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 RegulationsAbility to manage multiple complex problems simultaneouslyAbility to be flexible in changing daily workload priorities as directedAbility to coordinate and synchronize multiple projectsAbility to conduct a significant amount of planning activities for self and othersAbility to take initiative and make decisions within company / departmental guidelinesAbility to thrive under challenging deadlines and in an energetic environmentAbility to work independently and in a team environmentExcellent attention to detail and organizationExcellent written and verbal communicationHighest level of ethics and integrityAbility to lead and motivate the right behaviorsStrong technical writingEffective project managementProficiency in Microsoft OfficeQualifications / Requirements
Bachelor's degree in a biological science, engineering, or related field requiredMaster's degree in a biological science, engineering, or related field preferredAt 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 engineeringASQ CQE certification preferredMust 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 essentialClearance of favorable background investigation required