Role: Senior Complaint Specialist – Investigation Lab. Location: San Diego, CA. Duration: 3 Months. Client: Medical. Role Summary. The Senior Complaint Specialist supports post-market surveillance for medical devices by investigating product complaints. This role focuses on analyzing failed products, identifying root causes, documenting findings, and ensuring complaints are handled accurately and in compliance with regulatory and quality requirem...
Quality Assurance & Compliance Specialist. Buchanan Ingersoll & Rooney is a national law firm with a proven reputation for providing progressive, industry-leading legal, business, regulatory and government relations advice to our regional, national and international clients. We are currently searching for an experienced. Quality Assurance & Compliance Specialist. for our. Pittsburgh. location to assist our Accounting team. This position utilizes ...
$45/hr - $47.29/hr. Title: QA Compliance Specialist (Data Review). Location: Westborough MA. Duration: 6 months. Description. The Compliance Specialist CMC, Quality Assurance will perform critical QA tasks in support of GMP and non-GMP manufacturing programs and Regulatory Submissions at Client. The successful candidate will foster data integrity, quality and compliance across a broad range of Quality Assurance areas and will work closely with ta...
Quality and Regulatory Compliance Specialist. Location: Richmond, VA- Onsite. Duration: 5 Months. Pay $40-$48/hr on w2. Shift: 1st Shift. 8AM TO 5PM. Role Purpose. Oversee and deploy risk-based Food Safety and Quality programs across internal/external manufacturing sites, suppliers, and licensed partners. Ensure full compliance with regulatory standards and client policies. Key Responsibilities. Support Business Units in applying and updating Glo...
Job Title. QA Compliance Specialist. Location. Columbus, OH. Contract type. W2. Shift. 8:30 AM – 5:00 PM. Job Summary. We are seeking a QA Compliance Specialist to support quality and regulatory compliance activities within a regulated medical device environment. This role is responsible for ensuring quality system processes comply with applicable regulatory requirements, international standards, and corporate policies. The ideal candidate will h...
Experience. Minimum of 6 years experience in biotech, pharmaceutical, or related industry or the equivalent combination of education/training and experience. Must have attention to detail and good investigation, problem solving, and organizational skills. This position requires a knowledge and experience with GxP processes related to managing vendors, partners, and suppliers. Familiarity with FDA Quality System Regulations and Pharmaceutical guid...
Job Description. The QA Compliance Specialist position exists to support the execution of quality & regulatory functions in the organization to ensure compliance of the AV-SH quality/business systems to applicable regulations, standards and corporate policies. Responsible for compliance with applicable Corporate and Divisional Policies and procedures. 1. Support external audit activities (FDA, FDB, ISO registrar audits etc.). 2. Audit areas of Ab...
Job Summary. The Quality Assurance Compliance Specialist supports the execution of quality and regulatory functions to ensure organizational compliance with applicable regulations, standards, and corporate policies. This role focuses on quality system administration, audit support, corrective action tracking, and cross-functional quality integration. Key Responsibilities. Support external audit activities, including FDA, FDB, ISO, and registrar a...
