Partner Therapeutics Jobs in United States

A biopharmaceutical company in Seattle seeks a Senior Manager of Automation & Electrical to ensure production efficiency and compliance in a cGMP facility. The role involves leading a diverse engineering team, managing complex automation projects, and ensuring regulatory complian ...

Manufacturing associates are involved in cleaning and sterilization of process equipment, autoclaving, buffer and media preparation, aseptic processing, operating process equipment and supporting cGMP operations. · This position is responsible for performing a variety of manufact ...

The Sr. Manager will lead the Quality Assurance Product Release & Supplier Compliance team at Northpointe site. · ...

The Sr. Manager, Product Release & Supplier Compliance will lead and manage day-to-day activities of the Quality Assurance Product Release and Supplier Compliance teams. · Lead team supporting raw material release.Provide quality review and approval of GMP documentation. ...

This 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 automatio ...

The Regulatory Operations Manager is a regulatory professional with deep regulatory affairs and operations expertise and project management capabilities. · Provides operational oversight and support for planning, preparation tracking publishing QC validation and timely submission ...

Manufacturing Associates are involved in cleaning and sterilization of process equipment, · autoclaving, buffer and media preparation, aseptic processing, operating process equipment and supporting cGMP operations.This position is responsible for performing a variety of manufactu ...

The 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 individual is responsible for assuri ...

This 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 automation ...

The Sr. Manager Product Release & Supplier Compliance 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 individual is responsible for ensuring the quality unit proc ...

The Sr. Manager will lead and manage day-to-day activities of Quality Assurance Product Release teams. · ...

The 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. · Oversight of daily operations of QC PT/CB lab. · Safe, efficient, functional and comp ...

+Job summary · The 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. · +ResponsibilitiesOversight of daily operations of QC PT/CB lab, · Supp ...

Manufac- · turing Associates are involved in cleaning and sterilization of process equipment. · This position is responsible for performing a variety of manufacturing tasks under general guidance and in accordance with current GMPs. · Operates process equipment such as fermenter ...

The 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. · ...

This is a key leadership opportunity for an experienced engineer who thrives at the intersection of technical expertise and team development. · ...

The 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 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. · Primary Quality point of contact for CMOs ...

This is a lab-based role which requires hands-on execution of downstream development, optimization and characterization experiments using small-scale chromatography models. · ...

The 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 deliverables. · Provi ...