Associate Director Quality Assurance

Associate Director Quality AssuranceLocation: Raleigh, NCPay Rate: $45-50/HR Monday to Friday, from 8:00 to 5:00, 3 days a week in the Raleigh officeThe Associate Director, Quality Assurance, is responsible for the global strategic management and oversight of R&D Quality activities and associated staff related to Good Manufacturing Practices (GMP) for non-Energy Based Devices (EBD) and EBD Medical Devices. Activities include, but not limited to general Product Development / Design Control customer input, specification development, verification and validation testing, manufacturing transfer, risk assessment, usability, design change control, etc. This role will operate as a liaison among the various R&D functions and the Quality Operations department to assure global strategic alignment and compliance.Major DutiesStaff Management: Responsible for the management of global R&D Quality staff including performance management, training, coaching, mentoring, and task oversightR&D Quality Management and Oversight: Responsible for the global strategic oversight of R&D Quality GMP activities as related to Medical Devices (non-EBD and EBD) in support of Project Teams and R&D overall to assure global compliance. Including:Quality activities for medical device manufacturing and Design & Development activities throughout all stages of the device development process (e.g. general Product Development / Design Control customer input, specification development, verification and validation testing, manufacturing transfer, risk assessment, usability, design change control).Leading teams through Design Control requirements while maintaining compliant Design History Files and support tech transfers to manufacturing.R&D quality oversight of preclinical and clinical planning and readiness activities.R&D quality oversight of document reviews and regulatory submissions in support of business objectives.Oversee R&D Quality project timelines as defined by department, project team, and business objectives.Quality activities for medical device manufacturing and Design & Risk Management: Oversee risk management activities throughout all stages of the device development process.Human Factors Engineering: Oversee human factors/usability activities throughout all stages of the device development process.Audits: Oversee audits (e.g., internal, vendor/supplier), as needed. Vendors/suppliers qualifications. All Merz regulatory authority inspections and certification body audits, as applicable.General R&D Support: Support R&D related activities including but not limited to SOP creation and maintenance, NCRs, DCNs, CAPAs, deviations, change requests, archival, corporate, and departmental initiatives.R&D Quality Improvements: Facilitate and support harmonization initiatives within the R&D group. Facilitate and support projects to improve R&D compliance and operational efficiencies.Quality Intelligence: Stay informed of the latest updates related to applicable regulations to ensure R&D Quality policies and procedures remain compliant as related to Medical Devices. Provide updates to R&D staff, as applicable.Further Tasks: Communicate effectively cross-functionally and raise questions/issues to the attention of executive management, as appropriate. Provide support to other R&D staff as needed and perform duties and assignments as required.Other duties as assigned: Additional duties as needed to support the business and overall company objectives.Leadership ResponsibilitiesArticulate a clear and compelling vision aligned with the global cultural tenets and strategic objectives of the company. Clearly define roles and responsibilities while holding members accountable for their performance. Develop talent and skills of individual team members Empower leaders and employees to make informed decisions, enabling autonomy while providing guidance and support.EducationBachelor's Degree in Engineering or Life/Health Sciences Preferred: Master's DegreeAdditional Licenses and CertificationsCertification(s) – ASQ Certified Quality Engineer or equivalent - preferredTechnical & Functional SkillsProficient in all MS Office applications Demonstrated organizational skills, ability to independently prioritize work and detail oriented Strong verbal, written communication, and emotional intelligence skills Ability to effectively multitask and manage multiple projects Experience with FDA, European agency regulations, cGMP regulations, and Quality Management software is highly preferred. Knowledge of regulatory requirements and standards for a medical device organization (i.e., 21CFR820, ISO 13485, ISO 14971, IEC 62304) Ability to work effectively in a global, matrix environment Ability to travel up to 15%Physical RequirementsThis job requires various physical activities and environmental conditions that employees must be prepared to handle. Key physical requirements include standing, sitting, walking, and bending, with tasks involving repetitive movements and handling objects of different weights, ranging from light (under 5 lbs) to heavy (over 20 lbs). Employees will also need to operate machinery such as computers, copiers, and telephones, and perform tasks requiring manual dexterity and visual acuity. The working environment may expose employees to different temperatures, noise levels, and other conditions like humidity and heights. Sensory requirements include near and far visual acuity, color discrimination, hearing, and speech. Additionally, some roles may involve local, national, or international travel (up to 20%). These requirements ensure that the job is performed effectively while accommodating employees' needs in compliance with the Americans with Disabilities Act (ADA).Work Experience7 - 8 years of relevant Quality medical device development experience Energy-Based Device Experience Knowledge of Class II, 510K, 21CFR 820, ISO 13485, IEC 606011, ISO 14971