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Integer Holdings Corporation

Medical device CDMO for cardiac devices

Supervisor - Quality

Quality EngineeringConfirmed live in the last 24 hours
Full-timeHudson, MA, USAIn-person

About the Job

Requirements

  • A bachelor's degree in engineering or a related technical field is required.
  • At least 3 years of experience is required.
  • Knowledge and experience with the supported product line or function, such as manufacturing quality, supplier quality, or quality engineering, is required.
  • Specialized knowledge of relevant quality-system regulations and standards, such as EU MDR, ISO 13485, ISO 9001, Good Manufacturing Practices 21 CFR 820, and Good Documentation Practices, along with auditing experience, is required.
  • Ability to lead, create and share a coordinated vision, and align a team to resolve work is required.
  • Ability to work independently and collaboratively with associates and cross-functional teams is required.
  • Technical aptitude to contribute to a team or produce technical results individually is required.
  • Effective written, oral, and interpersonal communication skills, decision-making, and problem-solving skills are required.

Responsibilities

  • Coordinate team deliverables and provide daily direction to quality engineers and technicians to achieve quality requirements, performance goals, and improvement objectives for a manufacturing site.
  • Manage the performance, growth, and development of direct reports in support of the Quality Management System.
  • Follow company policies and procedures and applicable safety, quality, environmental, Food and Drug Administration, and other regulatory requirements.
  • Identify potential gaps in processes and systems and drive process improvements.
  • Supervise, coach, and direct quality professionals supporting product lines or process areas at a manufacturing site.
  • Provide first-level support for day-to-day issues raised by the team and seek cross-functional or organizational support when needed.
  • Review and approve engineering change requests, nonconformance reports, and engineering reports.
  • Establish daily, weekly, and monthly team objectives and maintain effective team communications; support direct reports in pursuing their Individual Development Plans.
  • Drive risk-based process control and ensure compliance with the established Quality Management System.
  • Build a culture of quality within the team and support adherence to the Quality Management System.
  • Support corrective and preventive action investigations and implementation, quality key performance indicators, and internal and external quality audits.
  • Apply data analysis and observe products and processes to determine root causes of product and process failures and justify improvements.
  • Ensure investigation and disposition of nonconforming materials follow 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 complaint, supplier quality, nonconforming material, training-effectiveness, and root-cause data and trends.
  • Support site strategy alignment through Site Hoshin Plans, quality-planning meetings, and regular updates to quality and regulatory affairs metrics.
  • Initiate and complete customer change notifications as needed and support continuous-improvement activities.
  • Promote standardization through workplace organization and visual controls, Manufacturing Standard Work, training and certification programs, and adoption of enterprise quality policies and procedures.
  • Promote associate engagement through standardized problem-solving methods, behavior-based safety programs, and improvement-idea systems.
  • Support manufacturing excellence through built-in quality, optimized scheduling and material-system designs, work-cell design, and total production maintenance.
  • Support Environmental, Health and Safety programs.
  • Achieve defined goals, objectives, project milestones, and scheduled tasks.
  • Generate continuous-improvement suggestions and support their implementation.
  • Promote associate engagement and ensure associate-relations issues are handled in a timely manner.
  • Perform other duties as needed and directed by the manager.

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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