Waisman Biomanufacturing

Waisman Biomanufacturing is currently hiring for the role of Quality Control Scientist and will accept applications through Tuesday, November 2nd.

In June, the U.S. Food and Drug Administration approved StrataGraft for the treatment of adult patients with thermal burns. This is the first approved therapy in Waisman Biomanufacturing's book of achievements! Congratulations to everyone involved, past and present, who helped make StrataGraft successful.

FDA Approves StrataGraft for the Treatment of Adults with Thermal Burns FDA approved StrataGraft for the treatment of adult patients with thermal burns containing intact dermal elements

Waisman Biomanufacturing is also hiring for the role of Manager of Operations. Applications will be accepted through Friday, June 25th.

This position will work within the Waisman Biomanufacturing (WB) work unit. WB is a clinical manufacturing facility that produces biologics (gene therapeutics, cell therapeutics, recombinant proteins and vaccines) for Phase I and II Human Clinical Trials in compliance with current Good Manufacturing Practice (cGMP) guidelines. WB's Operations team is responsible for process development, manufacturing, and the specialized equipment and facilities associated with biologics manufacturing. Operations works with Quality Control, Quality Assurance, and Business teams to execute projects for WB's academic and industry clients.

This position will serve as WB's Manager of Operations. The Manager of Operations will research and develop manufacturing processes, develop Standard Operating Procedures (SOPs) for manufacturing operations, oversee validation of manufacturing equipment and processes, train WB manufacturing personnel, and oversee scheduling and ex*****on of operations activities. The Manager of Operations is responsible for oversight of production facilities, including cleaning, maintenance, and validation. After hours response to facilities and equipment alarms is required.

Waisman Biomanufacturing is currently hiring for the role of Quality Assurance Specialist.

This position will work within the Waisman Biomanufacturing (WB) work unit. WB is a clinical manufacturing facility that produces biologics (gene therapeutics, cell therapeutics, recombinant proteins and vaccines) for Phase I and II Human Clinical Trials in compliance with current Good Manufacturing Practice (cGMP) guidelines. The Quality Assurance (QA) Specialist's primary responsibilities will include QA documentation and record keeping, QA raw material control, quality systems (documentation control, failure investigation, deviation reporting, etc.) and training documentation. They will also provide backup support for external audits.

The Pace Of A Pandemic Meets The Speed Of Science As Wisconsin Takes On COVID-19 In Wisconsin, scientists have been in the thick of research into the coronavirus and ways to fight its spread and effects.