Senior Director, Global Regulatory Lead - Bothell - Immunome

As the Global Regulatory Lead at Immunome, you will be responsible for developing and executing innovative global regulatory strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. · ...

We are looking for a sharp, forward thinking Lead Counsel, Payments and Regulatory to expand our portfolio of financial products. This is an exciting opportunity to build the legal and payments infrastructure to support our cutting-edge financial product stack. · Serve as a trust ...

We are looking for a sharp forward thinking Lead Counsel Payments and Regulatory to expand our portfolio of financial products.This is an exciting opportunity to build the legal and payments infrastructure to support our cutting-edge financial product stack. · You will work close ...

Senior Regulatory Affairs professional with 8+ years of experience in medical devices, specializing in US FDA, EU MDR, and APAC regulations. · ...

+h2>Job summary · Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, drawing on leadership that previously played key roles in the des ...

The Senior Manager Regulatory Operations will play a critical role in leading Immunome’s regulatory systems submissions and documentation processes across our clinical-stage oncology programs. · ...

As part of the Thermo Fisher Scientific team you'll discover meaningful work that makes a positive impact on a global scale Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer · Interpret and ...

We are seeking a Sr. Manager to play a crucial role in interpreting and disseminating global regulations. · Interpret and communicate the impact of relevant global regulations, guidelines, and evolving regulatory trends relating to pharmaceutical product development in the area o ...

The Director Quality Assurance and Compliance is responsible for leading and executing the global quality systems and regulatory compliance strategy for React Health.This position requires managing the planning and implementation of the company quality management system (QMS) as ...

+We are seeking a highly experienced CMC leader to oversee the Chemistry, Manufacturing, and Controls (CMC) strategy and execution for varegacestat. · The ideal candidate will demonstrate strong strategic and operational leadership, ensuring all CMC and product lifecycle delivera ...

About the role method transfer lead scientist is a qc expert within the qcsv group responsible for ensuring that analytical methods are transferred and validated according to cGMP and regulatory expectations. · ...

+Job Summary · We are seeking an accomplished Senior Director, Clinical Development to join our passionate and collaborative team and drive the advancement of our pipeline of targeted cancer therapies. · ...

The Software Design Quality Assurance Engineer is responsible for developing, maintaining and managing comprehensive software quality documentation such as Software Requirement Specifications (SRS), ensuring their accuracy and regulatory compliance throughout the software lifecyc ...

The Method Transfer Lead (MTL), Scientist is a QC subject matter expert within the QCSV group. This individual contributor provides technical leadership to ensure successful execution of method transfer, validation and bridging activities across internal and external laboratories ...

The Associate Director of Quality Operations is responsible for providing strategic and operational QA leadership across assigned programs related to clinical and commercial manufacturing operations with a focus on antibody-drug conjugates ADCs. · Oversee quality aspects of start ...

The Software Design Quality Assurance Engineer is responsible for developing, maintaining and managing comprehensive software quality documentation such as Software Requirement Specifications SRS ensuring their accuracy and regulatory compliance throughout the software lifecycle. ...

This is a QC expert within the QCSV group responsible for method transfer and/or validation to ensure compliance with cGMP and regulatory expectations. · ...

This Senior QC Scientist will lead method transfer and/or validation for assigned programs. They will support project leads internally and externally, author or review protocols and reports, plan and track deliverables. · ...

The Method Transfer Lead (MTL), Scientist, is a QC expert within the QCSV group. This individual contributor has a strong understanding of analytical method transfer and/or validation to ensure that method transfer and/or validation activities comply with cGMP and regulatory expe ...

We're Hiring | Laboratory Operations & Quality Manager EG BioMed US Inc. is a precision medicine and diagnostics company dedicated to advancing innovative clinical testing and early cancer detection. · Quality & Compliance Lead planning implementation maintenance continuous impro ...

+The Senior Manager will lead Immunome's regulatory systems. · +Lead regulatory document submissions. · +Bachelor's degree in scientific discipline required. · ...