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Integer Holdings Corporation

Medical device CDMO for cardiac devices

Quality Engineer 2-1

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 are required; 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, such as ISO, QSR, UL, MDD, and TGA.
  • Good 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 candidates 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 company values and all safety, environmental, security, quality, regulatory, policy, and operating-procedure requirements, including Quality Management Systems and U.S. Food and Drug Administration regulations.
  • Support regulatory and agency inspections, audits, investigations, and inquiries concerning 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 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.
  • Participate in continuous improvement projects and assist with product transfers.
  • Conduct technical projects using standard quality management and production system methodologies to investigate product and process improvement opportunities.
  • Generate and complete 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; write, approve, and implement incoming, in-process, and final inspection procedures.
  • Ensure non-conforming material dispositions meet applicable 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 analyses.
  • 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 investigations and implementation, and contribute to quality key performance indicators.
  • Support site Hoshin Plans, Quality Plans, validation master plans, quality improvement imperatives, and weekly and monthly Quality Assurance and Regulatory Affairs metrics.
  • Initiate and complete customer change notifications as necessary and support continuous improvement activities.
  • Support workplace organization and visual controls, Manufacturing Standard Work, and training and certification programs where applicable.
  • Promote standardized problem-solving methods, behavior-based safety programs, and improvement idea and suggestion systems.
  • Support optimization of systems and processes through built-in-quality principles.
  • Actively support Environmental, Health and Safety programs and adhere to company values.
  • Work toward defined goals, objectives, projects, and milestones; generate continuous improvement suggestions and support their implementation.
  • Perform other duties as needed and as 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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