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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-timeBrooklyn Park, MN, USAIn-person

About the Job

Requirements

  • A bachelor's degree in an engineering or related field; a master's degree may also be held.
  • At least 5 years of progressive engineering and/or technically focused role experience; candidates who do not meet the education requirement may be considered with 10+ years of relevant experience.
  • Strong technical and problem-solving foundation, with preferably training and certifications in problem-solving and project-management methodologies such as Six Sigma; Green Belt is a minimum and Black Belt is preferred.
  • Awareness of relevant domestic and international regulations and industry standards, such as ISO, QSR, UL, MDD, and TGA.
  • Good knowledge of Microsoft Office.
  • Strong working knowledge of statistics and use of Minitab, with subject-matter expertise in statistics.
  • Competence in written and oral communication; candidates working outside the United States must also demonstrate written and oral English communication competence.

Responsibilities

  • Apply engineering principles and practices to New Product Introduction (NPI) projects, evaluate procedures, and 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 of 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 on technical matters.
  • Comply with the Quality Management System (QMS), safety, environmental, security, FDA, company-policy, operating-procedure, and other regulatory requirements.
  • Support regulatory and agency inspections, audits, investigations, and inquiries concerning product design and manufacturing quality.
  • Develop new test methods, including designing and manufacturing tooling, fixtures, and templates; validate test methods, conduct gage repeatability and reproducibility (R&R) studies, and analyze data statistically 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 timelines and route them for approval; participate in cross-functional NPI team reviews.
  • Review procedures, protocols, reports, and other documents related to test-method development, process testing, and process validation for new product introduction.
  • Lead cross-functional project teams and provide NPI support and expertise; participate in the product development process and ensure compliance at all stages.
  • Support planning and execution of risk-management activities under ISO 14971; review internal and external standards periodically and identify potential gaps requiring action.
  • Lead continuous-improvement projects, assist with product transfers, and investigate opportunities for product and process improvement using standard quality-management and production-system methodologies.
  • Lead generation and completion of protocols and reports for test-method validations.
  • Work 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, and write, approve, and implement incoming, in-process, and final inspection procedures.
  • Ensure non-conforming material dispositions follow required procedures and corrective actions are adequate to prevent recurrence.
  • Participate in plant corrective and preventive action (CAPA) activities, analyzing 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 support improvement justifications.
  • Support internal quality audits as applicable; uphold the QMS, support corrective and preventive action investigations and implementation, and contribute to quality key performance indicators and the site's 5 Sigma goal.
  • Support site strategy through site Hoshin plans, quality plans, validation master plans, quality-improvement initiatives, and regular updates to quality assurance/regulatory affairs metrics.
  • Lead sustained change by ensuring customer change notifications are initiated and completed and supporting continuous-improvement activities.
  • Support 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 methods, behavior-based safety programs, and improvement-idea and suggestion systems.
  • Support systems and process optimization through built-in-quality principles.
  • Actively support environmental, health, and safety programs; meet defined goals, objectives, project milestones, and quality measures; generate and support implementation of continuous-improvement suggestions.
  • Perform other duties as needed and directed by line supervision.

Desired Qualifications

  • Training and certifications in problem-solving and project-management methodologies, including Six Sigma Green Belt; Black Belt 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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