Quality Director Jobs in Usa
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Director, Clinical Quality
Title: Director, Clinical QualityLocation: Hybrid/Flexible in Boston (Must be in MA) Position OverviewThe Director of Clinical Quality is responsible for leading Clinical Quality Assurance (CQA) activities for assigned clinical development programs. This role oversees audits, manages quality issues, conducts investigations, and ensures inspection r...
Director, Clinical Quality
Title: Director, Clinical QualityLocation: Hybrid/Flexible in Boston (Must be located in MA) Position OverviewThe Director of Clinical Quality is responsible for leading Clinical Quality Assurance (CQA) activities for assigned clinical development programs. This role oversees audits, manages quality issues, conducts investigations, and ensures insp...
Director of Quality
Director of Quality - Sterile ManufacturingAlbany, OH | Full-Time | On-SiteWe're working with a growing pharmaceutical manufacturer focused on sterile injectables to find an experienced Director of Quality to lead Quality Assurance and Quality Control operations at their 503B facility in Ohio. This is a key leadership role where you'll drive qualit...
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Director, Quality Compliance
The Director of QA Compliance, you will lead and manage all aspects of Quality Compliance. This includes overseeing Quality Systems (incident resolution, CAPAs, change control, complaint resolution), hosting FDA inspections, and responding to inspection queries. You will also oversee site-wide compliance improvements, conduct internal and external ...
Director, GMP Quality
Title: Director, Quality (GMP)Location: Cambridge, MA (Hybrid) Position SummaryThe Director of Quality & Compliance (GMP) plays a vital leadership role within the Quality & Compliance function, providing operational, regulatory, and system-level expertise for GMP-related activities. This individual will ensure that all GMP efforts-whether executed ...
Sr. Clinical QA Specialist
Position Summary:The Clinical Quality Assurance (QA) Specialist is responsible for ensuring the quality and compliance of clinical studies and activities in accordance with applicable regulatory requirements, including FDA 21 CFR Part 812, ICH GCP, ISO 14155, and company SOPs. This role supports the development, execution, and continuous improvemen...