•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...

Lead and direct the activities of Analytical Development department in the Nektar Pharmaceutical Development and Manufacturing organization. Responsible for product characterization, analytical method development, process development support and...

Supports the PU in all process-specific issues, drives continuous process improvement for quality and quantity and ensures GMP requirements are met and guidelines and SOPs are followed. Provide continuous supply of high quality products that meet...

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...

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...

Fantastic opportunity to lead the Commissioning and Qualifications activities for a state of the art GMP Biologics facility. Come join an experienced and highly respected Engineering leadership team at a top biopharmaceuticals company in the Boston...

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...

Summary & Scope of Position: Technical lead for Chemistry, Manufacturing, and Controls (CMC) activities for INTERCEPT Blood Systems for Platelets, Plasma, and Red Blood Cells. Scope includes support for new product development, product...

Novartis in San Carlos is seeking a Process Unit Engineer Responsible for availability and reliability of equipment and instruments in the Process Unit. Drives preventive maintenance and calibration. Ensures modification to equipment is carried out...

• 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 •...