Partner Therapeutics

POSITION SUMMARYThe Sr. Maintenance Engineer is a highly skilled selfdirected technical contributor responsible for the installation troubleshooting and preventive/corrective maintenance of site-wide equipment supporting operations across cGMP manufacturing nonGMP facilities and labor

POSITION SUMMARYThe Sr. Maintenance Engineer is a highly skilled selfdirected technical contributor responsible for the installation troubleshooting and preventive/corrective maintenance of site-wide equipment supporting operations across cGMP manufacturing nonGMP facilities and labor

POSITION SUMMARYThe QA Specialist IV External Quality Assurance (ExQA) role is responsible for the overall quality of biologic products and directly involved with CMO oversight of drug substance sterile drug product and finished product manufacturing.). The scope of responsibility can

POSITION SUMMARYThe QA Specialist IV External Quality Assurance (ExQA) role is responsible for the overall quality of biologic products and directly involved with CMO oversight of drug substance sterile drug product and finished product manufacturing.). The scope of responsibility can

POSITION SUMMARYThe Sr. Manager Product Release & Supplier Compliance (Sr. Manager) will be responsible for leading and managing the day-to-day activities of the Northpointe site Quality Assurance Product Release and Supplier Compliance teams. The Sr. Manager will oversee the team sup

POSITION SUMMARYThe Sr. Manager Product Release & Supplier Compliance (Sr. Manager) will be responsible for leading and managing the day-to-day activities of the Northpointe site Quality Assurance Product Release and Supplier Compliance teams. The Sr. Manager will oversee the team sup

POSITION SUMMARYThe QA Specialist IV External Quality Assurance (ExQA) role is responsible for the overall quality of biologic products and directly involved with CMO oversight of drug substance sterile drug product and finished product manufacturing.). The scope of responsibility can

POSITION SUMMARYThe QA Specialist IV External Quality Assurance (ExQA) role is responsible for the overall quality of biologic products and directly involved with CMO oversight of drug substance sterile drug product and finished product manufacturing.). The scope of responsibility can

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 Associates are involved in cleaning and sterilization of process equipment autoclaving buffer and media preparation aseptic processing operating process equipment and supporting cGMP operations. Upstream staff focuses on managing and running fermenters an

POSITION SUMMARYManufacturing Associates are involved in cleaning and sterilization of process equipment autoclaving buffer and media preparation aseptic processing operating process equipment and supporting cGMP operations. Upstream staff focuses on managing and running fermenters 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

POSITION SUMMARYThe Quality Control Analytical Testing group supports the raw material bulk drug substance (API) drug product and in-process monitoring programs of the production facility and support areas. The group supports manufacturing activities at the Northpointe Facility throug

POSITION SUMMARYThe Quality Control Analytical Testing group supports the raw material bulk drug substance (API) drug product and in-process monitoring programs of the production facility and support areas. The group supports manufacturing activities at the Northpointe Facility throug

POSITION SUMMARYThe Regulatory Operations Manager is a regulatory professional with deep regulatory affairs and operations expertise and project management capabilities responsible for leading and contributing to the end-to-end planning coordination and execution of planned deliverabl

POSITION SUMMARYThe Regulatory Operations Manager is a regulatory professional with deep regulatory affairs and operations expertise and project management capabilities responsible for leading and contributing to the end-to-end planning coordination and execution of planned deliverabl

POSITION SUMMARYBIZENGRI is bi-specific antibody that is indicated for patients with non-small cell lung cancer (NSCLC) or pancreatic adenocarcinoma who harbor an NRG1 gene fusion. FDA granted accelerated approval to BIZENGRI in late 2024. Further development is ongoing and the next i

POSITION SUMMARYBIZENGRI is bi-specific antibody that is indicated for patients with non-small cell lung cancer (NSCLC) or pancreatic adenocarcinoma who harbor an NRG1 gene fusion. FDA granted accelerated approval to BIZENGRI in late 2024. Further development is ongoing and the next i

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 is primarily a lab-based role which requires hands-on

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 is primarily a lab-based role which requires hands-on

POSITION SUMMARYThis is a key leadership opportunity for an experienced engineer who thrives at the intersection of technical expertise and team development. The Sr. Manager Automation & Electrical is responsible for hands-on support and troubleshooting as well as leading a team of au

POSITION SUMMARYThis is a key leadership opportunity for an experienced engineer who thrives at the intersection of technical expertise and team development. The Sr. Manager Automation & Electrical is responsible for hands-on support and troubleshooting as well as leading a team of au

POSITION SUMMARYThe Application Systems Administrator III (M365/SharePoint) is responsible for the administration configuration and support of Microsoft 365 and SharePoint Online platforms within a regulated pharmaceutical manufacturing environment. This position ensures that collabor

POSITION SUMMARYThe Application Systems Administrator III (M365/SharePoint) is responsible for the administration configuration and support of Microsoft 365 and SharePoint Online platforms within a regulated pharmaceutical manufacturing environment. This position ensures that collabor