Partner Therapeutics Jobs in United States

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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 ...

· POSITION SUMMARY · Manufacturing 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 Chrom ...

POSITION SUMMARY · The Sr. Maintenance Engineer is a highly skilled, self‑directed technical contributor responsible for the installation, troubleshooting, and preventive/corrective maintenance of site-wide equipment supporting operations across cGMP manufacturing, non‑GMP facili ...

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 ...

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 ...

· POSITION SUMMARY · The 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 require ...

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

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 ...

· POSITION SUMMARY · The Sr. Maintenance Engineer is a highly skilled, self‑directed technical contributor responsible for the installation, troubleshooting, and preventive/corrective maintenance of site-wide equipment supporting operations across cGMP manufacturing, non‑GMP fac ...

· POSITION SUMMARY · 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 ...

Partner Therapeutics (PTx) is a commercial biopharmaceutical company committed to improving the lives of patients with cancer and other serious diseases. Our dedicated team brings a rigorous approach to science, establishes deep partnerships with medical and scientific communitie ...

· POSITION SUMMARY · The 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 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 ...

POSITION SUMMARY · The 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 h ...

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. ...

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 ...

POSITION SUMMARY · 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 ...

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. · ...

· POSITION SUMMARY · 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 plan ...