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Integer Holdings Corporation

Medical device CDMO for cardiac devices

NPI Quality Engineer 3

Quality EngineeringConfirmed live in the last 24 hours
Full-timeNew Ross, Co. Wexford, IrelandNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in an engineering or related field is required; candidates without the education requirement may be considered with 10 or more years of relevant experience.
  • At least 5 years of progressive engineering or technically focused experience is required.
  • Strong technical and problem-solving foundation, with training or certifications in problem-solving and project management methodologies such as Six Sigma; Green Belt is the minimum and Black Belt is preferred.
  • Awareness of relevant domestic and international regulations and industry standards, including ISO, QSR, UL, MDD, and TGA.
  • Good knowledge of Microsoft Office.
  • Solid technical aptitude and ability to contribute effectively to a team or produce technical results individually.
  • Written and oral communication competencies; outside the United States, written and oral English communication competencies are required.
  • Strong working knowledge of statistics and Minitab, at subject-matter-expert level.

Responsibilities

  • Apply engineering principles and practices to New Product Introduction projects and evaluate procedures to ensure production of quality products that meet or exceed internal and external customer expectations.
  • Develop approaches to complex problems, advance technology, and apply engineering concepts to resolve acute or chronic problems.
  • Conduct studies to understand process and measurement-system capability, and provide technical guidance to management as required.
  • Identify and develop documentation for process improvement and project implementation.
  • Maintain liaison with individuals and units inside or outside the organization, acting independently on technical matters in the field.
  • Adhere to safety, environmental, security, and quality requirements, including Quality Management Systems, U.S. Food and Drug Administration regulations, company policies, operating procedures, and other regulatory requirements.
  • Support regulatory and agency inspections, audits, investigations, and inquiries concerning control and assessment of product design and manufacturing quality.
  • Develop new test methods, including designing and manufacturing tooling, fixtures, and templates.
  • Test and validate new test methods, including gauge repeatability and reproducibility studies and statistical analysis using software such as Minitab.
  • Update test-method procedures and process standard operating procedures as required.
  • Provide technical input to root-cause analysis; generate investigation reports within key performance indicator metrics and timelines and route them for approval; participate in cross-functional New Product Introduction team reviews.
  • Review procedures, protocols, reports, and other documents related to test-method development, process testing, and process validation associated with New Product Introduction.
  • Lead a cross-functional project team, providing support and expertise for New Product Introduction, and provide technical input in accordance with the product development process and associated procedures.
  • Ensure compliance at all stages of the product development process.
  • Support planning and execution of risk-management activities according to ISO 14971.
  • Periodically review internal and external standards and identify potential gaps requiring action.
  • Lead continuous-improvement projects and assist with product transfers.
  • Work on technical projects using standard quality-management and production-system methodologies to investigate opportunities for product and process improvements.
  • Collaborate and exchange information with others, ask questions, and regularly check for understanding in support of development as an engineer.
  • Lead the generation and completion of protocols and reports for test-method validations.
  • Interface with Manufacturing Engineers to review new-product processes and coordinate process validations and capability studies; 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.
  • Ensure disposition of nonconforming materials follows procedures and corrective actions are adequate to prevent recurrence.
  • 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.
  • Apply standard data-analysis practices and observe products and processes to establish root causes of 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 investigation and implementation, and contribute to quality key performance indicators and the journey to 5 Sigma.
  • Align site Hoshin plans, quality plans, validation master plans, quality-improvement priorities, and regular quality assurance/regulatory affairs metrics updates with strategy.
  • Lead sustained change by ensuring customer change notifications are initiated and completed as necessary and supporting continuous-improvement activities.
  • Promote standardization through workplace organization and visual controls (5S), 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.
  • Optimize systems and processes through adoption of built-in-quality principles.
  • Actively support Environmental, Health and Safety programs and adhere to company values.
  • Work toward defined goals and objectives, key projects, and expected milestones; support continuous-improvement suggestions and their implementation.
  • Perform other duties as needed and directed by line supervision.

Desired Qualifications

  • A master's degree may be held.
  • Six Sigma Black Belt certification is preferred.

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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