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Integer Holdings Corporation

Medical device CDMO for cardiac devices

Quality Engineer 2

Quality EngineeringPosted on Nov 10
Full-timePlymouth, MN, USAIn-person

About the Job

Requirements

  • A Bachelor's degree in Engineering or a related field is required.
  • Two to five years of quality engineering experience is required, preferably in medical device or regulated manufacturing.
  • The ability to work independently and in a team environment is required.
  • The ability to communicate effectively in writing and verbally is required.
  • The ability to manage time effectively to ensure timely completion of tasks is required.
  • Competence in selecting and using Quality Engineering tools and techniques is required.
  • Good knowledge of interpreting and applying relevant domestic and international regulations and industry standards, such as ISO, QSR, UL, MDD, and TGA, is required.
  • Proficiency in Microsoft Office and Minitab is required.

Responsibilities

  • Provide Quality Engineering support for Operations to ensure Quality System requirements are followed for medical device manufacturing and operations in compliance with applicable regulatory and standards requirements.
  • Provide work direction for one to three technicians or inspectors.
  • Adhere to Integer Core Beliefs and all safety and quality requirements, including Quality Management Systems, Environmental Management Systems, U.S. Food and Drug Administration regulations, company policies and operating procedures, and other regulatory requirements.
  • Support regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
  • Monitor manufacturing of assigned products, assure compliance with Device Master Records, provide deviation and waiver guidance, and ensure complete and correct Device History Records are maintained.
  • Review the adequacy and correctness of changes to Bills of Materials, assembly procedures, drawings, component specifications, Failure Mode and Effects Analyses, control plans, and related documents.
  • Lead the generation and completion of protocols and reports for test method validations.
  • Interface with Manufacturing Engineers to review processes for new and existing products, coordinate process validations and capability studies, and recommend process monitoring devices where applicable.
  • Develop inspection techniques and procedures to ensure product integrity to design specifications, and write, approve, and implement incoming, in-process, and final inspection procedures.
  • Ensure the disposition of non-conforming materials meets regulatory requirements and that corrective actions are adequate to prevent recurrence.
  • Lead and manage complaint investigations.
  • Participate in plant Corrective and Preventive Action activities, including analysis of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root cause analysis.
  • Participate in continuous improvement projects.
  • Assist with product transfers.
  • Work with suppliers, management, engineers, and manufacturing associates to resolve quality problems, and assist these groups with capability studies and statistical quality control, including process capability index, design of experiments, and hypothesis testing.
  • Mentor and support quality inspectors and technicians.
  • Perform other functions as required.

About the Company

Integer Holdings Corporation

Medical device CDMO for cardiac devices

Integer Holdings Corporation is a large medical device CDMO that serves cardiac rhythm management, neuromodulation, and cardiovascular markets. It designs, develops, and manufactures device components and subassemblies through its brands Greatbatch Medical, Lake Region Medical, and Electrochem. The company differentiates itself by its scale, broad capabilities across multiple medical specialties, established brands, and global manufacturing footprint, enabling reliable supply for device makers. Its goal is to help medical device companies bring safe, effective technologies to market and improve patients’ lives worldwide.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Wilmington, DE
Founded
1940

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