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Integer Holdings Corporation

Medical device CDMO for cardiac devices

Quality Engineer 1

Quality EngineeringConfirmed live in the last 24 hours
Full-timeHudson, MA, USAIn-person

About the Job

Requirements

  • Perform work using general engineering methods and tools with direction, instruction, and guidance from more experienced engineers and managers.
  • Adhere to company values and applicable safety, environmental, security, quality, regulatory, policy, and operating-procedure requirements, including Quality Management Systems and U.S. Food and Drug Administration regulations.
  • Collaborate with others, exchange information, ask questions, and regularly check for understanding.
  • Use standard quality management and production system methodologies and standard data analysis practices.
  • Ensure non-conforming material dispositions follow required procedures and corrective actions are adequate to prevent recurrence.

Responsibilities

  • Support quality activities at a high-volume hydrophobic coating plant, including material review board support, corrective and preventive action management, complaint investigation, audit support, change management, new product introduction activities, and continuous improvement.
  • Support regulatory and agency inspections, audits, investigations, and inquiries regarding control and assessment of product design and manufacturing quality.
  • Monitor manufacturing of assigned products for compliance with device master records, provide deviation and waiver guidance, and ensure complete and correct Device History Records are maintained.
  • Review changes to bills of materials, assembly procedures, drawings, component specifications, failure mode and effects analyses, and control plans for adequacy and correctness.
  • Participate in continuous improvement projects and assist with product transfers.
  • Work on technical projects to investigate opportunities for product and process improvements.
  • Support 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 against design specifications; write, approve, and implement incoming, in-process, and final inspection procedures.
  • 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 analyses.
  • Observe products and processes to establish root causes for product and process failures or justify improvements.
  • Support internal quality audit activities as applicable.
  • Assure adherence to the Quality Management System, support corrective and preventive action investigations and implementation, and contribute to quality key performance indicators.
  • Support strategy alignment through site Hoshin Plans, Quality Plans, validation master plans, quality improvement imperatives, and updates to quality assurance and regulatory affairs metrics.
  • Ensure customer change notifications are initiated and completed as necessary, and support continuous improvement activities.
  • Support standardization through workplace organization and visual controls, manufacturing standard work, and training and certification programs where applicable.
  • Promote associate engagement through standardized problem-solving methodologies, behavior-based safety programs, and improvement idea and suggestion systems.
  • Support systems and process optimization through adoption of built-in-quality principles.
  • Perform other duties as needed and directed by the line of supervision.

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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