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Director of Quality
Director of QualityExtremity Care • Conshohocken, PA, US
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Director of Quality

Director of Quality

Extremity Care • Conshohocken, PA, US
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Director Of Quality

The Director Of Quality is responsible for overseeing the quality management system and quality operations, to include document control, quality event investigations, customer feedback / complaints, design control, risk management, and quality control, while ensuring compliance with established standard operating procedures, FDA regulations, AATB Standards, ISO standards and other application regulations and industry standards.

Responsibilities

  • Define and promote a quality mindset throughout the organization
  • Develop, implement, and maintain procedures and controlled documents according to FDA regulations, AATB Standards, ISO Standards, and other applicable regulations
  • Provide subject matter expertise to drive improvements and decisions relating to the quality management system while supporting organizational strategic objectives
  • Oversee management of change control, the document change system, design control, record control, and periodic review of controlled documents and perform associated quality approvals
  • Lead training of new processes, process revisions, and corrective actions relating to quality
  • Oversee management and coordination of training requirements / assignments
  • Manage and oversee review of quality control records to include equipment cleaning, maintenance, environmental monitoring, supply inspections, and device / product inspections
  • Oversee management of deviations, nonconformances, complaints, CAPAs, SCARs, and safety incidents and ensure timely completion of associated investigations
  • Ensure adequacy of investigations with respect to root cause analysis and CAPA assessment
  • Conduct quality review and approval for closure of deviations, nonconformances, complaints, CAPAs, and SCARS
  • Lead risk management of department and ensure risks / issues are identified, addressed / reported, and where appropriate, escalated
  • Oversee, lead, and manage quality system related meetings including management review
  • Establish, evaluate, report, and provide improvements (where appropriate) for quality metrics
  • Provide quality oversight, support, and approval for new projects and products
  • Collaborate, review, and approve validation / verification / qualification plans, protocols, execution data, and summary assessments
  • Oversee and manage use of quality system software(s)
  • Support documentation requests from regulatory affairs department to support regulatory submissions (e.g. PMA supplements, 510(k) submissions)
  • Direct, participate, and / or support internal, client, and regulatory agency audits to ensure compliance with regulatory requirements, accreditation / certification requirements, and internal policies and standard operating procedures
  • Analyze data by conducting hypothesis, normal distribution, and process capability analysis testing
  • Develop and maintain professional working relationships with current and potential customers, consultants, suppliers, and vendors
  • Establish and execute continuing education strategy for department
  • Maintains company compliance and a working knowledge of FDA 21 CFR 1271, FDA 21 CFR 820, AATB standards, ISO Standards, cGMP / CGTP, other relevant regulations / standards, and internal organizational policies and standard operating procedures
  • Manage direct reports
  • Provide constructive feedback and guidance to develop leadership in direct reports and department management
  • Establish and monitor objective annual goals for direct reports
  • Conduct performance reviews and establish performance improvement plans as needed
  • Recruit, interview, and select personnel for hire
  • Travel domestically up to 25% to attend offsite meetings, conferences, and support business initiatives
  • Maintain acceptable attendance and punctuality for scheduled work hours and meetings
  • Ensure completion of assigned tasks and responsibilities within defined timeframes
  • Maintain flexibility to work outside of normal business hours during weekdays or weekends with reasonable advance notice to support business / operational needs when necessary
  • Perform other duties as assigned

Skills

  • Knowledge of FDA's Quality System Regulations, and the Canadian Medical Device Regulations
  • Ability to manage multiple complex problems simultaneously
  • Ability to be flexible in changing daily workload priorities as directed
  • Ability to coordinate and synchronize multiple projects
  • Ability to conduct a significant amount of planning activities for self and others
  • Ability to take initiative and make decisions within company / departmental guidelines
  • Ability to thrive under challenging deadlines and in an energetic environment
  • Ability to work independently and in a team environment
  • Excellent attention to detail and organization
  • Excellent written and verbal communication
  • Highest level of ethics and integrity
  • Ability to lead and motivate the right behaviors
  • Strong technical writing
  • Effective project management
  • Proficiency in Microsoft Office
  • Qualifications / Requirements

  • Bachelor's degree in a biological science, engineering, or related field required
  • Master's degree in a biological science, engineering, or related field preferred
  • At least 5-7 years of experience in an FDA regulated environment for medical device and / or pharmaceutical manufacturing, with at least 3-5 years in a management role for quality assurance, regulatory affairs, and / or engineering
  • ASQ CQE certification preferred
  • Must have DOE, Statistical Analysis, Quality System implementation, Quality Engineering Techniques, IQ / OQ / PQ, QSR (GMP) and ISO experience. Knowledge of basic statistical and engineering principles is essential
  • Clearance of favorable background investigation required
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    Director Of Quality • Conshohocken, PA, US

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