Document Control Specialist – Pharma/Biologics - Seattle

The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Jump site, · including the document change control process, issuance and reconciliation of batch records, batch related forms, · and management of archi ...

The primary responsibility of the Training Specialist is to conduct training needs analysis for departmental and business system training programs. · ...

The primary focus of the Quality Control Associate I role will be to support drug product lot release and in-process testing within a cGMP environment.Perform or support cGMP lot release, · in-process,and stability testing using various software packages. · ...

The primary focus of the Manufacturing Associate I role will be cellular therapeutic manufacturing at JuMP during process transfers, · routine production,and technology improvements. · ...

The primary focus of the Quality Control Associate I role will be to support drug product lot release and in-process testing within a cGMP environment. · ...

This role plays a key role in supporting cGMP quality operations for the Bothell Manufacturing Plant (Jump) and is an individual contributor responsible for leading/facilitating triages, deviation approvals, and CAPA records through the electronic quality record management system ...

Job summary · A Project Management Specialist II provides critical support to the R&D Portfolio Management team across pharmaceutical and medical device programs.The position focuses on managing timelines, project documentation and operational activities to ensure smooth executio ...

+Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. · +Work closely with leadership and program managers to set clear project schedules/planning, budgets and deliverables. · Monit ...

The Project Management Specialist II provides critical support to the R&D Portfolio Management team across pharmaceutical and medical device programs. · Work closely with leadership and program managers to set clear project schedules/planning budgets and deliverables. · ...

We are seeking a Computer System Validation Engineer – Pharma for a global pharmaceutical client. · ...

Seeking an experienced Automation Specialist to develop program and qualify automated QC methods for cell therapy assays in GMP environment. · ...

We are seeking a Computer System Validation Engineer for a global pharmaceutical client. · ...

We are the largest nonprofit fighting poverty, disease, and inequity around the world. · The Foundation · We provide an exceptional benefits package to employees and their families which include comprehensive medical, dental, · and vision coverage with no premiums, · generous pai ...

The Foundation We are the largest nonprofit fighting poverty disease and inequity around the world. · We believe our employees should reflect the rich diversity of the global populations we aim to serve. · We provide an exceptional benefits package to employees and their families ...

As Sr. Program Officier, you contribute to a productive and collaborative culture of innovation to accelerate translation of research into practical health solutions. · The Foundation provides an exceptional benefits package including comprehensive medical, dental and vision cove ...

+The Senior Program Officer, Vaccine Discovery role is a critical position focused on driving innovation and impact in global vaccine discovery and development. · +Support and execute the Vaccines Discovery strategy in a creative, rigorous, innovative, data-driven, analytical man ...

The Foundation is the largest nonprofit fighting poverty, disease and inequity around the world. This role is critical to driving innovation and impact in global vaccine discovery and development.We are seeking a highly experienced professional with deep expertise in human immuno ...

We are seeking an Automation Specialist with direct experience in biopharmaceutical QC environments to support automated assay development for cell therapy programs.This role requires hands-on experience in regulated pharmaceutical laboratories, with a strong understanding of GMP ...

We are seeking a Cell Logistics Specialist for a global pharmaceutical client. · Responsibilities include scheduling patient treatment schedules, · serving as point of contact for patient scheduling, · and resolving operational issues related to transportation. · This is a W2 rol ...

We are the largest nonprofit fighting poverty and inequity around the world. Our mission is to create an environment for you to thrive both personally and professionally. · We provide an exceptional benefits package which include comprehensive medical dental vision coverage with ...