This role is responsible for the manufacture of biopharmaceutical analytical reference materials and supports the R&D biopharmaceutical critical reagents program
Job Summary
This role is responsible for the manufacture of biopharmaceutical analytical reference materials and supports the R&D biopharmaceutical critical reagents program.
The position requires managing manufacturing details, scheduling fills, and archiving records to comply with GSK and regulatory requirements.
Candidates will actively prepare for internal quality and external regulatory inspections while supporting large molecule stability teams.
Matching Summary
This role is responsible for the manufacture of biopharmaceutical analytical reference materials and supports the R&D biopharmaceutical critical reagents program.