Regulatory Affairs Specialist Jobs in Pomona, CA

The Specialist in Regulatory Affairs will represent the regulatory function on manufacturing and product development teams, ensuring compliance with regulatory requirements. This role involves prepari...

The Senior Specialist in Regulatory Affairs will guide innovative cardiac surgery technologies through complex international regulatory environments, ensuring compliance and facilitating product appro...

The Sr. Specialist, Regulatory Affairs is responsible for developing and executing regulatory strategies for Neurovascular and Peripheral devices to ensure compliance with FDA and international regula...

The Manager, Regulatory Affairs - CMC at AstraZeneca is responsible for developing and executing the CMC regulatory strategy for innovative T cell therapies. This role involves collaborating with cros...

The Principal Regulatory Affairs Specialist is responsible for developing and authoring regulatory submissions for medical devices, ensuring compliance with global regulations. This role involves prov...

The Senior Regulatory Specialist will support permitting needs by preparing permit applications for various regulatory agencies, including the U.S. Army Corps of Engineers and California Coastal Commi...

The Clinical Trials Regulatory II Specialist will support the Blood and Marrow Transplantation & Cellular Therapy program by preparing regulatory submissions and managing compliance with IRB, FDA, and...

The Associate Director of Regulatory Affairs - CMC is responsible for developing and executing the CMC regulatory strategy for early-stage T cell therapies. This role involves managing regulatory doss...

The Senior Regulatory Affairs Specialist in Cardiac Rhythm Management at Abbott leads the preparation and submission for regulatory approvals, providing guidance to cross-functional partners. This rol...

The Pharmacovigilance Specialist provides operational support for global pharmacovigilance activities related to the company's marketed products. This role involves managing adverse events, ensuring c...

The Manager of Regulatory Affairs is responsible for developing and implementing a compliance program to ensure adherence to applicable laws and regulations within Jefferson's various business units...

The Senior Specialist in Quality Assurance is responsible for ensuring that products and services comply with regulatory standards and specifications. This role involves handling CGMP documentation, p...

The Director of Quality Control and Regulatory Affairs is responsible for ensuring compliance with quality systems, cGMP, and cGTP models, as well as all applicable regulations. This role involves mon...

The Director of Global Regulatory Affairs - Corporate will lead the development and implementation of regulatory strategy for multiple complex projects, manage a team, and collaborate with regional le...

The Director of Regulatory Affairs leads efforts to ensure compliance with regulatory standards and oversees communication with accrediting and licensing agencies in healthcare settings...

The Sr. Quality Specialist will lead continuous improvement initiatives to enhance product/service quality, operational efficiency, and customer satisfaction. The role involves creating and enforcing...

The Senior Quality Compliance Specialist will be responsible for planning, performing, and documenting QMS compliance audits, managing Audit CAPA corrective actions, and supporting internal and extern...

The Senior EHS Specialist at Abbott in Irvine, CA will work under general supervision to organize and plan EHS program support activities, ensure compliance with environmental, health, and safety regu...

The Senior Manager, Global Regulatory Strategy at AbbVie is responsible for representing regulatory affairs in device development and marketed product projects. The role involves developing, communica...

Evolus is seeking an experienced Sr. Regulatory Affairs Manager to develop US and global regulatory strategies for Drugs and Biologic products. The role involves leading regulatory submissions, provid...

The Clinical Affairs Specialist at FUJIFILM Irvine Scientific will assist in developing Clinical Evaluation Plans and Reports, conduct clinical literature searches, and evaluate clinical data for medi...

The Pharma R&D Regulatory Affairs Manager will lead and deliver engagements focused on implementing innovative business and technology solutions within the pharmaceutical regulatory affairs sector. Th...

The Pharma R&D Regulatory Affairs Manager will lead and deliver engagements focused on implementing innovative business and technology solutions within the pharmaceutical regulatory affairs sector. Th...

The Manager, Regulatory Counsel will provide legal guidance to Edwards, focusing on the review and analysis of advertising and promotional materials to ensure compliance with regulations. This role in...

Evolus is seeking an experienced Regulatory Affairs Manager to join their team, focusing on regulatory submissions and compliance for drug and biologic products globally. The role involves managing re...