4/30/2013
ProPharma Group
San Francisco,
CA
ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries. We offer the excitement of a consistently evolving career. Our team is...
4/27/2013
R&D Partners
San Carlos,
CA
Manager/Sr. Manager, Quality Systems
An innovative medical device company is seeking an experienced Quality Manager to oversee the ongoing development and implementation of medical device Quality System.
MAJOR DUTIES AND RESPONSIBILITIES: ...
4/23/2013
Arena Pharmaceuticals, Inc.
San Diego,
CA
Arena Pharmaceuticals, Inc., a leading San Diego-based biotechnology Company, is seeking a candidate for QA DATA SYSTEMS ADMINISTRATOR.
Arena offers an exciting work environment, competitive salary, excellent benefits package, including 401(k) and...
4/23/2013
StemCells Inc.
Mountain View,
CA
StemCells, Inc. is engaged in the research, development, and commercialization of cell-based therapeutics and tools for use in stem cell-based research and drug discovery. The Company’s lead therapeutic product candidate, HuCNS-SC® cells (purified...
4/22/2013
Bulletproof Documentation, Inc.
Burlingame,
CA
Contract/term position providing general project management support for class III medical device development.
Job responsibilities include meeting facilitation, leadership, minutes/agendas, status reporting and management of critical path,...
4/22/2013
Bulletproof Documentation, Inc.
South San Francisco,
CA
• Create (from-scratch) and/or significantly rewrite documents including but not limited to design history files, design verification records, and master production records.
• Master technical information, organize content, and imbed GxP compliance
•...
4/18/2013
Kyowa Hakko Kirin Ca, Inc.
La Jolla,
CA
Summary: QA Specialist is responsible for implementing, managing, and directing the Quality Assurance Program for a Laboratory that provides bioanalytical services including sample management, method development, method validation, and clinical...
4/17/2013
Gilead Sciences
Oceanside,
CA
Performs a wide variety of activities to ensure compliance with applicable regulatory requirements. Participates in developing Standard Operating Procedures to ensure quality. Maintains programs and processes to ensure high quality products and...
4/17/2013
Gilead Sciences
Oceanside,
CA
Supervises QA Documentation Specialist(s), including organizing and prioritizing daily tasks, performing training, and writing performance reviews. Responsible for coordinating all activities related to providing required documentation and...
4/17/2013
Cellerant Therapeutics, Inc.
San Carlos,
CA
Cellerant Therapeutics, Inc. is a product focused biotechnology company with a portfolio of development stage programs based on the regulation of the hematopoietic (blood-forming) system. The Company focuses on human stem cell and antibody therapies...