Partner Therapeutics

POSITION SUMMARYThe Process Science Department is a group of scientists and subject-matter experts who conduct process and analytical development experiments in support of drug substance and drug product development. This position will work with development scientists in a non-GMP env

POSITION SUMMARYThe Process Science Department is a group of scientists and subject-matter experts who conduct process and analytical development experiments in support of drug substance and drug product development. This position will work with development scientists in a non-GMP env

POSITION SUMMARYManufacturing Associates are involved in cleaning and sterilization of process equipment autoclaving buffer preparation aseptic processing operating process equipment and supporting cGMP operations. Downstream staff focuses on HPLC and low-pressure Chromatography equip

POSITION SUMMARYManufacturing Associates are involved in cleaning and sterilization of process equipment autoclaving buffer preparation aseptic processing operating process equipment and supporting cGMP operations. Downstream staff focuses on HPLC and low-pressure Chromatography equip

POSITION SUMMARYManufacturing Technicians are involved in cleaning and sterilization of process equipment and supporting cGMP operations. The Upstream staff focuses on supporting fermenters and filtration equipment Downstream staff focuses on supporting HPLC and low-pressure Chromatog

POSITION SUMMARYManufacturing Technicians are involved in cleaning and sterilization of process equipment and supporting cGMP operations. The Upstream staff focuses on supporting fermenters and filtration equipment Downstream staff focuses on supporting HPLC and low-pressure Chromatog

POSITION SUMMARYThe Quality Risk & Compliance function establishes and maintains best practices for Quality Risk Management Data Integrity and Audit Readiness to support patient safety product quality and cGMP compliance at PTx. The Quality Risk & Compliance Specialist is responsible

POSITION SUMMARYThe Quality Risk & Compliance function establishes and maintains best practices for Quality Risk Management Data Integrity and Audit Readiness to support patient safety product quality and cGMP compliance at PTx. The Quality Risk & Compliance Specialist is responsible

POSITION SUMMARYThe Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine. These activities include testing raw materials process intermediates Drug Substance (DS) Drug Product (DP) and oversight of all contract laboratory testin

POSITION SUMMARYThe Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine. These activities include testing raw materials process intermediates Drug Substance (DS) Drug Product (DP) and oversight of all contract laboratory testin

POSITION SUMMARYThe Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine. These activities include testing raw materials process intermediates Drug Substance (DS) Drug Product (DP) and oversight of all contract laboratory testin

POSITION SUMMARYThe Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine. These activities include testing raw materials process intermediates Drug Substance (DS) Drug Product (DP) and oversight of all contract laboratory testin

POSITION SUMMARYThe Maintenance Engineering Technician III is a skilled selfdirected technical contributor responsible for the installation troubleshooting and preventive/corrective maintenance of site-wide equipment supporting operations across cGMP manufacturing nonGMP facilities an

POSITION SUMMARYThe Maintenance Engineering Technician III is a skilled selfdirected technical contributor responsible for the installation troubleshooting and preventive/corrective maintenance of site-wide equipment supporting operations across cGMP manufacturing nonGMP facilities an

POSITION SUMMARYThe Maintenance Engineering Technician III is a skilled selfdirected technical contributor responsible for the installation troubleshooting and preventive/corrective maintenance of site-wide equipment supporting operations across cGMP manufacturing nonGMP facilities an

POSITION SUMMARYThe Maintenance Engineering Technician III is a skilled selfdirected technical contributor responsible for the installation troubleshooting and preventive/corrective maintenance of site-wide equipment supporting operations across cGMP manufacturing nonGMP facilities an

POSITION SUMMARYThe Janitor & Clean Room Technician is responsible for performing all routine and specialized cleaning and sanitizing of our biopharmaceutical manufacturing areas in compliance with Good Manufacturing Practices (GMP) and in accordance with Standard Operating Procedures

POSITION SUMMARYThe Janitor & Clean Room Technician is responsible for performing all routine and specialized cleaning and sanitizing of our biopharmaceutical manufacturing areas in compliance with Good Manufacturing Practices (GMP) and in accordance with Standard Operating Procedures