I

Integer Holdings Corporation

Medical device CDMO for cardiac devices

Quality Engineer 3

Quality EngineeringConfirmed live in the last 24 hours
Full-timePembroke Pines, FL, USAIn-person

About the Job

Requirements

  • A bachelor's degree in an engineering or related field is required; candidates without this education may be considered with 10 or more years of relevant experience.
  • At least 5 years of progressive engineering or technically focused role experience is required.
  • A strong technical and problem-solving foundation is required; training and certifications in methodologies such as Six Sigma are preferred, with a green belt as the minimum and a black belt preferred.
  • Awareness of relevant domestic and international regulations and industry standards, including ISO, QSR, UL, MDD, and TGA, is required.
  • Good knowledge of Microsoft Office is required.
  • The candidate must be able to contribute effectively to a team or produce technical results independently.
  • Written and oral communication competencies are required; candidates outside the United States must demonstrate written and oral English communication competencies.
  • The candidate must maintain a calm demeanor in a high-energy, constantly changing production environment.

Responsibilities

  • Ensure internal and external customer expectations are met or exceeded by identifying and evaluating procedures that ensure quality product production.
  • Develop new approaches to complex problems and advance technology beyond previously achieved levels.
  • Apply engineering concepts to resolve acute or chronic problems.
  • Conduct studies to understand process and measurement-system capability and provide management with technical guidance as needed.
  • 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 role's field.
  • Comply with Integer 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, 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, ensure 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, control plans, and related documents for adequacy and correctness.
  • Lead continuous improvement projects and assist with product transfers.
  • Conduct technical project work using Integer's standard quality management and production system methodologies to investigate product and process improvement opportunities.
  • Collaborate with others 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 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, 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.
  • 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.
  • Apply standard data-analysis practices and examine products and processes to establish root causes of product and process failures or support improvement justifications.
  • 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 five sigma.
  • Perform other duties as needed and directed by line supervision.
  • Align work with site Hoshin plans, quality plans, validation master plans, quality-improvement imperatives, and regular updates to quality assurance and regulatory affairs weekly and monthly metrics supporting the five-sigma objective.
  • Ensure customer change notifications are initiated and completed as necessary, and support continuous improvement activities.
  • Promote workplace organization and visual controls (5S), Manufacturing Standard Work, and robust 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 Integer Environmental, Health and Safety programs and adhere to Integer values.
  • Work toward defined goals and objectives, key projects, and expected milestones.
  • Contribute continuous-improvement suggestions and support their implementation.

Desired Qualifications

  • A master's degree may be held.
  • Six Sigma training or certification is preferred, with a black belt 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

Recently Posted Jobs

Explore more opportunities at Integer Holdings Corporation

See more jobs