations
Device history records (dhr)
Integer is seeking a Quality Engineer I for their Alden, NY location, aimed at ensuring compliance with quality standards in the manufacturing of medical devices. The role is entry-level, focusing on engineering methods, quality assurance, and collaboration with experienced engineers to meet customer expectations

Job Summary

  • As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization.
  • You will support regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
  • Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer’s success.

Matching Summary

Match Score: 75

Integer is seeking a Quality Engineer I for their Alden, NY location, aimed at ensuring compliance with quality standards in the manufacturing of medical devices. The role is entry-level, focusing on engineering methods, quality assurance, and collaboration with experienced engineers to meet customer expectations.

Salary

Min 59,250; Max 86,900; Benefits: medical, dental, vision, disability, life insurance, adoption benefits, parental leave, 401(k) with company matching, 80 hours holidays, paid time off

Skills & Requirements

Must-have

  • Quality Management Systems (QMS)
  • FDA regulations
  • Device History Records (DHR)
  • Bill of Materials (BOM) review
  • Continuous improvement projects
  • Product and process improvements
  • Test method validation protocols
  • Process validation and capability studies
  • Inspection techniques and procedures
  • Non-conforming material disposition
  • Corrective and preventive actions (CAPA)
  • Data analysis practices
  • Internal quality audit activities
  • Manufacturing Excellence strategies
  • Market Focused Innovation strategies
  • Hoshin Plans
  • Validation master plans
  • Workplace organization & visual controls (5S)
  • Manufacturing Standard Work
  • Standardized problem solving methodologies
  • Behavior-based safety programs
  • Built-in-quality principles

Nice-to-have

  • Collaborate with others
  • Exchange of information
  • Ask questions and check for understanding
  • Calm demeanor in high energy environment
  • Positive, can-do attitude
  • Belief that failure is not an option

Key Requirements

  • Bachelor's degree in engineering or related technical/Science field
  • 0-3 years of experience
  • Awareness of Domestic and International Regulations and Industry Standards
  • Good knowledge in Microsoft Office
  • Ability to work independently and collaboratively
  • Solid technical aptitude
  • Competencies in written and oral communications

Work Rights

Not specified

Tailored Resume

Cover Letter