Help implement Orca Bio’s global quality management system and support the growth of cell therapy manufacturing.
Posted by employer 3 weeks ago
First seen on Joblaze 1 week ago
Last verified on the company career page 1 day ago
Not disclosed in this posting: compensation, years of experience, work arrangement, visa sponsorship.
Joblaze summary
The Senior Specialist, Global QMS plays a crucial role in implementing and maintaining Orca Bio's global quality management system, focusing on internal audits, supplier management, and inspection readiness. This position requires expertise in GxP compliance and quality systems, as well as strong problem-solving skills to address supplier-related quality issues. Ideal candidates will have a background in quality assurance within the biotechnology or pharmaceutical sectors, particularly at a senior level. Orca Bio is a commercial-stage company dedicated to advancing cell therapies, making this role pivotal in supporting its mission.
From the original posting
More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a commercial-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.
The Senior Specialist, Global QMS will help implement Orca Bio’s global quality management system across all sites. This role will support and lead the internal audit program, supplier management program, and inspection readiness. This role will support the growth and expansion of the global quality program to support manufacturing of our cell therapy products. You will help establish, implement and maintain the audit program across Orca Bio sites to ensure compliance with GxP and regulatory expectations. Your role will support Orca Bios commercial readiness and ongoing clinical programs by managing and facilitating audits, resolving supplier-related quality issues and interacting with quality management teams at the site levels to ensure consistent application of quality systems across the organization.