Our Strength Is Our People. Passion. Principles. Perspective.At Actavis Inc., these are the traits that drive our growth and we apply them to every project and product. If you bring these qualities to your work, then we'd like you to consider joining...

This is a full-time position in the Process Development group reporting to the head of cell culture and cell line development. The candidate's responsibilities will include performing transient and stable transfections of mammalian cells for protein...

Astute Medical, Inc., an innovative in vitro diagnostic company, is seeking a Laboratory Supervisor to join our product development team. The Laboratory Supervisor is responsible for leading a team of up to five employees who produce and test...

Responsible for the support of Infectious Disease and Molecular Controls Manufacturing, including planning, scheduling and executing validation. Responsible for process engineering, process improvement, product transfer and scale up of...

•May supervise a small to medium function. •Receives general instructions. •Determines work assignments and priorities. •Supervises production according to established protocols •Coordinates establishment and documentation of procedures. Ensure SOPs...

Calling all Biotech, Pharma, and Medical Device Professionals! Pharm Country Career Fair Radisson Valley Forge Tuesday, May 21, 2013 11am - 4pm Exhibiting companies include: Accenture Aerotek Galderma Research & Development, Inc. University of...

Biotech Bay Career Fair San Francisco Airport Waterfront Marriott Thursday, June 6, 2013 1pm to 6pm EXHIBITING COMPANIES Bayside Solutions, Inc. California Applied Biotechnology Centers Initiative Integrated Project Management More To Come!!!

Collaborate with the VP CMC Operations to ensure Project goals are met, and CMC systems are created, documented, and maintained. Work with CMC Service Providers to 1) ensure the quality manufacture of drug substances and products for their intended...

• 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 •...

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,...