Regulatory Documentation Coordinator - Thousand Oaks, CA

This role involves day-to-day administrative responsibilities onsite · and leading and supporting several project initiatives as needed. · ...

This role involves day-to-day administrative responsibilities onsite and leading and supporting several project initiatives as needed: · Manage the complete US FDA Certificate of Pharmaceutical Product (CPP) process — from application drafting and submission to Health Authorities ...

The Document Center Document Coordinator is responsible for the preparation and indexing of documents. · Process a daily, weekly and monthly quota of documents for scanning by researching, categorizing and organizing documents from departments through the organization. · ...

The Design Process Management Coordinator is responsible for maintaining the integrity and flow of technical documentation across engineering platforms. · 3-5 years of experience in document control, design registration, and project coordination · ...

Honda Racing Corporation seeks a Document Control Coordinator in Santa Clarita, CA. · ...

The Clinical Appeals Coordinator works in collaboration with the team of clinicians, coding professionals, physicians and HIM members to increase the team's program awareness, process and program benefits with the goal of decreasing denials, · enhancing performance and increasing ...

We are seeking a detail-oriented and proactive Deal Admin/Vehicle Documentation Coordinator to join our team. · In this vital role, you will manage the documentation process for vehicle transactions, ensuring accuracy, compliance, · and timely processing to adhere to California D ...

This role manages the end-to-end US FDA Certificate of Pharmaceutical Product (CPP) process and supports document authentication, dispatch, and archiving activities. · Manage the complete US FDA Certificate of Pharmaceutical Product (CPP) process from drafting through internation ...

This role involves day-to-day administrative responsibilities onsite leading and supporting several regulatory and documentation-focused projects. · ...

This role involves day-to-day administrative responsibilities onsite and leading and supporting several project initiatives as needed. · Manage the complete US FDA Certificate of Pharmaceutical Product (CPP) process — from application drafting and submission to Health Authorities ...

The role involves day-to-day administrative responsibilities onsite and leading and supporting several project initiatives as needed: Manage the complete US FDA Certificate of Pharmaceutical Product (CPP) process — from application drafting and submission to Health Authorities t ...

Manage the complete US FDA Certificate of Pharmaceutical Product (CPP) process — from application drafting and submission to Health Authorities through delivery to international destinations. · Serve as the primary liaison between FDA and internal requestors for issue resolution ...

The Multifamily and Commercial Superintendent is responsible for the on-site supervision and coordination of all construction activities for multifamily, · commercial or tenant improvement projects.This role ensures projects are delivered safely, on schedule, · written in accorda ...

The Multifamily or Commercial Project Manager is responsible for the overall planning, coordination, and execution of multifamily and Commercial construction projects from preconstruction through closeout. · This role oversees schedule, budget, contracts, and team performance to ...

We are seeking a detail-oriented Regulatory Operations Specialist to manage the end-to-end US FDA Certificate of Pharmaceutical Product (CPP) process and support document authentication regulatory coordination and project initiatives. · ...

In this vital role, you will join a team that interacts with Global Regulatory Affairs and Strategy (GRAAS) and CMC to communicate and advance processes in alignment with Amgen's company goals and objectives. · ...

The Senior Executive Administrator serves as a trusted partner to the Executive Director and a key member of the executive administrative team.This role requires exceptional organizational skill, discretion, emotional intelligence, and the ability to manage complex information, · ...

Support clinical distribution operations by managing order fulfillment coordinating logistics and ensuring timely accurate shipments of clinical materials Operate in a GMP regulated environment while following SOPs and maintaining compliance documentation Assist with inventory pr ...

This role involves interacting with Global Regulatory Affairs and Strategy (GRAAS) to advance processes in alignment with Amgen's company goals. · Manage the complete US FDA Certificate of Pharmaceutical Product (CPP) process. · Serve as the primary liaison between FDA and intern ...

+We're seeking a highly organized, proactive Executive Assistant to serve as a trusted partner to our CEO and Director of People Operations. · +Provide high-level administrative and operational support to the CEO. · Serve as the primary point of contact for the CEO. · ...