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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-timeSanto Domingo, Dominican RepublicNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in an engineering or related field and 3 years of relevant experience; candidates who do not meet the education requirement may be considered with 7 or more years of relevant experience.
  • Awareness of relevant domestic and international regulations and industry standards, including ISO, QSR, UL, MDD, and TGA.
  • Knowledge of Microsoft Office.
  • Ability to work independently and collaboratively with associates and cross-functional teams.
  • Technical aptitude to contribute effectively to a team or produce technical results individually.
  • Written and oral communication competencies.
  • For roles outside the United States, written and oral English communication competencies.
  • Ability to maintain a calm demeanor in a high-energy, constantly changing production environment.

Responsibilities

  • Adhere to Integer's Values and all safety, environmental, security, and quality requirements, including Quality Management Systems, FDA regulations, company policies and operating procedures, and other regulatory requirements.
  • Support regulatory and agency inspections, audits, investigations, and inquiries related to 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.
  • Perform technical projects using standard quality management and production system methodologies to investigate product and process improvement opportunities.
  • Collaborate with others, exchange information, ask questions, and check for understanding in support of professional development.
  • 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 disposition of non-conforming materials follows required 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 analysis.
  • Apply standard data-analysis practices and observe products and processes to establish root causes for 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 investigations and implementation, and contribute to quality key performance indicators and quality improvement.
  • Support site Hoshin plans, quality plans, validation master plans, associated quality-improvement initiatives, and regular updates to quality assurance and regulatory affairs weekly and monthly metrics, supporting progress toward five sigma.
  • Ensure customer change notifications are initiated and completed as necessary, and support 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 methodologies, behavior-based safety programs, and improvement idea and suggestion systems.
  • Support systems and process optimization through adoption of built-in-quality principles.
  • Support Integer Environmental, Health and Safety programs.
  • Work toward defined goals and objectives specifying key projects and expected milestones.
  • Generate continuous improvement suggestions and support their implementation.
  • Perform other duties as needed and directed by line 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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