ASSOCIATE DIRECTOR DIRECTOR DRUG jobs in SAN FRANCISCO CA UNITED, United Kingdom

and company culture, visit us at | Who You Are The Senior Manager/Associate Director, Drug Substance Development... clinical study and has received Orphan Drug and Fast Track Designations from the US FDA. BridgeBio is a biopharmaceutical...

with a strong background in final drug product (FDP) development and manufacturing in the biopharmaceutical industry. This role works with the.../commercial drug product operations with a focus on effective troubleshooting, interfacing with existing teams to collaboratively...

forward. For more information, please see . Position Summary: We are seeking an experienced and highly motivated Associate Director / Director... and scientists, including direct reports or supporting team members The salary range for this position at the Associate Director...

of. Scientific Associate Director - Inflammation Live What you will do Let’s do this. Let’s change the world. In this vital... of drug discovery experience OR Master’s degree and 7 years of drug discovery experience OR Bachelor’s degree and 9 years...

's housing crisis in an innovative way? Home Match is seeking an Associate Director for our San Francisco office to help lead... dynamic for the lifetime of their match. www.frontporch.net/homematch Summary The Associate Director of San Francisco...

The Genentech Corporate Law team is seeking to hire a Practice Group Leader, Senior Director & Associate General... on regulatory and compliance matters arising under the Federal Food, Drug, and Cosmetic Act related to manufacturing practices (cGMP...

. Manager/Associate Director, Market Access Marketing to support the tactical execution of the Market Access strategies... in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage...

tomorrow’s most innovative cancer therapies. Abdera is seeking an Associate Director, Clinical Quality Assurance, to lead clinical quality... for Abdera’s novel oncology therapy clinical programs. The Associate Director of Clinical Quality Assurance will be responsible...

Frontier Medicines is seeking a highly motivated individual for a newly created Associate Director role in Process... from process chemistry development through to drug substance manufacturing. Requirements What will you be doing? Responsible...

of. Scientific Associate Director – Translational Pathology Live What you will do Let’s do this. Let’s change the world. The... our drug development programs and is accountable for the development of biomarker and diagnostics strategy across our pipeline...

and company culture, visit us at | Who You Are The Sr. Clinical Trial Manager/Associate Director manages the operational... delivery of meaningful medicines to patients. Founded in 2015, the company has built a portfolio of 30+ drug development...

, California. Overview The Associate Director/Director, GCP Quality Assurance oversees GCP activities at Nkarta, our CROs... trials from first in human through commercial marketing authorization by Health Authorities for of our cellular therapy drug...

to delivering effective therapies to patients. The Opportunity We are currently seeking an outstanding Associate Director... which includes drug dosing in mice and rats by various routes of administration (IV, PO, IP, SQ, RO, IT), in life sample collections...

Associate Director/Director, Statistical and Translational Genomics About Foresite Labs Foresite Labs... We are looking for an experienced applied statistical geneticist to join our team as an Associate Director to support the development and testing...

Join Frontier Medicines on an exciting journey as our newest Principal Scientist/Associate Director, Process Chemistry... development and manufacturing of drug substances, overseeing both internal and external resources, and collaborating closely...

with focus on both large and small molecules. Experience of releasing or supporting release of clinical or commercial drug... substance & drug product. Current and strong working knowledge of 21 CFR Parts 210-211 and 11; EU cGMP/GLPs; and ICH quality...

portfolio including process development and manufacture of regulatory starting materials (RSMs) and support production of Drug... to support candidate selection during drug discovery, from preclinical development through commercialization Identification...