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Integer Holdings Corporation

Medical device CDMO for cardiac devices

Quality Engineer 2-2

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, 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.
  • Solid technical aptitude and ability to contribute 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.

Responsibilities

  • Follow Integer's 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 for compliance with Device Master Records, provide deviation and waiver guidance, and ensure complete and correct Device History Records are maintained.
  • Review the adequacy and correctness of changes to Bills of Materials, assembly procedures, drawings, component specifications, Failure Modes and Effects Analyses, control plans, and related materials.
  • Participate in continuous improvement projects and assist with product transfers.
  • Investigate opportunities for product and process improvements using Integer's standard quality management and production system methodologies.
  • Collaborate with others, exchange information, ask questions, and check for understanding to support development as an engineer.
  • Lead 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 to design specifications, and write, approve, and implement incoming, in-process, and final inspection procedures.
  • Ensure dispositions of non-conforming materials follow necessary 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, non-conforming 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 product and process 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 and quality improvement goals.
  • Perform other duties as needed and directed by the line of supervision.
  • Support manufacturing excellence and market-focused innovation strategies through site Hoshin plans, quality plans, validation master plans, quality improvement initiatives, and regular updates to quality assurance and regulatory affairs weekly and monthly metrics supporting the walk to five sigma.
  • Initiate and complete customer change notifications as necessary and support sustained change and 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.
  • Actively support Environmental, Health and Safety programs and adhere to Integer's Values.
  • Work toward defined goals and objectives, including key projects and expected milestones.
  • Generate continuous improvement suggestions and support their implementation.

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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