Laboratory Associate II, GMP - Redwood City

We are searching for motivated individuals interested in advancing science through the manufacturing of our CRISPR regulated products. · Available Shift and Training Schedule: · ...

Synthego is enabling genome engineering at scale with a blend of scientific instrumentation industrial automation and data science. We are searching for motivated enthusiastic and hands-on individuals interested in advancing science through the manufacturing of our CRISPR regulat ...

+Job summary · Synthego is enabling genome engineering at scale with a blend of scientific instrumentation, industrial automation, and data science. · +Operate and verify in the synthesis, purification, and fill/finish operations for clinical grade oligonucleotides by following e ...

· Synthego is enabling genome engineering at scale with a blend of scientific instrumentation, industrial automation, and data science. Our team of scientists and engineers are putting multidisciplinary fields together to solve problems that no one field can tackle alone. · We a ...

The Associate Director, GMP Quality Assurance will play a critical role in providing quality oversight and decision-making authority for commercial manufacturing and batch release activities across Drug Substance (DS), Drug Product Intermediate (DPI), Drug Product (DP), and Comme ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.The Associate Director, GMP Quality Assurance will play a critical role in providing quality oversight and decisi ...

The Associate Director, GMP Quality Assurance will play a critical role in providing quality oversight and decision-making authority for commercial manufacturing and batch release activities across Drug Substance (DS), Drug Product Intermediate (DPI), Drug Product (DP), and Comme ...

The Associate Director, GMP Quality Assurance will play a critical role in providing quality oversight and decision-making authority for commercial manufacturing and batch release activities across Drug Substance (DS), Drug Product Intermediate (DPI), Drug Product (DP), and Comme ...

Our direct client is seeking an Associate Director / Director Quality Assurance to join their growing company. · ...

We are seeking an experienced and strategic Associate Director/Director of CMC Regulatory Affairs to lead and execute regulatory activities for our ECO Synthesis platform and associated manufacturing activities. · Develop and implement CMC regulatory strategies for the ECO Synthe ...

Our start-up Biotech client is seeking an Associate Director / · Director Quality Assurance to join their growing company. · ...

We are seeking an experienced and strategic Associate Director/Director of CMC Regulatory Affairs to lead and execute regulatory activities for our ECO Synthesis platform and associated manufacturing activities. · Develop and implement CMC regulatory strategies for the ECO Synthe ...

We are seeking an experienced and strategic Associate Director/Director of CMC Regulatory Affairs to lead and execute regulatory activities for our ECO Synthesis platform and associated manufacturing activities. · ...

Supports the Quality Assurance (QA) team in maintaining compliance with internal procedures, · regulatory requirements, and quality standards. · Maintains quality documentation including SOPs, training records, and quality records. · ...

+Job summaryAllakos is committed to developing innovative therapies that transform patients' lives. We are looking for bright and talented individuals to join our team and share in our passion and commitment to improving the lives of patients. · +In collaboration with SME, provid ...

We are seeking an experienced and strategic Associate Director/Director of CMC Regulatory Affairs to lead and execute regulatory activities for our ECO Synthesis platform and associated manufacturing activities. · Develop and implement CMC regulatory strategies for the ECO Synthe ...

We are seeking an experienced and strategic Associate Director/Director of CMC Regulatory Affairs to lead and execute regulatory activities for our ECO Synthesis platform and associated manufacturing activities. · - Develop and implement CMC regulatory strategies for the ECO Synt ...

The Opportunity: Quality Assurance Associate. · Maintain compliance with internal procedures and regulatory requirements. · ...

A clinical-stage precision oncology company is seeking a Senior Manager for GMP Quality to lead quality assurance and provide operational support. · Provide QA oversight of process validation activities. · Represent QA on cross-functional teams and serve as a resource for quality ...

Revolution Medicines is seeking a Senior Manager, GMP Quality who will play a key role within Quality Assurance and provide leadership and operational support for RevMed programs through different phases of development. · ...