Boehringer Ingelheim Fremont, Inc
The Associate Director regularly leads several process science teams or is the SME on two or more process science functional areas on bioassay and immunoassay development. The primary responsibility of this position is to manage a group (ranging from...
Bulletproof Documentation, Inc.
Bulletproof Documentation, Inc. specializes in high-quality consulting services for the pharmaceutical and medical device industries. With over 20 years of experience, Bulletproof can fulfill your needs on any project, large or small.
Zosano Pharma, Inc.
Zosano Pharma Corporation (ZSAN) is a clinical stage specialty pharmaceutical company that has developed a proprietary transdermal microneedle patch system to deliver drugs through the skin for the treatment of a variety of indications. It offers...
Sutro Biopharma, Inc.
Please submit resume for Req. #1291 to firstname.lastname@example.org.
Sutro Biopharma, Inc. is looking for an energetic and talented individual to join our Manufacturing group. As a Manufacturing Group Leader you will support the manufacturing operations by...
Seattle Genetics, Inc.
Responsible for providing management and technical support of manufacturing projects of Seattle Genetics’ clinical programs. The candidate will primarily support biologics manufacturing projects (antibody, ADC bulk drug substance, and drug product),...
Are you a Process Research and Development Chemist;
with a BS/MS degree in chemistry (required);
and have at least 5 years of related work experience;
with comprehensive experience in cGMP process development.
Do you enjoy practical chemistry...
The Associate Director, Quality Assurance serves a pivotal role in providing Quality leadership and guidance to all corporate functional areas. Under the direction of the head of Quality Assurance, shall be responsible for the design,...
Job Title: Senior Formulation Scientist – Sterile Injectables
Summary: Responsible for formulation and process development activities associated with sterile injectable drug products following Quality by Design (QbD). Technical decision making for...
Supply Chain Management’s areas of responsibility include coordination and management of the procurement, packaging, labeling, distribution, return, reconciliation, and destruction activities of investigational drug supplies
• Facilitates the supply...
The Manager, Regulatory Affairs, CMC will establish and execute regulatory strategies and supporting interactions with regulatory authorities relating to CMC. The manager will plan and coordinate regulatory submissions necessary to...