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Integer Holdings Corporation

Medical device CDMO for cardiac devices

Quality Engineer 2

Quality EngineeringConfirmed live in the last 24 hours
Full-timeSpiddle West, An Spidéal, Co. Galway, IrelandNo salary listedIn-person

About the Job

Requirements

  • At a minimum, have earned a bachelor's degree in an engineering or related field and have 3 years of relevant experience; candidates who do not meet the education requirement may be considered with 7 or more years of relevant experience.
  • Have awareness of relevant domestic and international regulations and industry standards, such as ISO, QSR, UL, MDD, and TGA.
  • Have good knowledge of Microsoft Office.
  • Demonstrate the ability to work independently and collaboratively with associates and cross-functional teams.
  • Demonstrate technical aptitude and the ability to contribute effectively to a team or produce technical results individually.
  • Demonstrate written and oral communication competencies; candidates outside the United States must demonstrate written and oral English communication competencies.
  • Maintain a calm demeanor in a high-energy, constantly changing production environment.
  • Possess a positive, can-do attitude.

Responsibilities

  • Adhere to Integer’s values and all safety, environmental, security, and quality requirements, including Quality Management Systems, safety, environmental and security 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 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 assure Device History Records are complete and correct.
  • 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 materials.
  • Participate in continuous improvement projects and assist with product transfers.
  • Perform technical project work using standard quality management and production system methodologies to investigate opportunities for product and process improvements.
  • Collaborate with others, exchange information, ask questions, and regularly check for understanding to support development as an engineer.
  • 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; write, approve, and implement incoming, in-process, and final inspection procedures.
  • Ensure non-conforming material dispositions follow necessary procedures 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 analyses.
  • Apply standard data analysis practices and observe products and processes to establish root causes for product and process failures or support improvements to products and processes.
  • 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 and the quality improvement journey.
  • Perform other duties as needed and directed by line supervision.
  • Support manufacturing excellence and market-focused innovation strategies through site Hoshin Plans, Quality Plans, validation master plans, quality improvement initiatives, and regular updates to Quality Assurance and Regulatory Affairs weekly and monthly 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.
  • Actively support Environmental, Health and Safety programs and adhere to Integer values.
  • Work toward defined goals and objectives, including key projects and expected milestones.
  • Generate continuous improvement suggestions and support their implementation.

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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