Deviation Writer Position Available In Johnston, North Carolina
Tallo's Job Summary: A global pharmaceutical manufacturer is hiring a Deviation Writer to conduct investigations and processes related to aseptic production. The role requires 2+ years of pharmaceutical experience in a GMP setting, as well as experience in CAPA and Root Cause Analysis. This M-F, 1st shift role involves technical writing and collaboration with production teams.
Job Description
Job Title:
Deviation Writer Job Description A global pharmaceutical manufacturer is seeking a Deviation Writer. This individual will conduct investigations and processes. Responsibilities include performing historical searches, watching videos, interviewing colleagues, reviewing supporting documentation (batch records, technical assessments, SOPs, etc.), and housing this information in a proprietary system. Responsibilities Conduct investigations specific to processes. Perform historical searches and watch videos related to aseptic production. Interview colleagues to gather information. Review supporting documentation such as batch records, technical assessments, and SOPs. Utilize and maintain information in a proprietary system daily. Essential Skills Previous pharmaceutical experience in a GMP commercial setting. 2+ years of experience in Aseptic Manufacturing within a pharmaceutical environment. Experience conducting investigative processes, CAPA, and Root Cause Analysis. Systematic problem-solving skills with exposure to root cause analysis, investigative process, technical writing, or CAPA. Technical writing experience, including writing technical documents and CAPA reports. Additional Skills & Qualifications Root Cause Analysis CAPA Technical Writing Process Improvement Work Environment This is a normal M-F, 1st shift opportunity. It is a cross-functional role within an office space and involves partnering with production on the floors.