Mid-Senior CMC Regulatory Writer - Cell Therapy

A leading pharmaceutical company is seeking a mid-senior level Quality - Technical Writer. This contract position involves co-authoring scientific documents for regulatory submissions in cell therapy. Candidates must have a relevant degree and at least two years of experience, along with strong communication skills. The role requires familiarity with eCTD structure and proficiency in Microsoft Office. The successful candidate will work independently and with cross-functional teams to ensure timely delivery of regulatory documentation. #J-18808-Ljbffr